Synthetic biology

Those familiar with academia know that disputes over trademarks can be more intense (and, in a prurient sense, more interesting) than disputes over substance. Synthetic biology has such a dispute in the making.

The title 'synthetic biology' appeared in the literature in 1980, when it was used by Barbara Hobom to describe bacteria that had been genetically engineered using recombinant DNA technology¹. These bacteria are living systems (therefore biological) that have been altered by human intervention (that is, synthetically). In this respect, synthetic biology was largely synonymous with 'bioengineering'.

In 2000, the term 'synthetic biology' was again introduced by Eric Kool and other speakers at the annual meeting of the American Chemical Society in San Francisco². Here, the term was used to describe the synthesis of unnatural organic molecules that function in living systems. More broadly in this sense, the term has been used with reference to efforts to 'redesign life'^3,4,5. This use of the term is an extension of the concept of 'biomimetic chemistry', in which organic synthesis is used to create artificial molecules that recapitulate the behaviour of parts of biology, typically enzymes⁶. Synthetic biology has a broader scope, however, in that it attempts to recreate in unnatural chemical systems the emergent properties of living systems⁷, including inheritance, genetics and evolution^3,4,5,8. Synthetic biologists seek to assemble components that are not natural (therefore synthetic) to generate chemical systems that support Darwinian evolution (therefore biological). By carrying out the assembly in a synthetic way, these scientists hope to understand non-synthetic biology, that is, 'natural' biology. This motivation is similar in biomimetic chemistry, where synthetic enzyme models are important for understanding natural enzymes.

More recently, an engineering community has given further meaning to the title. This community seeks to extract from living systems interchangeable parts that might be tested, validated as construction units, and reassembled to create devices that might (or might not) have analogues in living systems⁹. The parts come from natural living systems (that is, they are biological); their assembly is, however, unnatural. Therefore, one engineering goal might be to assemble biological components (such as proteins that bind DNA and the DNA sequences that they bind) to create, for example, outputs analogous to those of a computer.

A common ground between the 'synthetic biology' and engineering communities lies in the global strategy by which scientists come to understand their subject matter, make discoveries and overturn paradigms. Synthesis offers opportunities for achieving these goals that observation and analysis do not. The use of synthesis in a way that complements analysis will be a main theme of this review (Box 1).

Synthetic biology already has many accomplishments to its credit. The effort to generate synthetic genetic systems has yielded diagnostic tools, such as Bayer's branched DNA assay (described in a later section), which annually helps improve the care of some 400,000 patients infected with HIV and hepatitis viruses^10,11,12. These and other artificial genetic systems now support primitive genetic processes, including replication with the possibility of mutation^13,14, selection¹⁵ and evolution. Synthetic biology has also generated some interesting toys from biomolecular parts, including systems that oscillate¹⁶ and that carry out simple computations¹⁷.

For engineering purposes, parts are most suitable when they contribute independently to the whole. This 'independence property' allows one to predict the behaviour of an assembly. Therefore, it makes sense to structure this review to follow the search for independently interchangeable parts.

This search turns out to be interesting. In molecular science, it is well known that the simplest building units (the atomic parts) do not always contribute independently to the behaviour of a molecular assembly (the whole). In the macroscopic physical world, building units often do, especially if they are designed to do so (as in modular software assembly, for example). Ultimately, synthetic biology succeeds or fails as an engineering discipline depending on where independence approximations become useful in the continuum between the atomic and macroscopic worlds.

As a science, synthetic biology can be evaluated in different ways. By measuring the insights, discoveries and paradigm shifts that are driven by synthetic biology, we ask here whether the synthetic approach has contributed in a way that is not easily possible by analysis alone.

Seeking interchangeable parts: DNA

As described by Watson and Crick 52 years ago, DNA has a modular structure. In a reductionist sense, DNA can be described as two antiparallel strands. Each strand is assembled from four different nucleotide building blocks, which are themselves assembled from sugars, phosphates, and nucleobases. These are, in turn, assembled from carbon, nitrogen, oxygen, phosphorus and hydrogen atoms.

In the Watson–Crick model, nucleotide pairs contribute independently to the stability of a duplex. In reality, this is a good approximation. DNA duplexes can be designed with considerable success by applying just two rules: A pairs with T, and G pairs with C. A second-order model does very well by adding only the effect of adjacent base pairs into the calculation¹⁸. Although some diversity in nucleic acid structure and function is not captured by such simple rules (for example, that of Z-DNA¹⁹, G QUARTETS²⁰, and catalytic RNA²¹), most molecular biologists only use this diversity occasionally.

The elegance of the Watson–Crick model has caused most molecular biologists to overlook the chemical peculiarity of such rules. No other molecular system can be described so simply. For example, the behaviour of a protein is generally not a transparent function, linear or otherwise, of the behaviours of its constituent amino acids, even as an approximation. The power of the Watson–Crick rules was nevertheless sufficient to lead to complacency by most of those who learned the double helix structure; molecular recognition in DNA was a 'solved problem'.

