Molecular bases of cyclodextrin adapter interactions with engineered protein nanopores - Wikidata - awgldk - TriplyDB

Molecular bases of cyclodextrin adapter interactions with engineered protein nanopores

Molecular bases of cyclodextrin adapter interactions with engineered protein nanopores

http://www.wikidata.org/entity/Q27660599

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Obstructing toxin pathways by targeted pore blockage 2-Methyl-2,4-pentanediol induces spontaneous assembly of staphylococcal α-hemolysin into heptameric pore structure Semisynthetic Nanoreactor for Reversible Single-Molecule Covalent Chemistry Engineered transmembrane pores.Functional truncated membrane pores.Weakly stable regions and protein-protein interactions in beta-barrel membrane proteins Engineered oligomerization state of OmpF protein through computational design decouples oligomer dissociation from unfolding.Predicting three-dimensional structures of transmembrane domains of β-barrel membrane proteins.Subunit dimers of alpha-hemolysin expand the engineering toolbox for protein nanopores Channel-forming bacterial toxins in biosensing and macromolecule delivery Single-molecule investigation of G-quadruplex folds of the human telomere sequence in a protein nanocavity.Cyclodextrin complexes of reduced bromonoscapine in guar gum microspheres enhance colonic drug delivery Measuring single-molecule DNA hybridization by active control of DNA in a nanopore.Rectification of the current in alpha-hemolysin pore depends on the cation type: the alkali series probed by MD simulations and experiments Molecular modeling study of chiral separation and recognition mechanism of β-adrenergic antagonists by capillary electrophoresis Crown ether-electrolyte interactions permit nanopore detection of individual DNA abasic sites in single molecules Molecular cycloencapsulation augments solubility and improves therapeutic index of brominated noscapine in prostate cancer cells Interactions of high-affinity cationic blockers with the translocation pores of B. anthracis, C. botulinum, and C. perfringens binary toxins.Semisynthetic protein nanoreactor for single-molecule chemistry A stimuli-responsive nanopore based on a photoresponsive host-guest system.Nucleobase Recognition by Truncated α-Hemolysin Pores.Recent advances in nanopore sequencing.Nanopore-based identification of individual nucleotides for direct RNA sequencing.Residue-specific incorporation of non-canonical amino acids into proteins: recent developments and applications.Selection of herbal therapeutics against deltatoxin mediated Clostridial infections.Nucleobase recognition in ssDNA at the central constriction of the alpha-hemolysin pore.Modulation of the current signatures of DNA abasic site adducts in the α-hemolysin ion channel Electrical Current Signatures of DNA Base Modifications in Single Molecules Immobilized in the α-Hemolysin Ion Channel.Cyclodextrin ion channels.Single-molecule interrogation of a bacterial sugar transporter allows the discovery of an extracellular inhibitor.Rapid determination of sample purity and composition by nanopore stochastic sensing.Β-cyclodextrin encapsulated polyphenols as effective antioxidants.Unpicking the determinants of amide NHO[double bond, length as m-dash]C hydrogen bond strength with diphenylacetylene molecular balances.Antibiotics: blocking bacterial defences.Why does β-cyclodextrin prefer to bind nucleotides with an adenine base rather than other 2'-deoxyribonucleoside 5'-monophosphates?Metal-organic complex-functionalized protein nanopore sensor for aromatic amino acids chiral recognition.Enhancement of levodopa stability when complexed with β-cyclodextrin in transdermal patches.Enhanced translocation of poly(dt)45 through an α-hemolysin nanopore by binding with antibody.

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Molecular bases of cyclodextrin adapter interactions with engineered protein nanopores

http://www.wikidata.org/entity/Q27660599

description

2010 nî lūn-bûn

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2010 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2010 թվականի մայիսին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Molecular bases of cyclodextrin adapter interactions with engineered protein nanopores

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Molecular bases of cyclodextrin adapter interactions with engineered protein nanopores

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Molecular bases of cyclodextrin adapter interactions with engineered protein nanopores

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type

label

Molecular bases of cyclodextrin adapter interactions with engineered protein nanopores

@ast

Molecular bases of cyclodextrin adapter interactions with engineered protein nanopores

@en

Molecular bases of cyclodextrin adapter interactions with engineered protein nanopores

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prefLabel

Molecular bases of cyclodextrin adapter interactions with engineered protein nanopores

@ast

Molecular bases of cyclodextrin adapter interactions with engineered protein nanopores

@en

Molecular bases of cyclodextrin adapter interactions with engineered protein nanopores

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PNAS.0914229107

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Molecular bases of cyclodextrin adapter interactions with engineered protein nanopores

@en

P2093

Arijit Banerjee

http://www.w3.org/2001/XMLSchema#string

Ellina Mikhailova

http://www.w3.org/2001/XMLSchema#string

Li-Qun Gu

http://www.w3.org/2001/XMLSchema#string

Michelle Montoya

http://www.w3.org/2001/XMLSchema#string

Stephen Cheley

http://www.w3.org/2001/XMLSchema#string

Yasuo Nagaoka

http://www.w3.org/2001/XMLSchema#string

P2860

The potential and challenges of nanopore sequencing

Substrate recognition mechanism of alpha-1,6-glucosidic linkage hydrolyzing enzyme, dextran glucosidase from Streptococcus mutans

Structure of staphylococcal alpha-hemolysin, a heptameric transmembrane pore

Expanding the genetic code

Outer membrane protein G: Engineering a quiet pore for biosensing.

Prolonged residence time of a noncovalent molecular adapter, beta-cyclodextrin, within the lumen of mutant alpha-hemolysin pores.

Capture of a single molecule in a nanocavity.

A functional protein pore with a "retro" transmembrane domain.

Engineered protein scaffolds as next-generation antibody therapeutics.

Molecular recognition of saccharides by proteins. Insights on the origin of the carbohydrate-aromatic interactions.

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18

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107

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43183254

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20400691

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2889592

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