Literature DB >> 21074642

Simple chemical tools to expand the range of proteomics applications.

María Jesús García-Murria1, María Luz Valero, Manuel M Sánchez del Pino.   

Abstract

Proteomics is an expanding technology with potential applications in many research fields. Even though many research groups do not have direct access to its main analytical technique, mass spectrometry, they can interact with proteomics core facilities to incorporate this technology into their projects. Protein identification is the analysis most frequently performed in core facilities and is, probably, the most robust procedure. Here we discuss a few chemical reactions that are easily implemented within the conventional protein identification workflow. Chemical modification of proteins with N-hydroxysuccinimide esters, 4-sulfophenyl isothiocyanate, O-methylisourea or through β-elimination/Michael addition can be easily performed in any laboratory. The reactions are quite specific with almost no side reactions. These chemical tools increase considerably the number of applications and have been applied to characterize protein-protein interactions, to determine the N-terminal residues of proteins, to identify proteins with non-sequenced genomes or to locate phosphorylated and O-glycosylated.
Copyright © 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 21074642     DOI: 10.1016/j.jprot.2010.11.002

Source DB:  PubMed          Journal:  J Proteomics        ISSN: 1874-3919            Impact factor:   4.044


  5 in total

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Authors:  Christopher M Crittenden; W Ryan Parker; Zachary B Jenner; Kerry A Bruns; Lucas D Akin; William M McGee; Eugene Ciccimaro; Jennifer S Brodbelt
Journal:  J Am Soc Mass Spectrom       Date:  2016-02-10       Impact factor: 3.109

2.  Combinatorial Labeling Method for Improving Peptide Fragmentation in Mass Spectrometry.

Authors:  Bhanuramanand Kuchibhotla; Sankara Rao Kola; Jagannadham V Medicherla; Swamy V Cherukuvada; Vishnu M Dhople; Madhusudhana Rao Nalam
Journal:  J Am Soc Mass Spectrom       Date:  2017-03-27       Impact factor: 3.109

3.  β-Glucocerebrosidase Modulators Promote Dimerization of β-Glucocerebrosidase and Reveal an Allosteric Binding Site.

Authors:  Jianbin Zheng; Long Chen; Owen S Skinner; Daniel Ysselstein; Jonathan Remis; Peter Lansbury; Renato Skerlj; Michael Mrosek; Ursula Heunisch; Stephan Krapp; Joel Charrow; Michael Schwake; Neil L Kelleher; Richard B Silverman; Dimitri Krainc
Journal:  J Am Chem Soc       Date:  2018-04-30       Impact factor: 15.419

4.  In-situ formed elastin-based hydrogels enhance wound healing via promoting innate immune cells recruitment and angiogenesis.

Authors:  Duo-Mei Tian; Huan-Huan Wan; Jia-Reng Chen; Yong-Bin Ye; Yong He; Yu Liu; Lu-Yao Tang; Zhong-Yuan He; Kai-Zheng Liu; Chong-Jian Gao; Sheng-Lin Li; Qian Xu; Zheng Yang; Chen Lai; Xiao-Jun Xu; Chang-Shun Ruan; Yun-Sheng Xu; Chao Zhang; Liang Luo; Le-Ping Yan
Journal:  Mater Today Bio       Date:  2022-05-21

5.  Characterization of a novel subgroup of extracellular medium-chain-length polyhydroxyalkanoate depolymerases from actinobacteria.

Authors:  Joana Gangoiti; Marta Santos; María Auxiliadora Prieto; Isabel de la Mata; Juan L Serra; María J Llama
Journal:  Appl Environ Microbiol       Date:  2012-08-03       Impact factor: 4.792

  5 in total

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