The role of the DNA backbone in molecular recognition. This complacency was only dislodged through synthesis of nucleic acids. Starting in the 1980s, some synthetic biologists began to wonder whether DNA and RNA were the only molecular structures that could support genetics on Earth or elsewhere^3,22,23. Other biologists, seeking technological goals, attempted to replace modules in the DNA structure to create DNA analogues that would, for example, passively enter cells, but could still support the 'A pairs with T, G pairs with C' rule, with the aim of disrupting the performance of intracellular nucleic acids in a sequence-specific 'antisense' way²⁴.

This antisense idea was simple in cartoon form. The phosphate backbone was thought to be largely responsible for the unsuitability of DNA as a drug: the repeating backbone phosphates prevented nucleic acids from partitioning into lipid phases, an event believed to be essential for molecules to enter cells passively. The phosphate–ribose backbone is also the recognition site for nucleases. This knowledge, and the fact that the Watson–Crick model proposed no particular role for the phosphates in molecular recognition, encouraged the inference that the backbone could be changed without affecting pairing rules.

The effort to synthesize non-ionic backbones changed the established view of nucleic acid structure. Nearly 100 linkers were synthesized to replace the 2′-deoxyribose sugar, starting with the first by the Pitha²⁵ and Benner²⁶ laboratories. Nearly all analogues that lacked the REPEATING CHARGE showed worse rule-based molecular recognition. Even with the most successful uncharged analogues (such as the polyamide-linked nucleic-acid analogues (PNA) created by Nielsen and his group²⁷) molecules longer than 15 or 20 building units generally failed to support rule-based duplex formation. In other uncharged systems, the breakdown occurs earlier²⁸.

This discovery was unfortunate for the antisense industry, but it had a marked effect on our understanding of DNA. The repeating charge in the DNA backbone could no longer be viewed as a dispensable inconvenience. The same is true for the ribose backbone of RNA: although several backbones (such as THREOSE DNA or LOCKED NUCLEIC ACIDS) work as well or better than ribose^24,29,30, most of the replacements work less well. The backbone is not simply scaffolding to hold the nucleobases in place; it has an important role in the molecular recognition that is central to genetics.

Evolution of genetic molecules. The above example illustrates how synthesis drives discovery and paradigm change. The failure to obtain non-ionic DNA analogues that retain rule-based pairing led scientists to think about the chemical structures that might be needed to support Darwinian evolution.

In particular, a genetic molecule must be able to suffer change (mutation) without markedly changing its overall physical properties. Again, this feature is infrequent in chemical systems (in proteins, for example). But because charge dominates the physical properties of a molecule, a repeating charge should allow appendages (the nucleobases, in the case of DNA and RNA) to be replaced without changing the dominant behaviour of a genetic system³¹. This has led to the suggestion that a repeating charge might be a universal feature of genetic molecules that work in water³¹.

Furthermore, the discovery that ribose was one of the better backbone sugars for supporting molecular recognition^24,32 had implications for the origin of life on Earth. In the mid 1990s, Miller had commented that because of the ease with which ribose decomposes as a sugar on heating³³, ribose could not have supported the first genetic system on Earth. The results from synthesis, which indicated that ribose is especially good for genetics, drove efforts to find prebiotic routes to ribose that would overcome its intrinsic instability^34,35.

Creating synthetic genetic systems. Synthesis focusing on the nucleobases also generated discoveries. The Watson–Crick pairing rules arise from two rules of chemical complementarity. The first, size complementarity, pairs large purines with small pyrimidines. The second, hydrogen-bonding complementarity, pairs hydrogen-bond donors from one nucleobase with hydrogen-bond acceptors from the other.

If nucleobase pairing were indeed so simple, it should be possible to move atoms around within the nucleobases (on paper) to synthesize unnatural nucleobases that would still pair following rules of size and hydrogen bonding complementarity, but differently from the natural nucleobases. Indeed, by shuffling the hydrogen-bond donating and accepting groups, one can easily generate eight additional synthetic nucleobases, forming four additional base pairs (Fig. 1).

Parts of the nucleobases of DNA can be used as interchangeable building modules. The blue units are the hydrogen bonding donor (D) collections of atoms. The red units are the hydrogen bonding acceptor (A) collections of atoms. a | The four standard nucleobases are shown. b | Shuffling the hydrogen bond donor and acceptor modules generates eight additional nucleotides, which constitute a synthetic genetic system. These synthetic bases have been used in an artificial genetic system that can support Darwinian evolution. A, adenine; C, cytosine; G, guanine; Pu, purine; Py, pyrimidine; T, thymine.

