Cargando…
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...
Autores principales: | , , , , , , , , |
---|---|
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 |
_version_ | 1782152814138490880 |
---|---|
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. |
format | Text |
id | pubmed-2335157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT tianxinsheng molecularcloningexpressionpurificationandcrystallographicanalysisofprrsv3clprotease AT fengyoujun molecularcloningexpressionpurificationandcrystallographicanalysisofprrsv3clprotease AT zhaotiezhu molecularcloningexpressionpurificationandcrystallographicanalysisofprrsv3clprotease AT penghao molecularcloningexpressionpurificationandcrystallographicanalysisofprrsv3clprotease AT yanjinghua molecularcloningexpressionpurificationandcrystallographicanalysisofprrsv3clprotease AT qijianxun molecularcloningexpressionpurificationandcrystallographicanalysisofprrsv3clprotease AT jiangfan molecularcloningexpressionpurificationandcrystallographicanalysisofprrsv3clprotease AT tiankegong molecularcloningexpressionpurificationandcrystallographicanalysisofprrsv3clprotease AT gaofeng molecularcloningexpressionpurificationandcrystallographicanalysisofprrsv3clprotease |