IN SILICO ANALYSIS OF INHIBITOR AND SUBSTRATE BINDING SITE OF SERRAPEPTIDASE FROM SERRATIA MARCESCENS MTCC 8708

Authors

  • N. S. Kaviyarasi
  • C. N. Prashantha
  • V. V.s. Suryanarayana Indian Veterinary Research Institute, Hebbal, Bangalore 560024, India

Keywords:

Keywords, Serrapeptidase, anti-inflammation, arthritis, molecular docking, drug discovery, protein-peptide interaction, Bradykinin, Substance-P

Abstract

Objective: Serrapeptidase is a therapeutic enzyme broadly used as an anti-inflammatory drug to treat inflammatory diseases like arthritis, bronchitis, fibrocystic breast disease and sinusitis. The objective of present study is in silco analyzes of the substrate and inhibitor binding sites of serratiopeptidase, expressed from a cloned gene.

Methods: The gene encoding Serrapeptidase was amplified from genomic DNA of Serratia marcescens MTCC 8707, an isolated from the flowers of summer squash plants. The gene was sequenced, the nucleotide sequence of 1464 nucleotides was submitted to Gen Bank nucleotide database and accession number GI: KP869847 obtained. The develop amino acid sequence was used to predict 3D structure using different bioinformatics tools and software's Further, CABS-dock and Swiss Dock, the docking servers were used for enzyme-substrate/inhibitor binding site analysis. The inflammatory mediators, bradykinin, and substance-P were used as substrates, whereas, EDTA and Lisinopril were used as an inhibitor for serrapeptidase. UCSF Chimera program was used for interactive visualization and analysis of docked results.

Results: The docking studies show substrates bradykinin and substance-P bind near zinc binding site with minimum RMSD value and the inhibitors EDTA and lisinopril showed favorable interaction at zinc binding site of serrapeptidase with minimum free energy.

Conclusion: The result of docking studies confirm that the substrate or inhibitor binds near zinc binding domain (HEXXH.) and the peptide bond of the substrate can be effectively cleaved by serrapeptidase.

Keywords: Serrapeptidase, Anti-inflammation, Arthritis, Molecular docking, Drug discovery, Protein-peptide interaction, Bradykinin, Substance-P

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References

Miyata K, Maejima K, Tomoda K, Isono M. Serratia protease part I, Purification and general properties of the enzyme. Agric Biol Chem 1970;34:310-9.

Miyata K, Tomoda K, Isono M. Serratia protease part II, the substrate specificity of the enzyme. Agric Biol Chem 1970;34:1457-5.

Decedue CJ, Broussard EA, Larsan AD, Braymer HD. Purification and characterization of the extracellular proteinase of Serratia marcescens. Biochim Biophys Acta 1979;569:293–8.

Klein G, Kullich W. Short-term treatment of painful osteoarthritis of the knee with oral enzymes. A randomized, double-blind study versus diclofenac. Clin Drug Invest 2000;19:15-8.

Hanaa HA, Nevein NF, Karima AE, Amal HH. Miracle enzymes serrapeptase and nattokinase mitigate neuroinflammation and apoptosis associated with alzheimer’s disease in an experimental model. World J Pharm Pharm Sci 2014;3:876-15.

www.medindia.net/drug-price/serratiopeptidase-combination. [Last accessed on 10 Dec 2015].

Bennett G, Villa. Nimesulide: an NSAID that preferentially inhibits COX-2, and has various unique pharmacological activities. Expert Opin Pharmacother 2000;1:277-86.

Maeda H, Molla A, Oda T, Katsuki T. Internalization of serratia1 protease into cells as an enzyme-inhibitor complex with ï¡2-macroglobulin and regeneration of protease activity and cytotoxicity. J Biol Chem 1987;23:10946-4.

Miyata K, Tomoda K, Isono M. Serratia protease part II, the substrate specificity of the enzyme. Agric Biol Chem 1970;34:1457-5.

Bersanetti PA, Park HY, Bae KS, Son KH, Shin DH, Hirata IY, et al., Characterization of arazyme, an exocellular metalloprotease isolated from Serratia proteamaculans culture medium. Enzyme Microb Technol 2005;37:574–6.

Kurcinski M, Jamroz M, Blaszczyk M, Kolinski A, Kmiecik S. CABS-dock web server for the flexible docking of peptides to proteins without prior knowledge of the binding site. Nucl Acids Res 2015;43:W419-24.

Grosdidier A, Zoete V, Michielin O. Swiss Dock, a protein-small molecule docking web service based on EADock DSS. Nucl Acids Res 2011;39:W270-7.

Kaviyarasi NS, Swaroop S, Suryanarayana VVS. Characterization of a gene encoding serrapeptidase from Serratia marcescens strain (SRM) MTCC 8708, a plant isolate. Int J Curr Microbiol Appl Sci 2015;4:206-14.

Benkert P, Biasini M, Schwede T. Toward the estimation of the absolute quality of individual protein structure models. Bioinformatics 2011;27:343-7.

Altschul SF, Madden TL, Schaffer AA, Zhang J, Zhang Z, Miller W, et al. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucl Acids Res 1997;25:3389-13.

Remmert M, Biegert A, Hauser A, Soding J. HHblits: lightning-fast iterative protein sequence searching by HMM-HMM alignment. Nat Methods 2012;9:173-2.

Hamada K, Yasuo H, Katsuya Y, Hiramatsu H, Fujiwara T, Katsube Y. Crystal structure of serratia protease, a zinc-dependent proteinase from serratia sp. E-15, containing a ï¢-sheet coil motif at 2.0 oA resolution. J Biochem 1996;119:844-7.

Published

01-04-2016

How to Cite

Kaviyarasi, N. S., C. N. Prashantha, and V. V. Suryanarayana. “IN SILICO ANALYSIS OF INHIBITOR AND SUBSTRATE BINDING SITE OF SERRAPEPTIDASE FROM SERRATIA MARCESCENS MTCC 8708”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 8, no. 4, Apr. 2016, pp. 123-8, https://mail.innovareacademics.in/journals/index.php/ijpps/article/view/10713.

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