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In this case, synthesis showed that nucleobase pairing is as simple as the Watson–Crick model implies. A synthetic genetic alphabet with up to 12 independently replicatable nucleobase pairs can be supported by an extended set of Watson–Crick rules³⁶. Furthermore, a small amount of protein engineering converts natural polymerases into polymerases that accept components of an expanded genetic alphabet in a polymerase chain reaction¹⁴. This created, for the first time, a synthetic genetic system that can be repeatedly copied, with the level of mutation needed to support adaptation and evolution.

By searching for synthetic systems that could recreate such emergent properties, synthetic biologists have discovered a great deal. For example, it was proposed that DNA polymerases scan the minor groove of a DNA duplex to look for unshared pairs of electrons as a recognition feature³⁷. It was likewise proposed that this scanning of the minor groove was essential for the high fidelity of DNA replication. Efforts to obtain polymerases to support the evolution of the artificial genetic system led to the discovery that minor-groove scanning is not an essential feature of all polymerases.

Today, the effort to make a synthetic chemical system that is capable of Darwinian evolution is an important focus of the National Science Foundation's Chemical Bonding Program. Here, the details of the chemical structures of nucleobases that are essential to support genetics have been determined, with the goal of repairing specific chemical problems that limit the use of specific components of an expanded genetic alphabet. For example, several components of an artificial genetic system suffer from EPIMERIZATION; this has been rectified by adding nitro substituents to the nucleobases³⁸. Another component of the artificial system, iso-guanosine, has a minor TAUTOMERIC form that cross bonds with thymidine, creating a significant number of mutations in polymerase chain reactions. This defect was solved by replacing a nitrogen in the structure by a carbon atom³⁹.

Because it provides rule-based molecular recognition that is orthogonal to the recognition provided by natural DNA, this synthetic genetic system is found today in the clinic. As part of the Bayer VERSANT branched DNA diagnostic assay⁴⁰, synthetic biology helps to manage the care of approximately 400,000 patients infected with HIV and hepatitis viruses each year^10,11(Fig. 2).

The target RNA molecule to be detected (the analyte) is attached to the plastic of a microwell (bottom) by the hybridization of the analyte to a series of capture probes. This complex then captures, through hybridization, a target probe, which in turn hybridizes to a pre-amplifier molecule, thereby 'sandwiching' the analyte between the capture probe and the pre-amplifier. The pre-amplifier captures a branched DNA dendrimer (amplifier) that contains several signalling molecules on each branch. As a consequence of the branching, a single analyte assembles a large number of signalling molecules in the microwell. These assays use the expanded genetic alphabet shown in Fig. 1. When standard nucleotides were used to assemble the signalling nanostructure, significant noise was seen, because non-target DNA that was present in the biological sample was captured by the probes in the microwell even in the absence of analyte. Incorporating components of the artificial genetic alphabet in the dendrimer reduced the noise. As a consequence, the assay now helps manage the care of some 400,000 patients annually, detecting as few as eight molecules of the analyte DNA in a sample.

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Seeking interchangeable parts: proteins

The amino acid as a building module in proteins. The synthetic biology of nucleic acids is successful because the repeating charge in the backbone enables the nucleotide parts to be exchanged independently (although we acknowledge the fact that some RNA structures, such as G-rich sequences, are themselves problematic to engineer). Proteins, unfortunately, do not have a repeating charge; engineering them has therefore been more difficult.

Proposals to engineer proteins, for which the interchangeable unit is the amino acid, is as old as recombinant DNA technology^41,42. This idea was discussed in an engineering context in 1983 by Kevin Ulmer, then director of exploratory research at Genex⁴³. In Ulmer's vision, synthetic biologists would first alter the behaviours of proteins by replacing amino acid BUILDING MODULES in the natural proteins. The replacements would come from the standard set of 20 natural amino acids, and would be chosen using primitive design principles to meet specific goals defined by the properties desired in the synthetic protein. Such primitive principles might, for example, place charged residues at the top and bottom of α helices, or strategically alter amino-acid size complementarity in the active site of an enzyme.

Design based on such primitive rules was expected to frequently fail. Failure, however, would drive the development of better design rules⁴⁴. This would generate a cycle, involving the setting of a goal, the replacement of amino acids to create proteins to meet the goal using the improved design rules, followed by success and failure, refinement of the design rules, and the setting of new goals. This process might go on for decades, and perhaps even generate some of the emergent properties that characterize biological systems. This vision remains largely unrealized. The 20 years of experience since Ulmer presented his vision has shown that the behaviour of a protein is not a simple combination of independent contributions from the constituent amino acids⁴⁵.

The failure of the independence approximation was, in large part, expected⁴⁶. First, amino acids in a folded polypeptide sequence strongly interact with others, even amino acids distant in the polypeptide chain⁴⁷. More seriously, even the simplest of molecular interactions are poorly understood. Today, chemical theory still cannot retrodict the freezing point of water⁴⁸, the solubility of simple salts in water⁴⁹, or the packing of crystals of simple organic molecules⁵⁰. Protein folding is, in one view, an aggregate of these particular processes. A theory that cannot manage the particulars is not expected to manage the whole. Nevertheless, the synthetic effort will be crucial for demonstrating and overcoming these limitations of theory.

