Your browser doesn't support javascript.
loading
Over-expression in Escherichia coli and purification of nucleocaspid and membrane protein of SARS coronavirus / 生物工程学报
Chinese Journal of Biotechnology ; (12): 392-396, 2003.
Article in Zh | WPRIM | ID: wpr-259180
Responsible library: WPRO
ABSTRACT
Genes encoding nucleocaspid (N) and membrane (M) protein of SARS coronavirus were obtained by RT-PCR and were cloned into expression vector pET22b and pBV222. DNA sequencing showed that the genes cloned from a patient in Beijing were identical to the gene sequences from reported Toronto strain. The genes were over-expressed in E. coli either as inclusion body or as soluble form. The recombinant proteins were purified by ion-exchange, or ion-exchange followed by metal chelate affinity chromatography. The recombinant N protein was demonstrated highly antigenic and could be employed as antigen to detect SARS antibodies in ELISA system for SARS diagnosis.
Subject(s)
Full text: 1 Index: WPRIM Main subject: Enzyme-Linked Immunosorbent Assay / Viral Structural Proteins / Chromatography, Affinity / Chromatography, Ion Exchange / Nucleocapsid Proteins / Reverse Transcriptase Polymerase Chain Reaction / Severe acute respiratory syndrome-related coronavirus / Escherichia coli / Genetics / Metabolism Language: Zh Journal: Chinese Journal of Biotechnology Year: 2003 Type: Article
Full text: 1 Index: WPRIM Main subject: Enzyme-Linked Immunosorbent Assay / Viral Structural Proteins / Chromatography, Affinity / Chromatography, Ion Exchange / Nucleocapsid Proteins / Reverse Transcriptase Polymerase Chain Reaction / Severe acute respiratory syndrome-related coronavirus / Escherichia coli / Genetics / Metabolism Language: Zh Journal: Chinese Journal of Biotechnology Year: 2003 Type: Article