Nothing Special   »   [go: up one dir, main page]

Satake et al., 2008 - Google Patents

Transmembrane nanopores from porphyrin supramolecules

Satake et al., 2008

Document ID
5253674875011395268
Author
Satake A
Yamamura M
Oda M
Kobuke Y
Publication year
Publication venue
Journal of the American Chemical Society

External Links

Snippet

A porphyrin-based nanopore was constructed through a bilayer lipid membrane (BLM). The macrocyclic porphyrin (the inner diameter= ca. 2.1 nm) having six carboxylic acid groups directed up and down was synthesized by self-assembly of three trisporphyrins, metathesis …
Continue reading at pubs.acs.org (other versions)

Classifications

    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
    • G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay
    • G01N33/543—Immunoassay; Biospecific binding assay with an insoluble carrier for immobilising immunochemicals

Similar Documents

Publication Publication Date Title
Satake et al. Transmembrane nanopores from porphyrin supramolecules
Sakai et al. Synthetic ion channels
Herce et al. Fundamental molecular mechanism for the cellular uptake of guanidinium-rich molecules
Boccalon et al. Metal–organic transmembrane nanopores
Helsel et al. Highly conducting transmembrane pores formed by aromatic oligoamide macrocycles
Talukdar et al. Synthetic ion channels with rigid-rod π-stack architecture that open in response to charge-transfer complex formation
Gong et al. Self-assembling organic nanotubes with precisely defined, sub-nanometer pores: formation and mass transport characteristics
Kitagishi et al. Supramolecular hemoprotein linear assembly by successive interprotein heme− heme pocket interactions
Jeon et al. Artificial ion channel formed by cucurbit [n] uril derivatives with a carbonyl group fringed portal reminiscent of the selectivity filter of K+ channels
Sanchez-Quesada et al. Cyclic peptides as molecular adapters for a pore-forming protein
Kaucher et al. A unimolecular G-quadruplex that functions as a synthetic transmembrane Na+ transporter
Zhao et al. Conformationally controlled oligocholate membrane transporters: learning through water play
Muraoka et al. Ion permeation by a folded multiblock amphiphilic oligomer achieved by hierarchical construction of self-assembled nanopores
Chi et al. Redox-responsive amphiphilic macromolecular [2] pseudorotaxane constructed from a water-soluble pillar [5] arene and a paraquat-containing homopolymer
Wang et al. Self-assembly of concentric hexagons and hierarchical self-assembly of supramolecular metal–organic nanoribbons at the solid/liquid interface
Wang et al. Rationally designed sensing selectivity and sensitivity of an aerolysin nanopore via site-directed mutagenesis
Fyles How do amphiphiles form ion-conducting channels in membranes? Lessons from linear oligoesters
Zhang et al. Construction of a switchable nanochannel for protein transport via a pillar [5] arene-based host–guest system
Cho et al. Water-templated transmembrane nanopores from shape-persistent oligocholate macrocycles
Devi et al. Pd (II)-mediated assembly of porphyrin channels in bilayer membranes
Sun et al. Honeycomb-patterned films fabricated by self-organization of DNA− surfactant complexes
Jiang et al. Bioinspired artificial nanochannels: construction and application
Han et al. Co-assembly of peptides and carbon nanodots: Sensitive analysis of transglutaminase 2
Martins et al. Photoswitchable calixarene activators for controlled peptide transport across lipid membranes
Mittal et al. Four-component catalytic machinery: reversible three-state control of organocatalysis by walking back and forth on a track