Serious efforts are under way to improve the computational tools needed to design and engineer proteins^51,52,53. Some have attempted to improve design principles by examining ROTAMERS of amino acids, where different arrangements of side-chain atoms are used as the building modules, rather than the amino acids themselves⁵⁴. Small protein folds have focused the simplification of design issues⁵⁵. These include elegant examples from the laboratories of Imperiali, Allemann and Mayo.

Today, the technology of amino-acid replacement is done using a combination of calculation, design, screening, selection, and luck⁵⁶. Even so, the outcome has been positive⁵⁷; many useful enzymes have emerged by means of amino acid replacement, including polymerases used for DNA sequencing⁵⁸, reverse transcriptases that use PCR to amplify synthetic genetic systems¹⁴, and enzymes in commercial laundry detergents⁵⁹. But these are far from a synthetic biology that captures the emergent properties of living systems.

The protein-folding unit as the building module. Proteins are built from secondary structure units, including the α helix and the β strand⁶⁰. This gave rise to the idea that such secondary structural elements might serve as interchangeable parts to support protein design⁶¹.

Kaiser and his many students have been especially successful in using the amphiphilic helix as the interchangeable building unit. In an amphiphilic secondary structure, hydrophobic and hydrophilic amino-acid side chains are arranged in the sequence so that a hydrophilic side of the unit can face water, while a hydrophobic side can be buried in the protein fold. Such amphiphilic structures are expected to pack spontaneously in water.

Using this strategy, DeGrado et al. designed an artificial polypeptide that reproduced some of the folding and biological properties of mellitin, a protein from the sting of a bee, without reproducing its exact sequence⁶². The designed peptide was amphiphilic, and the model proposed that its hydrophobic side buries itself in the hydrophobic membrane of a cell. Amphiphilic helices as units have frequently been exploited since then⁶³. Analogous approaches have used the β strand as the architectural module⁶⁴.

Several laboratories have worked to create emergent biological properties, including templated replication, by using secondary structural elements as interchangeable building modules. For example, the Ghadiri laboratory designed a peptide by assembling α helical coiled coils to obtain a peptide ligase⁶⁵ and a peptide replicator⁶⁶ (Fig 3).

a | A de novo designed peptide ligase. α-helical peptides A and B bind to the electrostatically complementary α-helical peptide C to form the C·A·B ternary complex, which is composed of two coiled coils. Peptide A has a modified amino terminus that reacts with the chemically modified carboxyl terminus of peptide B on formation of the ternary complex. The reaction of peptides A and B is a ligation that forms the product C·P (C·P^* represents the chemical reaction between A and B to produce P). b | Peptide replicator schematic based on the reaction illustrated in part a, showing the reaction of peptide A with peptide B on formation of a ternary complex with peptide C. Peptides A^L, B^L, and C^LL are composed of L-amino acids, whereas peptides A^D, B^D, and C^DD are composed of D-amino acids. Peptides C^LL and C^DD are produced autocatalytically in a template-directed fashion through the reaction of precursors A^L with B^L, and A^D with B^D, respectively. Therefore, this replicator is stereochemically selective, only producing products (C^LL and C^DD) that are isomerically pure. Part b modified, with permission, from Ref. 65 © American Chemical Society (2001) and from Nature Ref. 66 © (2001) Macmillan Magazines Ltd.

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Much of this work falls squarely within the definition of biomimetic chemistry, in that it reproduces isolated behaviours of natural biological systems. This includes using amphiphilic helices as design elements to create a synthetic enzyme that catalyzes the decarboxylation of oxaloacetate⁶⁷. Further work with modular design has improved this artificial enzyme⁶⁸. A wide range of catalytic activities are now being sought in this fashion based on the modular assembly of secondary structure building units. These include artificial enzymes that catalyze ester hydrolysis⁶⁹, oxidize phenol using molecular oxygen⁷⁰ and catalyze aldol reactions⁷¹.

Despite these successes, helices and strands remain challenging as building modules to support synthetic biology in proteins. Even when amphiphilic elements assemble in water to form a fold, the interior packing is often dynamic (a 'molten globule'). Subsequent design, trial and luck are required to refine the dynamic core to make it rigid. More trivially, many protein design projects have failed simply because proteins have a tendency to precipitate. The backbones of proteins do not carry a repeating charge (like nucleic acids do); instead, the repeating unit is a dipole (the amide linkage), which is well suited for self-aggregation. Much of protein design, therefore, is an effort to design peptides that remain dissolved in water.

