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Molecular cloning, expression, purification and crystallographic analysis of PRRSV 3CL protease

3CL protease, a viral chymotrypsin-like proteolytic enzyme, plays a pivotal role in the transcription and replication machinery of many RNA viruses, including porcine reproductive and respiratory syndrome virus (PRRSV). In this study, the full-length 3CL protease from PRRSV was cloned and overexpres...

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Detalles Bibliográficos
Autores principales: Tian, Xinsheng, Feng, Youjun, Zhao, Tiezhu, Peng, Hao, Yan, Jinghua, Qi, Jianxun, Jiang, Fan, Tian, Kegong, Gao, Feng
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2335157/
https://www.ncbi.nlm.nih.gov/pubmed/17671377
http://dx.doi.org/10.1107/S1744309107033234
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author Tian, Xinsheng
Feng, Youjun
Zhao, Tiezhu
Peng, Hao
Yan, Jinghua
Qi, Jianxun
Jiang, Fan
Tian, Kegong
Gao, Feng
author_facet Tian, Xinsheng
Feng, Youjun
Zhao, Tiezhu
Peng, Hao
Yan, Jinghua
Qi, Jianxun
Jiang, Fan
Tian, Kegong
Gao, Feng
author_sort Tian, Xinsheng
collection PubMed
description 3CL protease, a viral chymotrypsin-like proteolytic enzyme, plays a pivotal role in the transcription and replication machinery of many RNA viruses, including porcine reproductive and respiratory syndrome virus (PRRSV). In this study, the full-length 3CL protease from PRRSV was cloned and overexpressed in Escherichia coli. Crystallization experiments yielded crystals that diffracted to 2.1 Å resolution and belong to space group C2, with unit-cell parameters a = 112.31, b = 48.34, c = 42.88 Å, β = 109.83°. The Matthews coefficient and the solvent content were calculated to be 2.49 Å(3) Da(−1) and 50.61%, respectively, for one molecule in the asymmetric unit.
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spelling pubmed-23351572009-08-01 Molecular cloning, expression, purification and crystallographic analysis of PRRSV 3CL protease Tian, Xinsheng Feng, Youjun Zhao, Tiezhu Peng, Hao Yan, Jinghua Qi, Jianxun Jiang, Fan Tian, Kegong Gao, Feng Acta Crystallogr Sect F Struct Biol Cryst Commun Crystallization Communications 3CL protease, a viral chymotrypsin-like proteolytic enzyme, plays a pivotal role in the transcription and replication machinery of many RNA viruses, including porcine reproductive and respiratory syndrome virus (PRRSV). In this study, the full-length 3CL protease from PRRSV was cloned and overexpressed in Escherichia coli. Crystallization experiments yielded crystals that diffracted to 2.1 Å resolution and belong to space group C2, with unit-cell parameters a = 112.31, b = 48.34, c = 42.88 Å, β = 109.83°. The Matthews coefficient and the solvent content were calculated to be 2.49 Å(3) Da(−1) and 50.61%, respectively, for one molecule in the asymmetric unit. International Union of Crystallography 2007-07-28 /pmc/articles/PMC2335157/ /pubmed/17671377 http://dx.doi.org/10.1107/S1744309107033234 Text en © International Union of Crystallography 2007
spellingShingle Crystallization Communications
Tian, Xinsheng
Feng, Youjun
Zhao, Tiezhu
Peng, Hao
Yan, Jinghua
Qi, Jianxun
Jiang, Fan
Tian, Kegong
Gao, Feng
Molecular cloning, expression, purification and crystallographic analysis of PRRSV 3CL protease
title Molecular cloning, expression, purification and crystallographic analysis of PRRSV 3CL protease
title_full Molecular cloning, expression, purification and crystallographic analysis of PRRSV 3CL protease
title_fullStr Molecular cloning, expression, purification and crystallographic analysis of PRRSV 3CL protease
title_full_unstemmed Molecular cloning, expression, purification and crystallographic analysis of PRRSV 3CL protease
title_short Molecular cloning, expression, purification and crystallographic analysis of PRRSV 3CL protease
title_sort molecular cloning, expression, purification and crystallographic analysis of prrsv 3cl protease
topic Crystallization Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2335157/
https://www.ncbi.nlm.nih.gov/pubmed/17671377
http://dx.doi.org/10.1107/S1744309107033234
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