Reversible protein affinity-labelling using bromomaleimide-based reagents. - Wikidata - wikimedia - TriplyDB

Reversible protein affinity-labelling using bromomaleimide-based reagents.

Reversible protein affinity-labelling using bromomaleimide-based reagents.

http://www.wikidata.org/entity/Q42585959

about

Selective and Reversible Photochemical Derivatization of Cysteine Residues in Peptides and Proteins.Selective chemical protein modification.Traceless Cleavage of Protein-Biotin Conjugates under Biologically Compatible Conditions.Chemical Protein Modification through Cysteine.Controlling topological entanglement in engineered protein hydrogels with a variety of thiol coupling chemistries.A mild synthesis of N-functionalised bromomaleimides, thiomaleimides and bromopyridazinediones.A novel synthetic chemistry approach to linkage-specific ubiquitin conjugation.A platform for efficient, thiol-stable conjugation to albumin's native single accessible cysteine.A mild TCEP-based para-azidobenzyl cleavage strategy to transform reversible cysteine thiol labelling reagents into irreversible conjugates.Comparison of metal free polymer–dye conjugation strategies in protic solvents Aryloxymaleimides for cysteine modification, disulfide bridging and the dual functionalization of disulfide bonds

P2860

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P2860

Reversible protein affinity-labelling using bromomaleimide-based reagents.

http://www.wikidata.org/entity/Q42585959

description

2013 nî lūn-bûn

@nan

2013年の論文

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2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

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2013年論文

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2013年论文

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2013年论文

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2013年论文

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name

Reversible protein affinity-labelling using bromomaleimide-based reagents.

@en

Reversible protein affinity-labelling using bromomaleimide-based reagents.

@nl

type

label

Reversible protein affinity-labelling using bromomaleimide-based reagents.

@en

Reversible protein affinity-labelling using bromomaleimide-based reagents.

@nl

prefLabel

Reversible protein affinity-labelling using bromomaleimide-based reagents.

@en

Reversible protein affinity-labelling using bromomaleimide-based reagents.

@nl

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P1433

Organic and Biomolecular Chemistry

P1476

Reversible protein affinity-labelling using bromomaleimide-based reagents.

@en

P2093

Chris P Ryan

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

James R Baker

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

Mark E B Smith

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

Paul R Moody

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

Rachel E Morgan

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

Ramiz I Nathani

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

Richard J Fitzmaurice

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

Stephen Caddick

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

Vijay Chudasama

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

P2860

Cancer proteomics.

Proteomics to unravel platelet-related diseases and identify novel anti-platelet drugs.

Protein modification, bioconjugation, and disulfide bridging using bromomaleimides.

Degradative covalent reactions important to protein stability.

Bisaryl hydrazones as exchangeable biocompatible linkers

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.

A simple and effective cleavable linker for chemical proteomics applications

A tandem orthogonal proteolysis strategy for high-content chemical proteomics.

Catalysis of imido group hydrolysis in a maleimide conjugate.

P304

2408-2411

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scholarly article

P356

10.1039/C3OB40239H

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15

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11

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2013-03-05T00:00:00Z

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235796941

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23462873

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3763775

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