It has been suggested that natural selection might have used secondary structural elements as interchangeable parts in constructing new proteins. Vestiges of such swapping might be detectable in very ancient steps for the construction of proteins⁷². But the recent widespread recruitment of function (proteins that share 50% sequence identity can catalyze very different reactions⁷³) seems to have arisen primarily through point mutation, insertion and deletion.

The natural protein as the engineering unit. As we move from the atomic to the macroscopic world, the next step considers folded proteins as interchangeable parts. The biosphere contains proteins that have a wide diversity of physical and catalytic properties. For several decades, metabolic engineers have asked whether these can be reassembled as building modules to create new pathways that capture at least some of the emergent properties of biological systems. This might be done without needing to solve the difficult problem of constructing artificial proteins from scratch.

The simplest idea behind metabolic engineering has been to simply redirect the metabolism of a cell by altering its genetic makeup⁷⁴. This has long been achieved by non-rational means; fermentation strains obtained by classical screening and selection are widely used in industry (in the synthesis of citric acid, for example)⁷⁵. The advent of recombinant DNA technology has led to enhanced efforts to pick and choose enzymes from a range of organisms and then to assemble these enzymes into a single organism to produce products that might not be native to the organism. For example, Fukui et al.⁷⁶ constructed a strain of the bacterium Ralstonia eutropha that was able to produce poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) from fructose (Fig. 4a). The strain was engineered by introducing genes for various steps in the pathway from two other microorganisms in addition to R. eutropha.

a | The combination of enzymes from three sources in a Ralstonia eutropha host generated a strain that produced large amounts of a poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) polymer from fructose. All enzymes from Ralstonia eutropha are shown in black, whereas those from Areomonas caviae and Streptomyces cinnamonensis are shown in green and red, respectively. Modified, with permission, from Ref. 76 © American Chemical Society (2002). b | The combination of enzymes from three sources in an Escherichia coli host generated a strain of the bacterium that produced a precursor for artemisinin, an antimalarial drug. The challenge of this experiment lay in the need to curtail the pathway to recognize and avoid metabolite toxicity, while optimizing the yield of the desired product. The general methodology for the pathway design was to use an engineered mevalonate pathway that is absent in E. coli, rather than the DXP (1-deoxy-D-xylulose 5-phosphate) pathway that is native to the organism. The synthetic operons used are depicted, and the engineered pathway metabolites are shown in red. In the engineered mevalonate pathway, the fan of genes from ERG12 to ispA exist on multiple plasmids to tune the pathway for optimization of the product while avoiding metabolite toxicity. As depicted at the bottom of the figure, the E. coli strain DYM1, a strain deficient in isoprenoid synthesis, was used, because the DXP pathway was found to limit product yield, probably owing to an unrecognized link between the pathway and physiological control elements in the organism. Enzymes used (isolated from Saccharomyces cerevisiae unless otherwise noted): ADS, amorphadiene synthase; atoB, acetoacetyl-CoA thiolase (E. coli); dxs, 1-deoxy-D-xylulose 5-phosphate synthase; ERG12, mevalonate kinase; ERG8, phosphomevalonate kinase; HMGS, HMG-CoA synthase; idi, IPP isomerase (E. coli); ippHp, IPP isomerase (H. pluvialis); ispA, FPP synthase (E. coli); ispC, 1-deoxy-D-xylulose 5-phosphate reductoisomerase; MVD1, mevalonate pyrophosphate decarboxylase; tHMGR, truncated HMG-CoA reductase. Pathway intermediates: AA-CoA, acetoacetly-CoA; A-CoA, acetyl-CoA; CDP-Me, 4-diphosphocytidyl-2-C-methyl-D-erythritol; CDP-ME2P, 4-diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate; DMAPP, dimethylallyl pyrophosphate; DXP, 1-deoxy-D-xylulose 5-phosphate; FPP, farnesyl pyrophosphate; G3P, glyceraldehyde 3-phosphate; HMB4PP, 1-hydroxy-2-methyl-2-(E)-butenyl 4-pyrophosphate; HMG-CoA, hydroxymethylglutaryl-CoA; IPP, isopentenyl pyrophosphate; Mav-P, mevalonate 5-phosphate; ME-2,4cPP, 2-C-methyl-D-erythritol 2,4-cyclopyrophosphate; MEP, 2-C-methyl-D-erythritol 4-phosphate; Mev-PP, mevalonate pyrophosphate. Adapted, with permission, from Nature Biotechnology Ref. 77 © (2003) Macmillan Magazines Ltd.

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An analogous example comes from the Department of Synthetic Biology at the division of Physical Biosciences at the Lawrence Berkeley National Laboratory⁷⁷. Here, researchers developed a strain of Escherichia coli that could synthesize amorphadiene, an isoprenoid precursor for the antimalarial drug artemisinin. The pathway combined the acetoacetyl-CoA thiolase (encoded by the atoB gene) from E. coli, an isopentenylpyrophosphate isomerase from Haematococus pluvialis, and several enzymes from Saccharomyces cerevisiae (Fig. 4b). The Gates Foundation is now funding the scaling up of this process as part of its mission to generate inexpensive drugs for the third world.

