Literature DB >> 10863536

Reflections on the role of the thiol group in biology.

N Haugaard1.   

Abstract

This essay is concerned with the role of the thiol or sulfhydrvl group in cellular function and metabolism and with the important investigations over many years that have led us to a better understanding of the importance of this molecular moiety that plays such a vital role in biology. The tools for measuring the SH group and for inhibiting or regenerating it will be discussed as will its essential role in the actions of many enzymes. The importance of the thiol group in glycolysis and in energy production by mitochondria will be emphasized. Of special interest at present is the fact that certain low molecular weight SH-containing substances can mimic some of the actions of insulin and may become of benefit in the treatment of diabetes mellitus. Finally, the toxic effects of oxygen on metabolism and function will be discussed with particular reference to the possibility that oxidation of thiol groups may play a role in the manifestations of oxygen toxicity.

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Year:  2000        PMID: 10863536     DOI: 10.1111/j.1749-6632.2000.tb06183.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  9 in total

1.  Regulation of the activity of choline acetyl transferase by lipoic acid.

Authors:  N Haugaard; R M Levin
Journal:  Mol Cell Biochem       Date:  2000-10       Impact factor: 3.396

2.  Activation of choline acetyl transferase by dihydrolipoic acid.

Authors:  Niels Haugaard; Robert M Levin
Journal:  Mol Cell Biochem       Date:  2002-01       Impact factor: 3.396

3.  Thioredoxin-1 improves the immunometabolic phenotype of antitumor T cells.

Authors:  Paramita Chakraborty; Shilpak Chatterjee; Pravin Kesarwani; Krishnamurthy Thyagarajan; Supinya Iamsawat; Annika Dalheim; Hung Nguyen; Shanmugam P Selvam; Patrick Nasarre; Gina Scurti; Gary Hardiman; Nilanjana Maulik; Lauren Ball; Vamsi Gangaraju; Mark P Rubinstein; Nancy Klauber-DeMore; Elizabeth G Hill; Besim Ogretmen; Xue-Zhong Yu; Michael I Nishimura; Shikhar Mehrotra
Journal:  J Biol Chem       Date:  2019-04-10       Impact factor: 5.157

4.  Non-protein thiol imaging and quantification in live cells with a novel benzofurazan sulfide triphenylphosphonium fluorogenic compound.

Authors:  Yang Yang; Xiangming Guan
Journal:  Anal Bioanal Chem       Date:  2017-03-29       Impact factor: 4.142

5.  6-Bromo-7-hydroxy-3-methylcoumarin (mBhc) is an efficient multi-photon labile protecting group for thiol caging and three-dimensional chemical patterning.

Authors:  M Mohsen Mahmoodi; Stephanie A Fisher; Roger Y Tam; Philip C Goff; Reid B Anderson; Jane E Wissinger; David A Blank; Molly S Shoichet; Mark D Distefano
Journal:  Org Biomol Chem       Date:  2016-08-16       Impact factor: 3.876

6.  Methoxy-Substituted Nitrodibenzofuran-Based Protecting Group with an Improved Two-Photon Action Cross-Section for Thiol Protection in Solid Phase Peptide Synthesis.

Authors:  Taysir K Bader; Feng Xu; Michael H Hodny; David A Blank; Mark D Distefano
Journal:  J Org Chem       Date:  2020-01-30       Impact factor: 4.354

7.  Benzofurazan sulfides for thiol imaging and quantification in live cells through fluorescence microscopy.

Authors:  Yinghong Li; Yang Yang; Xiangming Guan
Journal:  Anal Chem       Date:  2012-07-26       Impact factor: 6.986

8.  Determination of low molecular thiols and protein sulfhydryl groups using heterocyclic disulfides.

Authors:  A A Shcherbatykh; M S Chernov'yants; L D Popov
Journal:  Amino Acids       Date:  2022-02-03       Impact factor: 3.520

9.  Rapid and thiol-specific high-throughput assay for simultaneous relative quantification of total thiols, protein thiols, and nonprotein thiols in cells.

Authors:  Yang Yang; Xiangming Guan
Journal:  Anal Chem       Date:  2014-12-11       Impact factor: 6.986

  9 in total

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