Literature DB >> 23198996

The methionine sulfoxide reduction system: selenium utilization and methionine sulfoxide reductase enzymes and their functions.

Hwa-Young Kim1.   

Abstract

SIGNIFICANCE: Selenium is utilized in the methionine sulfoxide reduction system that occurs in most organisms. Methionine sulfoxide reductases (Msrs), MsrA and MsrB, are the enzymes responsible for this system. Msrs repair oxidatively damaged proteins, protect against oxidative stress, and regulate protein function, and have also been implicated in the aging process. Selenoprotein forms of Msrs containing selenocysteine (Sec) at the catalytic site are found in bacteria, algae, and animals. RECENT ADVANCES: A selenoprotein MsrB1 knockout mouse has been developed. Significant progress in the biochemistry of Msrs has been made, which includes findings of a novel reducing system for Msrs and of an interesting reason for the use of Sec in the Msr system. The effects of mammalian MsrBs, including selenoprotein MsrB1 on fruit fly aging, have been investigated. Furthermore, it is evident that Msrs are involved in methionine metabolism and regulation of the trans-sulfuration pathway. CRITICAL ISSUES: This article presents recent progress in the Msr field while focusing on the physiological roles of mammalian Msrs, functions of selenoprotein forms of Msrs, and their biochemistry. FUTURE DIRECTIONS: A deeper understanding of the roles of Msrs in redox signaling, the aging process, and metabolism will be achieved. The identity of selenoproteome of Msrs will be sought along with characterization of the identified selenoprotein forms. Exploring new cellular targets and new functions of Msrs is also warranted.

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Year:  2013        PMID: 23198996      PMCID: PMC3763222          DOI: 10.1089/ars.2012.5081

Source DB:  PubMed          Journal:  Antioxid Redox Signal        ISSN: 1523-0864            Impact factor:   8.401


  122 in total

1.  Insights into the role of the metal binding site in methionine-R-sulfoxide reductases B.

Authors:  Alexandre Olry; Sandrine Boschi-Muller; Hong Yu; Daniel Burnel; Guy Branlant
Journal:  Protein Sci       Date:  2005-11       Impact factor: 6.725

2.  Role of structural and functional elements of mouse methionine-S-sulfoxide reductase in its subcellular distribution.

Authors:  Hwa-Young Kim; Vadim N Gladyshev
Journal:  Biochemistry       Date:  2005-06-07       Impact factor: 3.162

3.  Structure and mechanism of peptide methionine sulfoxide reductase, an "anti-oxidation" enzyme.

Authors:  W T Lowther; N Brot; H Weissbach; B W Matthews
Journal:  Biochemistry       Date:  2000-11-07       Impact factor: 3.162

4.  A sulfenic acid enzyme intermediate is involved in the catalytic mechanism of peptide methionine sulfoxide reductase from Escherichia coli.

Authors:  S Boschi-Muller; S Azza; S Sanglier-Cianferani; F Talfournier; A Van Dorsselear; G Branlant
Journal:  J Biol Chem       Date:  2000-11-17       Impact factor: 5.157

5.  Crystal structure of the Escherichia coli peptide methionine sulphoxide reductase at 1.9 A resolution.

Authors:  F Tête-Favier; D Cobessi; S Boschi-Muller; S Azza; G Branlant; A Aubry
Journal:  Structure       Date:  2000-11-15       Impact factor: 5.006

6.  Structure of the GAF domain, a ubiquitous signaling motif and a new class of cyclic GMP receptor.

Authors:  Y S Ho; L M Burden; J H Hurley
Journal:  EMBO J       Date:  2000-10-16       Impact factor: 11.598

7.  S-adenosylmethionine stabilizes cystathionine beta-synthase and modulates redox capacity.

Authors:  Anna Prudova; Zachary Bauman; Aaron Braun; Victor Vitvitsky; Shelly C Lu; Ruma Banerjee
Journal:  Proc Natl Acad Sci U S A       Date:  2006-04-13       Impact factor: 11.205

8.  The repair enzyme peptide methionine-S-sulfoxide reductase is expressed in human epidermis and upregulated by UVA radiation.