As Khosla and Keasling noted⁷⁸, metabolic engineering generally requires more than simply throwing enzymes together in a cell. Achieving a synthetic goal (here, a strain that produces a particular product) requires the management of complex metabolic and regulatory processes. In pursuit of this goal, one cannot help but learn about metabolism and its emergent behaviours, including the regulation of metabolism and the extent to which enzymes drawn from various sources can be combined independently. So, synthesis drives discovery and learning.

Using genes and genetic elements. One way to search for interchangeable parts is to identify the parts that are used in natural evolution. The archetypal example of modularity in evolution is found in genetic regulatory and signalling pathways. Here, combinations of proteins often function as molecular switches, that is, they are stimulated by upstream events (ligand binding, a chemical reaction, or the movement of components into new locations) and generate an output, which can then serve as an input for another switch. Recruitment and the exchange of individual proteins in such pathways throughout eukaryotic evolution has generated many logical networks that control cellular behaviour⁷⁹.

Given this natural precedent, one goal for synthetic biology is to take the proteins themselves as building modules and synthesize artificial regulatory circuits that have preselected inputs and outputs. As before, the motivation is not so much to construct 'toys', but rather to use the challenge of a synthetic goal to discover principles that connect the chemistry of signal transduction to emergent regulatory properties in complex biology.

Several examples show how this might be done. In signal transduction pathways that involve receptor tyrosine kinases, tyrosine-containing motifs are autophosphorylated. These then dock to the Src homology 2 (SH2) and phosphotyrosine-binding (PTB) domains of adaptor proteins, which, in turn, activate signalling pathways that generate specific cellular responses. The signal created by these events depends on the details of the adaptor proteins. For example, the SH2 domain of the growth factor receptor-bound protein 2 (GRB2) adaptor is flanked by two Src homology 3 (SH3) domains. These bind proteins, such as the guanine nucleotide exchange factor son of sevenless homolog 2 (SOS2) and GRB2-associated binding protein 1 (GAB1) docking protein, which then help to activate the Ras and phosphatidylinositol 3'-kinase pathways, respectively. GRB2 therefore couples the phosphorylated motifs to signalling pathways that lead to cell survival, growth and proliferation. Different combinations lead to the opposite outcome. For example, autophosphorylated death receptors bind adaptors, such as fas (TNFRSF6)-associated via death domain (FADD); this is followed by an analogous signalling process that promotes cell death through apoptosis.

In an intriguing study from Pawson's group⁸⁰, growth-promoting and death-promoting modules were rearranged. In this work, the phosphotyrosine recognition domains of GRB2 — either SH2 domain or ShcA phosphotyrosine-binding domain — were fused to the death effector domain of FADD. When the construct was transformed into fibroblasts, the synthetic adaptors re-routed the signals that normally lead to growth so that they instead resulted in cell death. Here, the synthetic goal confirmed the power (and, to some extent, the underlying correctness) of a modular model of regulation by this system.

It is clear that this type of restructuring of existing regulatory components will be used in the future to rewire signalling more generally. Here, the analogy with the construction of electrical circuitry has been used by Hasty et al.⁸¹, who recently reviewed some of the spectacular accomplishments in this area (summarized in Box 2).

Synthetic biological 'toys' can also be created. For example, an artificial oscillatory network (a 'repressilator') was constructed in E. coli by Elowitz and Leibler¹⁶(Fig. 5) These synthetic biologists placed into an E. coli host three transcriptional repressor systems that are not together part of any natural biological system, and coupled these to the synthesis of green fluorescent protein. The fluorescent output of the cell oscillated as a function of time, providing a visual signal of the state of the oscillator in the cell. The oscillation period of hours was longer than the time typical to complete a cycle of cell division. This indicates that the state of the oscillator was transmitted from generation to generation, and became a property of a colony of cells.

a | Schematic showing the regulation pattern that forms the basis of a repressilator. Three gene–promoter pairs are arranged so that the product derived from the expression of the gene following a promoter is a repressor for the next promoter in the cycle. Black connecting lines show that promoter P_LlacO1 controls the transcription of the gene tetR-lite, the tetracycline repressor protein TetR represses P_LtetO1, which is the next promoter in the sequence. P_LtetO1 in turn controls the transcription of cI-lite, and the protein CI represses the promoter P_R. Finally, P_R controls the expression of lacI-lite, and the lactose repressor protein LacI represses P_LlacO1, completing the cycle. The suffix '-lite' refers to the presence of tags that increase the degradation rate of the proteins. b | The luminescence pattern of a reporter plasmid that carries GFP under the transcriptional control of the P_LtetO1 promoter, when the reporter construct is transferred to an Escherichia coli in the presence of the repressilator. As the experimental trace shows, the oscillation of the TetR repressor expressed from the repressilator results in the time dependent oscillation of GFP expression. Bars at the bottom of the diagram show the timing of cell division events. The period of the oscillations is longer than the cell division time, and the cycle of oscillations continues in the subsequent generations. Adapted, with permission, from Nature Ref. 16 © (2000) Macmillan Magazines Ltd.

