Generic placeholder image

Protein & Peptide Letters

Editor-in-Chief

ISSN (Print): 0929-8665
ISSN (Online): 1875-5305

Research Article

Molecular Expression of Bioactive Recombinant Methionine Sulfoxide Reductase A (MsrA)

Author(s): M.S. Indhu, Shruthi Nanjundappa, Ramamoorthy Muttu, Upmanyu Vikramaditya, Manish Mahawar, Mihir Sarkar, Taru Sharma Guttula and Sanjeevkumar Bhure*

Volume 28, Issue 1, 2021

Published on: 25 June, 2020

Page: [11 - 17] Pages: 7

DOI: 10.2174/0929866527666200625201628

Price: $65

Abstract

Background: The increase in reactive oxygen species (ROS) production during cryopreservation of semen, leads to oxidation of biomolecules affecting the functionality of spermatozoa. Methionine residues in proteins are highly prone to oxidation and get converted into methionine sulfoxide (MetO). Methionine sulfoxide reductase A (MsrA) can improve the functionality of spermatozoa by reducing the MetO to methionine restoring the lost functionality of the affected proteins.

Objective: The expression of catalytically active recombinant MsrA (rMsrA).

Methods: The msrA gene was PCR amplified, cloned and sequenced. Further, the recombinant clone was used for protein expression and purification. The protein was getting precipitated during dialysis in Tris-buffer. Hence, the purified rMsrA was dialyzed at 4°C against the Tris-buffer pH 7.5 containing MgCl2, KCl, NaCl, urea and triton X-100. During dialysis, changes of buffer were done at every 12 h interval with stepwise reduction in the concentrations of NaCl, urea and triton X-100. The final dialysis was done with buffer containing 10 mM MgCl2, 30 mM KCl, and 150 mM NaCl, 25 mM Tris–HCl pH 7.5. The activity of the rMsrA was checked spectrophotometrically.

Results: The protein BLAST of buffalo MsrA with bovine sequence showed 14 amino acid mismatches. The rMsrA has been purified under denaturing conditions as it was forming inclusion bodies consistently during protein expression. After renaturation, the purified 33 kDa rMsrA was catalytically active by biochemical assay.

Conclusion: The rMsrA expressed in prokaryotic system is catalytically active and can be used for supplementation to semen extender to repair the oxidatively damaged seminal plasma proteins that occur during cryopreservation.

Keywords: Buffalo, recombinant MsrA, expression, enzyme activity, spectroscopic method, biochemical assay.