Authors:  Fumihide Ogawa; Christina S Sander; Alfred Hansel; Wolf Oehrl; Hubert Kasperczyk; Peter Elsner; Kazuhiro Shimizu; Stefan H Heinemann; Jens J Thiele
Journal:  J Invest Dermatol       Date:  2006-05       Impact factor: 8.551

9.  Different catalytic mechanisms in mammalian selenocysteine- and cysteine-containing methionine-R-sulfoxide reductases.

Authors:  Hwa-Young Kim; Vadim N Gladyshev
Journal:  PLoS Biol       Date:  2005-11-08       Impact factor: 8.029

10.  Alternative first exon splicing regulates subcellular distribution of methionine sulfoxide reductases.

Authors:  Hwa-Young Kim; Vadim N Gladyshev
Journal:  BMC Mol Biol       Date:  2006-03-16       Impact factor: 2.946

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  28 in total

1.  Methionine sulfoxide reductase B1 deficiency does not increase high-fat diet-induced insulin resistance in mice.

Authors:  Jung-Yoon Heo; Hye-Na Cha; Ki Young Kim; Eujin Lee; Suk-Jeong Kim; Yong-Woon Kim; Jong-Yeon Kim; In-Kyu Lee; Vadim N Gladyshev; Hwa-Young Kim; So-Young Park
Journal:  Free Radic Res       Date:  2016-12-09

Review 2.  Regulated methionine oxidation by monooxygenases.

Authors:  Bruno Manta; Vadim N Gladyshev
Journal:  Free Radic Biol Med       Date:  2017-02-14       Impact factor: 7.376

Review 3.  TrxR1 as a potent regulator of the Nrf2-Keap1 response system.

Authors:  Marcus Cebula; Edward E Schmidt; Elias S J Arnér
Journal:  Antioxid Redox Signal       Date:  2015-06-24       Impact factor: 8.401

4.  Selenoprotein MsrB1 deficiency exacerbates acetaminophen-induced hepatotoxicity via increased oxidative damage.

Authors:  Ki Young Kim; Geun-Hee Kwak; Mahendra Pratap Singh; Vadim N Gladyshev; Hwa-Young Kim
Journal:  Arch Biochem Biophys       Date:  2017-10-03       Impact factor: 4.013

5.  Astragaloside IV rescues MPP+-induced mitochondrial dysfunction through upregulation of methionine sulfoxide reductase A.

Authors:  Yue Liu; Li Chong; Xiaoqing Li; Peng Tang; Peng Liu; Chen Hou; Xin Zhang; Rui Li
Journal:  Exp Ther Med       Date:  2017-07-25       Impact factor: 2.447

6.  Essential role of the C-terminal helical domain in active site formation of selenoprotein MsrA from Clostridium oremlandii.

Authors:  Eun Hye Lee; Kitaik Lee; Kwang Yeon Hwang; Hwa-Young Kim
Journal:  PLoS One       Date:  2015-02-18       Impact factor: 3.240

7.  Arrest defective 1 regulates the oxidative stress response in human cells and mice by acetylating methionine sulfoxide reductase A.

Authors:  S-H Shin; H Yoon; Y-S Chun; H-W Shin; M-N Lee; G T Oh; J-W Park
Journal:  Cell Death Dis       Date:  2014-10-23       Impact factor: 8.469

8.  Indolin-2-one compounds targeting thioredoxin reductase as potential anticancer drug leads.

Authors:  Kamila K Kaminska; Helene C Bertrand; Hisashi Tajima; William C Stafford; Qing Cheng; Wan Chen; Geoffrey Wells; Elias S J Arner; Eng-Hui Chew
Journal:  Oncotarget       Date:  2016-06-28

Review 9.  Ca(2+) signaling in the myocardium by (redox) regulation of PKA/CaMKII.

Authors:  Alex S Johnston; Stephan E Lehnart; Joseph R Burgoyne
Journal:  Front Pharmacol       Date:  2015-08-10       Impact factor: 5.810

10.  PEP-1-MsrA ameliorates inflammation and reduces atherosclerosis in apolipoprotein E deficient mice.

Authors:  Yao Wu; Guanghui Xie; Yanyong Xu; Li Ma; Chuanfeng Tong; Daping Fan; Fen Du; Hong Yu
Journal:  J Transl Med       Date:  2015-09-26       Impact factor: 5.531

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