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The repressilator is, of course, a synthetic equivalent of oscillation systems that are found throughout biology⁸². The goal of producing a synthetic oscillator might therefore lead to a deeper understanding of natural oscillators. For example, the repressilator showed noisy behaviour. This might arise from stochastic fluctuations of its component molecules, which are present in very few copies in individual cells. It might also reflect an interaction between the synthetic parts, or between the synthetic parts and the natural parts of the chemically complex biological host. For this type of network design to lead to an improved understanding of naturally occurring networks, we need to go back to analysis. A detailed analytical study of the synthetic system is needed, just as it was for the synthetic genetic systems or for the synthetic metabolic pathways described above.

Other toy systems have emerged in the past year. Some of these involve biomolecules other than proteins. For example, a molecular automaton that plays tic-tac-toe interactively against a human opponent has been built using deoxyribozymes as the modules⁸³. The system is based on a network of 23 molecular-scale LOGIC GATES and one constitutively active deoxyribozyme. These are arrayed in nine wells (3 x 3), which correspond to the game board. To make a move, the molecular automaton analyzes the input oligonucleotide that is associated with a particular move by the human opponent and indicates a move by fluorescence signalling in a response well.

Where are the hazards of synthetic biology?

A provocative title such as 'synthetic biology' suggests a potential for hazard. Accordingly, the past year has seen a call for an 'Asilomar for synthetic biology'⁸⁴, a reference to a conference in Monterey in 1975 that considered the public hazards of the recombinant DNA technology that supports the synthetic biology discussed above.

Much of what is currently called synthetic biology is congruent with the recombinant DNA technology discussed in Asilomar 30 years ago. This includes bacteria that express heterologous genes, proteins in which amino acids have been replaced, and cells with altered regulatory pathways. Placing a new name on an old technology does not create a new hazard.

Those seeking to create artificial chemical systems to support Darwinian processes are, however, creating something new. We must consider the possibility that these artificial systems might cause damage if, for example, they escape from the laboratory. A general principle in biology is relevant for assessing this potential for hazard. The more different an artificial living system is from natural biological systems, the less likely it is that the artificial system will survive in the natural world. A living organism survives when it has access to the resources that it needs, and is more fit than competing organisms in recovering these. Therefore, a completely synthetic life form that has eight nucleotides (Fig. 1) in its genetic alphabet would find survival very difficult if it were to escape from the laboratory. What would it eat? Where would it get its unnatural nucleosides?

This general principle also applies to less exotic examples of engineered life. The 30 years of experience with genetically altered organisms since Asilomar have indicated that virtually any human-engineered organism is less fit than its natural counterpart in a natural environment. If they survive at all in the environment, they do so either under the nurturing of an attentive human, or by ejecting their engineered features. Therefore, an E. coli engineered to play tic-tac-toe might survive in the human intestine, but would probably do so by jettisoning its game-playing skills.

Losing genetic information is much easier than obtaining new information. By contrast with the power of Darwinian processes implied by the Jurassic Park principle ('life finds a way'), Darwinian processes are highly conservative when it comes to creating new functions. When tackling new problems, Darwinian systems take small steps from what they already have; they are not innovators on a large scale. Extinctions are one consequence of this, occurring when the environmental challenges change too fast for Darwinian processes to keep pace.

This is seen, for example, with natural life. The Ebola virus would spread more rapidly if it became airborne and less virulent, as would anthrax bacteria that were transmissible from an infected human host to an uninfected human. The fact that these features have not emerged in these infectious agents indicates the difficulty that Darwinian evolution has in generating such novel properties in existing organisms. In fact, the most hazardous type of bioengineering is the type that is not engineering at all, but reproduces exactly an already existing virulent agent. The synthesis of smallpox virus⁸⁵ is perhaps the riskiest recent example of synthetic biology.

The discussion so far presumes an absence of malice. Suppose one actually wanted to do damage? Would one genetically engineer E. coli carrying ricin to create a threat? Or place fuel and fertilizer in a rented truck and detonate it outside a Federal Building? We know the answer to this question for one individual; Timothy McVeigh used the latter method to damage the federal building in Oklahoma City a decade ago. We do not know it for all individuals.

At the 2004 International Meeting on Synthetic Biology in Boston, one discussion centered on the 'hacker culture', referring to those who create computer viruses. As is the case whenever resources are diverted from productive to non-productive activity, computer viruses and spam cause human deaths. What if a group of people set out to create an airborne Ebola virus? And what if a synthetic biologist, having set the man-on-the-moon goal of creating such a virus, to learn more about how viruses become airborne, told (through the published literature) the biohacker how to do it?

