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1.
Chinese Journal of Biotechnology ; (12): 698-702, 2005.
Article in English | WPRIM (Western Pacific) | ID: wpr-237088

ABSTRACT

The c-Abl nonreceptor tyrosine kinase is activated in the cellular responses to genotoxic, oxidative and other forms of stress. Using tagged forms of c-Abl, the present studies demonstrate that c-Abl forms homodimers in cells. The results show that the c-Abl N-terminal regions interact with the corresponding C-terminal regions of both partners in the dimmer. Specifically, the c-Abl SH3 domain binds to a proline-rich motif at amino acids 958-982 in the c-Abl C-terminal region. Deletion of the proline-rich motif disrupts dimmer formation. These findings provide the first evidence that c-Abl forms homodimers and indicate that homodimerization can contribute to the regulation of c-Abl activity.


Subject(s)
Humans , Protein Multimerization , Proto-Oncogene Proteins c-abl , Genetics , Metabolism , src Homology Domains
2.
Chinese Journal of Biotechnology ; (12): 392-396, 2003.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-259180

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)
Chromatography, Affinity , Chromatography, Ion Exchange , Enzyme-Linked Immunosorbent Assay , Escherichia coli , Genetics , Metabolism , Nucleocapsid Proteins , Genetics , Metabolism , Reverse Transcriptase Polymerase Chain Reaction , Severe acute respiratory syndrome-related coronavirus , Genetics , Metabolism , Viral Structural Proteins , Genetics , Metabolism
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