Recombinant expression of novel protegrin-1 dimer and LL-37-linker- histatin-5 hybrid peptide mediated biotin carboxyl carrier protein fusion partner

Antimicrobial peptides (AMPs) hold great promise as potential therapeutic approach for curing of infectious diseases. Prokaryotic protein expression renders high scalability with an effective purification of several heterogeneous proteins. However, it might be inappropriate for recombinant AMPs expr...

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Main Authors: Santhasiri Orrapin, Sorasak Intorasoot
Format: Journal
Published: 2018
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84887833789&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/45415
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-454152018-01-24T06:10:07Z Recombinant expression of novel protegrin-1 dimer and LL-37-linker- histatin-5 hybrid peptide mediated biotin carboxyl carrier protein fusion partner Santhasiri Orrapin Sorasak Intorasoot Antimicrobial peptides (AMPs) hold great promise as potential therapeutic approach for curing of infectious diseases. Prokaryotic protein expression renders high scalability with an effective purification of several heterogeneous proteins. However, it might be inappropriate for recombinant AMPs expression thereby its antimicrobial activity against the host cells. Several fusion partners demonstrated antimicrobial activity neutralization of AMPs expression and purification in Escherichia coli. In order to improve the antimicrobial effect, several hybrid AMPs have been designed and developed. As expected to increase the antimicrobial activity, a dimeric form of porcine protegrin-1 (PG-1) and human LL-37-linker-histatin-5 (LL-37-linker-Hst-5) hybrid peptide were alternatively constructed in this study. Hydroxylamine hydrochloride and thrombin cleavage sites were designed for releasing of hybrid peptide and PG-1 dimer from biotin carboxyl carrier protein (BCCP) fusion partner. The full-length AMPs gene was connected down-stream of BCCP gene using the overlap extension-PCR, cloned into pET-28a vector and expressed in E. coli BL21(DE3)pLysS. After IPTG induction, approximately 20% of BCCP-AMPs was expressed as intracytoplasmic inclusion bodies with an expected molecular weight of 24.5 kDa. The mean of purified and refolded BCCP-AMPs was 1.5 mg/L with 76% purity. The presence of expressed protein was subsequently determined by Western blotting analysis. Finally, radial diffusion assay supported that these peptides displayed functional antimicrobial activity against E. coli and Staphylococcus aureus standard strains. Two novel AMPs established in this study would be potentially developed as extensive intervention for treating of infectious diseases. © 2013 Published by Elsevier Inc. All rights reserved. 2018-01-24T06:10:07Z 2018-01-24T06:10:07Z 2014-01-01 Journal 10465928 2-s2.0-84887833789 10.1016/j.pep.2013.10.010 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84887833789&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/45415
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
description Antimicrobial peptides (AMPs) hold great promise as potential therapeutic approach for curing of infectious diseases. Prokaryotic protein expression renders high scalability with an effective purification of several heterogeneous proteins. However, it might be inappropriate for recombinant AMPs expression thereby its antimicrobial activity against the host cells. Several fusion partners demonstrated antimicrobial activity neutralization of AMPs expression and purification in Escherichia coli. In order to improve the antimicrobial effect, several hybrid AMPs have been designed and developed. As expected to increase the antimicrobial activity, a dimeric form of porcine protegrin-1 (PG-1) and human LL-37-linker-histatin-5 (LL-37-linker-Hst-5) hybrid peptide were alternatively constructed in this study. Hydroxylamine hydrochloride and thrombin cleavage sites were designed for releasing of hybrid peptide and PG-1 dimer from biotin carboxyl carrier protein (BCCP) fusion partner. The full-length AMPs gene was connected down-stream of BCCP gene using the overlap extension-PCR, cloned into pET-28a vector and expressed in E. coli BL21(DE3)pLysS. After IPTG induction, approximately 20% of BCCP-AMPs was expressed as intracytoplasmic inclusion bodies with an expected molecular weight of 24.5 kDa. The mean of purified and refolded BCCP-AMPs was 1.5 mg/L with 76% purity. The presence of expressed protein was subsequently determined by Western blotting analysis. Finally, radial diffusion assay supported that these peptides displayed functional antimicrobial activity against E. coli and Staphylococcus aureus standard strains. Two novel AMPs established in this study would be potentially developed as extensive intervention for treating of infectious diseases. © 2013 Published by Elsevier Inc. All rights reserved.
format Journal
author Santhasiri Orrapin
Sorasak Intorasoot
spellingShingle Santhasiri Orrapin
Sorasak Intorasoot
Recombinant expression of novel protegrin-1 dimer and LL-37-linker- histatin-5 hybrid peptide mediated biotin carboxyl carrier protein fusion partner
author_facet Santhasiri Orrapin
Sorasak Intorasoot
author_sort Santhasiri Orrapin
title Recombinant expression of novel protegrin-1 dimer and LL-37-linker- histatin-5 hybrid peptide mediated biotin carboxyl carrier protein fusion partner
title_short Recombinant expression of novel protegrin-1 dimer and LL-37-linker- histatin-5 hybrid peptide mediated biotin carboxyl carrier protein fusion partner
title_full Recombinant expression of novel protegrin-1 dimer and LL-37-linker- histatin-5 hybrid peptide mediated biotin carboxyl carrier protein fusion partner
title_fullStr Recombinant expression of novel protegrin-1 dimer and LL-37-linker- histatin-5 hybrid peptide mediated biotin carboxyl carrier protein fusion partner
title_full_unstemmed Recombinant expression of novel protegrin-1 dimer and LL-37-linker- histatin-5 hybrid peptide mediated biotin carboxyl carrier protein fusion partner
title_sort recombinant expression of novel protegrin-1 dimer and ll-37-linker- histatin-5 hybrid peptide mediated biotin carboxyl carrier protein fusion partner
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84887833789&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/45415
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