However, the potential benefits of synthetic biology must be juxtaposed with this hazard. History provides only a partial guide. For example, in 1975, the City of Cambridge banned recombinant DNA research in an effort to manage what it perceived as a danger in this technology. In the same decade, an ill-defined syndrome noted in patients having 'acquired immune deficiency' was emerging around the planet as an important health crisis. Without the technology that had been banned by the City of Cambridge, it would have been difficult to learn what the human immunodeficiency virus was, let alone have compounds in hand today that manage the infection. Today, as SARS, bird influenza, and other infectious disease emerge from animal populations, recombinant DNA technology is what distinguishes our ability to manage this threat today and what was possible a century ago.

Conclusions

This might be the last time that a short review on synthetic biology will attempt to span work that ranges from organic chemistry to intercellular interactions. Even in 2005, much has been done to do justice to the individual topics discussed here. Several of these are mentioned in Box 3.

Truly interchangeable parts have, so far, been obtained only by applying synthetic biology to nucleic acids. Here, the independence approximation seems to be adequate because of the repeating charge on the backbone, which remains constant while the information-containing nucleobases are changed. The repeating charge dominates the physical properties of the molecule overall, allowing the pieces to be replaced independently.

Because of the robustness of the interchangeable parts in expanded genetic information systems, we suspect that an artificial chemical system that supports Darwinian evolution — the bridge between non-life and life⁸⁶ — will first be obtained with these. Here, the man-on-the-moon goal cannot help but deepen our understanding of the relationship between chemistry and life.

To obtain the same with proteins will require the development of basic chemical theory, including a better understanding of the behaviour of water, the dissolution of salts in water, and the packing of organic molecules. A well-targeted set of experiments, coupled with the appropriate theory, would help this system develop more rapidly. As with the synthetic biology of nucleic acids, chemistry will drive the development of the field.

Folded protein modules behave with sufficient independence to be useful building modules in synthetic biology. Here, we expect a substantial amount of exciting work over the next few years, as synthetic biologists struggle with the chemical reality, determine which modules behave independently, and define synthetic goals accordingly. Here, synthesis will demonstrate its power as a complement to analysis in the development of theory and the modification of paradigms associated with genetic regulation. The setting of ambitious synthetic goals cannot help but deepen our understanding of the intimate relationship between chemistry and life at the regulatory level, and better understand the emergent properties of complex biological systems.

Box 2 | Engineering regulatory circuits

The engineering of molecular circuits has recently been reviewed by Hasty et al.⁸¹; this article should be consulted for more details of the cases briefly reviewed below, and for further examples.

In one experiment in yeast, Lim and his co-workers rewired Mapk signalling⁹³ and an actin regulatory switch known as N-WASP ^94,95. N-WASP carries an output region that (in isolation) stimulates the polymerization of actin by binding the actin-related protein (Arp) 2/3 complex (see part a of the figure). This activity is autoinhibited, however, by means of two modules from N-WASP, a highly basic (B) motif and a guanosine 5'- triphosphatase (GTPase)-binding domain (GBD). These bind to two activating inputs, the phosphoinositide Pip2 and the activated GTPase Cdc42, where the respective binding disrupts autoinhibition. Because the two activating inputs function cooperatively, N-WASP behaves as an 'AND' gate; the output is positive (actin is polymerized) only if both Pip2 and Cdc42 inputs are present.

Lim and co-workers then attempted to reprogram the input control of N-WASP. They tethered an unrelated modular domain–ligand pair (a PDZ domain and its cognate C-terminal peptide ligand) to the end of the N-WASP output domain (see part b of figure). They expected this to create an unnatural autoinhibitory interaction that could be relieved by the competitive binding of an external PDZ ligand. Under basal conditions, this synthetic switch was not activating. The unnatural autoinhibitory interaction was then removed by adding the PDZ ligand. The maximal activity was close to that of the isolated output domain. The result was the same switch, but one that was turned on by a different activator.

The synthetic biologist then attempted to construct AND gates by tethering two unnatural modular domain-ligand pairs to the N-WASP output domain, replacing the two natural modules (B and GBD). A total of 34 constructs were synthesized and examined for their gating behaviour.

As expected for any real chemical system, the output depended on the concentrations of the input molecules, and was not predictable in an engineering sense. Some switches showed little basal repression. Others could not be activated. A few showed antagonistic gating, with one input activating and the other repressing. A few showed 'OR' gating, where one or the other input generated a positive output.

Nevertheless, about half of the synthetic constructs showed positive AND gating, where both inputs were required to generate a positive output. This input-output relationship was analogous to that seen with native N-WASP, but was obtained from a synthetic system, by using unnatural activators. Figure modified, with permission, from Ref. 95 © (2004) Elsevier Science.