Literature DB >> 26613796

A cleavable biotin tagging reagent that enables the enrichment and identification of carbonylation sites in proteins.

Chelsea M Coffey1, Scott Gronert2.   

Abstract

The utility of a new, cleavable tag for identifying and enriching protein carbonyls is examined. Using a model system, human serum albumin modified with acrolein, the EZ-Link alkoxyamine-PEG4-SS-PEG4-biotin affinity tag, was tested for its ability to label protein carbonyls in proteomic analyses of protein carbonylation. The efficiency of the labeling was assayed and compared to standard biotin hydrazide reagents. The label was also tested in liquid chromatography-tandem mass spectrometry (LC/MS/MS) experiments. The quality of the fragmentation spectra was assessed and the relative detection efficiency of various modification sites was compared to standard biotin hydrazide reagents. Finally, the viability of using the label with streptavidin bead enrichment protocols in a standard proteomics workflow was probed.

Entities:  

Keywords:  Acrolein; Mass spectrometry; Oxidative stress; Protein carbonylation; Proteomics

Mesh:

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Year:  2015        PMID: 26613796     DOI: 10.1007/s00216-015-9176-2

Source DB:  PubMed          Journal:  Anal Bioanal Chem        ISSN: 1618-2642            Impact factor:   4.142


  2 in total

1.  Lipid peroxidation derived reactive carbonyl species in free and conjugated forms as an index of lipid peroxidation: limits and perspectives.

Authors:  Alessandra Altomare; Giovanna Baron; Erica Gianazza; Cristina Banfi; Marina Carini; Giancarlo Aldini
Journal:  Redox Biol       Date:  2021-02-17       Impact factor: 11.799

2.  Chemoproteomic profiling of targets of lipid-derived electrophiles by bioorthogonal aminooxy probe.

Authors:  Ying Chen; Yan Cong; Baiyi Quan; Tong Lan; Xiaoyu Chu; Zi Ye; Xiaomeng Hou; Chu Wang
Journal:  Redox Biol       Date:  2017-04-05       Impact factor: 11.799

  2 in total

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