Kelman Z, Yao N, O'Donnell M
Microbiology Department Hearst Research Foundation, Cornell University Medical College, New York, NY 10021, USA.
Gene. 1995 Dec 1;166(1):177-8. doi: 10.1016/0378-1119(95)00556-7.
Escherichia coli expression vectors, based on the pET system, were constructed to allow fusion of a protein kinase (PK) recognition motif, a hemagglutinin (HG) epitope-tag and a His6-tag at the N-terminal portion of a protein of interest. The fusion proteins, that result from expression using these vectors, can be phosphorylated in vitro using cAMP-dependent PK, immunoprecipitated using monoclonal antibody against the HG-epitope, and can be rapidly purified using a Ni2+ column.