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Title: Direct determination of the redox status of cysteine residues in proteins in vivo

Abstract

Highlights: • A new DNA-maleimide which is cleaved by UV irradiation, DNA-PCMal, was developed. • DNA-PCMal can be used like DNA-Mal to analyze the redox state of cysteine residues. • It is useful for detecting the thiol redox status of a protein in vivo by Western blotting method. • Thus, DNA-PCMal can be a powerful tool for redox proteomics analysis. - Abstract: The redox states of proteins in cells are key factors in many cellular processes. To determine the redox status of cysteinyl thiol groups in proteins in vivo, we developed a new maleimide reagent, a photocleavable maleimide-conjugated single stranded DNA (DNA-PCMal). The DNA moiety of DNA-PCMal is easily removed by UV-irradiation, allowing DNA-PCMal to be used in Western blotting applications. Thereby the state of thiol groups in intracellular proteins can be directly evaluated. This new maleimide compound can provide information concerning redox proteins in vivo, which is important for our understanding of redox networks in the cell.

Authors:
 [1]; ;  [2];  [1];  [3]
  1. Chemical Resources Laboratory, Tokyo Institute of Technology, Nagatsuta 4259-R1-8, Midori-ku, Yokohama 226-8503 (Japan)
  2. Dojindo Laboratories, 2025-5 Tabaru, Mashiki-machi, Kumamoto 861-2202 (Japan)
  3. (CREST), Japan Science and Technology Agency (JST), Tokyo 102-0075 (Japan)
Publication Date:
OSTI Identifier:
22416883
Resource Type:
Journal Article
Resource Relation:
Journal Name: Biochemical and Biophysical Research Communications; Journal Volume: 456; Journal Issue: 1; Other Information: Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA)
Country of Publication:
United States
Language:
English
Subject:
60 APPLIED LIFE SCIENCES; ANIMAL CELLS; ARABIDOPSIS; BIOTIN; CYSTEINE; DNA; IN VIVO; IRRADIATION; PHOSPHATES; PROTEINS; REAGENTS; REDOX PROCESS; RESIDUES; ULTRAVIOLET RADIATION

Citation Formats

Hara, Satoshi, Tatenaka, Yuki, Ohuchi, Yuya, Hisabori, Toru, E-mail: thisabor@res.titech.ac.jp, and Core Research for Evolutional Science and Technology. Direct determination of the redox status of cysteine residues in proteins in vivo. United States: N. p., 2015. Web. doi:10.1016/J.BBRC.2014.11.082.
Hara, Satoshi, Tatenaka, Yuki, Ohuchi, Yuya, Hisabori, Toru, E-mail: thisabor@res.titech.ac.jp, & Core Research for Evolutional Science and Technology. Direct determination of the redox status of cysteine residues in proteins in vivo. United States. doi:10.1016/J.BBRC.2014.11.082.
Hara, Satoshi, Tatenaka, Yuki, Ohuchi, Yuya, Hisabori, Toru, E-mail: thisabor@res.titech.ac.jp, and Core Research for Evolutional Science and Technology. Fri . "Direct determination of the redox status of cysteine residues in proteins in vivo". United States. doi:10.1016/J.BBRC.2014.11.082.
@article{osti_22416883,
title = {Direct determination of the redox status of cysteine residues in proteins in vivo},
author = {Hara, Satoshi and Tatenaka, Yuki and Ohuchi, Yuya and Hisabori, Toru, E-mail: thisabor@res.titech.ac.jp and Core Research for Evolutional Science and Technology},
abstractNote = {Highlights: • A new DNA-maleimide which is cleaved by UV irradiation, DNA-PCMal, was developed. • DNA-PCMal can be used like DNA-Mal to analyze the redox state of cysteine residues. • It is useful for detecting the thiol redox status of a protein in vivo by Western blotting method. • Thus, DNA-PCMal can be a powerful tool for redox proteomics analysis. - Abstract: The redox states of proteins in cells are key factors in many cellular processes. To determine the redox status of cysteinyl thiol groups in proteins in vivo, we developed a new maleimide reagent, a photocleavable maleimide-conjugated single stranded DNA (DNA-PCMal). The DNA moiety of DNA-PCMal is easily removed by UV-irradiation, allowing DNA-PCMal to be used in Western blotting applications. Thereby the state of thiol groups in intracellular proteins can be directly evaluated. This new maleimide compound can provide information concerning redox proteins in vivo, which is important for our understanding of redox networks in the cell.},
doi = {10.1016/J.BBRC.2014.11.082},
journal = {Biochemical and Biophysical Research Communications},
number = 1,
volume = 456,
place = {United States},
year = {Fri Jan 02 00:00:00 EST 2015},
month = {Fri Jan 02 00:00:00 EST 2015}
}