Graphical Abstract
[1]
Bandyopadhyay, U.; Das, D.; Banerjee, R.K. Reactive oxygen species: oxidative damage and pathogenesis. Curr. Sci., 1999, 77, 658-666.
[2]
Birben, E.; Sahiner, U.M.; Sackesen, C.; Erzurum, S.; Kalayci, O. Oxidative stress and antioxidant defense. World Allergy Organ. J., 2012, 5(1), 9-19.
[http://dx.doi.org/10.1097/WOX.0b013e3182439613] [PMID: 23268465]
[3]
Hawkins, C.L.; Pattison, D.I.; Davies, M.J. Hypochlorite-induced oxidation of amino acids, peptides and proteins. Amino Acids, 2003, 25(3-4), 259-274.
[http://dx.doi.org/10.1007/s00726-003-0016-x] [PMID: 14661089]
[4]
Moskovitz, J. Methionine sulfoxide reductases: ubiquitous enzymes involved in antioxidant defense, protein regulation, and prevention of aging-associated diseases. Biochim. Biophys. Acta, 2005, 1703(2), 213-219.
[http://dx.doi.org/10.1016/j.bbapap.2004.09.003] [PMID: 15680229]
[5]
Moskovitz, J.; Poston, J.M.; Berlett, B.S.; Nosworthy, N.J.; Szczepanowski, R.; Stadtman, E.R. Identification and characterization of a putative active site for peptide methionine sulfoxide reductase (MsrA) and its substrate stereospecificity. J. Biol. Chem., 2000, 275(19), 14167-14172.
[http://dx.doi.org/10.1074/jbc.275.19.14167] [PMID: 10799493]
[6]
Kim, H-Y.; Gladyshev, V.N. Methionine sulfoxide reduction in mammals: characterization of methionine-R-sulfoxide reductases. Mol. Biol. Cell, 2004, 15(3), 1055-1064.
[http://dx.doi.org/10.1091/mbc.e03-08-0629] [PMID: 14699060]
[7]
Moskovitz, J.; Stadtman, E.R. Selenium-deficient diet enhances protein oxidation and affects methionine sulfoxide reductase (MsrB) protein level in certain mouse tissues. Proc. Natl. Acad. Sci. USA, 2003, 100(13), 7486-7490.
[http://dx.doi.org/10.1073/pnas.1332607100] [PMID: 12792026]
[8]
Moskovitz, J. Prolonged selenium-deficient diet in MsrA knockout mice causes enhanced oxidative modification to proteins and affects the levels of antioxidant enzymes in a tissue-specific manner. Free Radic. Res., 2007, 41(2), 162-171.
[http://dx.doi.org/10.1080/10715760600978823] [PMID: 17364942]
[9]
Levine, R.L.; Berlett, B.S.; Moskovitz, J.; Mosoni, L.; Stadtman, E.R. Methionine residues may protect proteins from critical oxidative damage. Mech. Ageing Dev., 1999, 107(3), 323-332.
[http://dx.doi.org/10.1016/S0047-6374(98)00152-3] [PMID: 10360685]
[10]
Kim, H-Y.; Gladyshev, V.N. Methionine sulfoxide reductases: selenoprotein forms and roles in antioxidant protein repair in mammals. Biochem. J., 2007, 407(3), 321-329.
[http://dx.doi.org/10.1042/BJ20070929] [PMID: 17922679]
[11]
Bailey, J.L.; Bilodeau, J.F.; Cormier, N. Semen cryopreservation in domestic animals: a damaging and capacitating phenomenon. J. Androl., 2000, 21(1), 1-7.
[PMID: 10670514]
[12]
Senatore, E.M.; Verberckmoes, S.; Pascale, M.; Presicce, G.A. A deep utero-tubal semen deposition in Mediterranean Italian buffaloes using a new artificial insemination device. Reprod. Fertil. Dev., 2004, 16, 133.
[http://dx.doi.org/10.1071/RDv16n1Ab21]
[13]
Kumaresan, A.; Ansari, M.R.; Garg, A. Modulation of post-thaw sperm functions with oviductal proteins in buffaloes. Anim. Reprod. Sci., 2005, 90(1-2), 73-84.
[http://dx.doi.org/10.1016/j.anireprosci.2005.01.009] [PMID: 15950408]
[14]
Aitken, R.J.; Roman, S.D. Antioxidant systems and oxidative stress in the testes. Oxid. Med. Cell. Longev., 2008, 1(1), 15-24.
[http://dx.doi.org/10.4161/oxim.1.1.6843] [PMID: 19794904]
[15]
Rahman, M.A.; Nelson, H.; Weissbach, H.; Brot, N. Cloning, sequencing, and expression of the Escherichia coli peptide methionine sulfoxide reductase gene. J. Biol. Chem., 1992, 267(22), 15549-15551.
[PMID: 1386361]
[16]
Moskovitz, J.; Weissbach, H.; Brot, N. Cloning the expression of a mammalian gene involved in the reduction of methionine sulfoxide residues in proteins. Proc. Natl. Acad. Sci. USA, 1996, 93(5), 2095-2099.
[http://dx.doi.org/10.1073/pnas.93.5.2095] [PMID: 8700890]
[17]
Kuschel, L.; Hansel, A.; Schönherr, R.; Weissbach, H.; Brot, N.; Hoshi, T.; Heinemann, S.H. Molecular cloning and functional expression of a human peptide methionine sulfoxide reductase (hMsrA). FEBS Lett., 1999, 456(1), 17-21.
[http://dx.doi.org/10.1016/S0014-5793(99)00917-5] [PMID: 10452521]
[18]
Petropoulos, I.; Mary, J.; Perichon, M.; Friguet, B. Rat peptide methionine sulphoxide reductase: cloning of the cDNA, and down-regulation of gene expression and enzyme activity during aging. Biochem. J., 2001, 355(Pt 3), 819-825.
[http://dx.doi.org/10.1042/bj3550819] [PMID: 11311146]
[19]
Wu, P-F.; Zhang, Z.; Guan, X-L.; Li, Y.L.; Zeng, J.H.; Zhang, J.J.; Long, L.H.; Hu, Z.L.; Wang, F.; Chen, J.G. A specific and rapid colorimetric method to monitor the activity of methionine sulfoxide reductase A. Enzyme Microb. Technol., 2013, 53(6-7), 391-397.
[http://dx.doi.org/10.1016/j.enzmictec.2013.08.005] [PMID: 24315642]
[20]
Petropoulos, I.; Friguet, B. Maintenance of proteins and aging: the role of oxidized protein repair. Free Radic. Res., 2006, 40(12), 1269-1276.
[http://dx.doi.org/10.1080/10715760600917144] [PMID: 17090416]
[21]
Chondrogianni, N.; Petropoulos, I.; Grimm, S.; Georgila, K.; Catalgol, B.; Friguet, B.; Grune, T.; Gonos, E.S. Protein damage, repair and proteolysis. Mol. Aspects Med., 2014, 35, 1-71.
[http://dx.doi.org/10.1016/j.mam.2012.09.001] [PMID: 23107776]
[22]
Picot, C.R.; Petropoulos, I.; Perichon, M.; Moreau, M.; Nizard, C.; Friguet, B. Overexpression of MsrA protects WI-38 SV40 human fibroblasts against H2O2-mediated oxidative stress. Free Radic. Biol. Med., 2005, 39(10), 1332-1341.
[http://dx.doi.org/10.1016/j.freeradbiomed.2005.06.017] [PMID: 16257642]
[23]
Achilli, C.; Ciana, A.; Minetti, G. The discovery of methionine sulfoxide reductase enzymes: an historical account and future perspectives. Biofactors, 2015, 41(3), 135-152.
[http://dx.doi.org/10.1002/biof.1214] [PMID: 25963551]

Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy