Bisaryl hydrazones as exchangeable biocompatible linkers - Wikidata - wikimedia - TriplyDB

Bisaryl hydrazones as exchangeable biocompatible linkers

Bisaryl hydrazones as exchangeable biocompatible linkers

http://www.wikidata.org/entity/Q41934983

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Site-specific protein modification using lipoic acid ligase and bis-aryl hydrazone formation Enzymatic labeling of proteins: techniques and approaches Dynamic covalent chemistry: Catalysing dynamic libraries.Chemoenzymatic site-specific reversible immobilization and labeling of proteins from crude cellular extract without prior purification using oxime and hydrazine ligation Solid phase extraction of N-linked glycopeptides using hydrazide tip From static to dynamic: escaping kinetic traps in hydrazone-based dynamic combinatorial libraries.Proteomic analysis of fatty-acylated proteins in mammalian cells with chemical reporters reveals S-acylation of histone H3 variants A highly efficient catalyst for oxime ligation and hydrazone-oxime exchange suitable for bioconjugation.Synthesis of an enlarged library of dynamic DNA activators with oxime, disulfide and hydrazone bridges.Dynamic combinatorial/covalent chemistry: a tool to read, generate and modulate the bioactivity of compounds and compound mixtures.New organocatalyst scaffolds with high activity in promoting hydrazone and oxime formation at neutral pH.Aromatic aldehyde and hydrazine activated peptide coated quantum dots for easy bioconjugation and live cell imaging Cyclic acetals as cleavable linkers for affinity capture.Adaptable hydrogel networks with reversible linkages for tissue engineering.Fluorescence quenchers for hydrazone and oxime orthogonal bioconjugation.Chemoenzymatic reversible immobilization and labeling of proteins without prior purification.Water-soluble organocatalysts for hydrazone and oxime formation Development of viral nanoparticles for efficient intracellular delivery.Catch-and-release probes applied to semi-intact cells reveal ubiquitin-specific protease expression in Chlamydia trachomatis infection.Activity-based probes for the study of proteases: recent advances and developments.Rapid covalent ligation of fluorescent peptides to water solubilized quantum dots.Traceless Cleavage of Protein-Biotin Conjugates under Biologically Compatible Conditions.Biophysically defined and cytocompatible covalently adaptable networks as viscoelastic 3D cell culture systems.Invention of stimulus-responsive peptide-bond-cleaving residue (Spr) and its application to chemical biology tools.4-aminophenylalanine as a biocompatible nucleophilic catalyst for hydrazone ligations at low temperature and neutral pH.A cleavable linker based on the levulinoyl ester for activity-based protein profiling.Design and synthesis of a new class of membrane-permeable triazaborolopyridinium fluorescent probes.Highly parallel oligonucleotide purification and functionalization using reversible chemistry.Bromopyridazinedione-mediated protein and peptide bioconjugation.Tunable reagents for multi-functional bioconjugation: reversible or permanent chemical modification of proteins and peptides by control of maleimide hydrolysis.Comparative analysis of cleavable azobenzene-based affinity tags for bioorthogonal chemical proteomics.A simple and effective cleavable linker for chemical proteomics applications Reversible protein affinity-labelling using bromomaleimide-based reagents.Cleavable trifunctional biotin reagents for protein labelling, capture and release.β-D-glucosidase assisted gold dissolution as non-optical and quantifiable detection technique for immunoassays.Dipolar Photosystems: Engineering Oriented Push-Pull Components into Double- and Triple-Channel Surface Architectures.Cleavable Linkers in Chemical Proteomics Applications.Fast and catalyst-free hydrazone ligation via ortho-halo-substituted benzaldehydes for protein C-terminal labeling at neutral pH.Selective transamidation of 3-oxo-N-acyl homoserine lactones by hydrazine derivatives.A Protocol for Protein Profiling Using Chemoselective Cleavable Linker Probes in Semi-permeabilized Cells.

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P2860

Bisaryl hydrazones as exchangeable biocompatible linkers

http://www.wikidata.org/entity/Q41934983

description

2010 nî lūn-bûn

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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

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

2010年论文

@zh

2010年论文

@zh-cn

name

Bisaryl hydrazones as exchangeable biocompatible linkers

@en

type

label

Bisaryl hydrazones as exchangeable biocompatible linkers

@en

prefLabel

Bisaryl hydrazones as exchangeable biocompatible linkers

@en

P1433

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Angewandte Chemie International Edition

P1476

Bisaryl hydrazones as exchangeable biocompatible linkers

@en

P2093

Anouk Dirksen

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

Philip E Dawson

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

Subramanian Yegneswaran

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

P2860

Reversibility of biotin-binding by selective modification of tyrosine in avidin

A monovalent streptavidin with a single femtomolar biotin binding site

Hydrolytic stability of hydrazones and oximes

Nucleophilic catalysis of oxime ligation

Advances in Bioconjugation

Introducing genetically encoded aldehydes into proteins

One-pot and sequential organic chemistry on an enzyme surface to tether a fluorescent probe at the proximity of the active site with restoring enzyme activity.

Engineering soluble monomeric streptavidin with reversible biotin binding capability.

Protein S stimulates inhibition of the tissue factor pathway by tissue factor pathway inhibitor.

Plasma protein S contains zinc essential for efficient activated protein C-independent anticoagulant activity and binding to factor Xa, but not for efficient binding to tissue factor pathway inhibitor.

P304

2023-2027

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

P31

scholarly article

P356

10.1002/ANIE.200906756

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

P407

P433

11

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

P478

49

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

P577

2010-03-01T00:00:00Z

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P698

20183838

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P932

4383167

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