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Non-fusion expression in Escherichia coli, purification, and characterization of a novel Ca^2+- and phospho-lipid-binding protein annexin B1
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作者 zhangy guoyj sunsh yanhl hey 《第二军医大学学报》 CAS CSCD 北大核心 2005年第5期543-543,共1页
Annexin B1 is a novel member of the annexin family of Ca^2+- and phospholipid-binding proteins from Cysticercus cellulosae. To obtain high quality annexin B1 for biochemical and biophysical analyses, its cDNA was clon... Annexin B1 is a novel member of the annexin family of Ca^2+- and phospholipid-binding proteins from Cysticercus cellulosae. To obtain high quality annexin B1 for biochemical and biophysical analyses, its cDNA was cloned into the prokaryotic expression vector pJLA503 and the translation initiation codon was immediately under the control of the inducible bacteriophage lambda promoters P(R) and P(L). Alter induction by shifting temperature, large amounts of non-fusion protein were produced in Escherichia coli in a soluble form. The recombinant protein was purified to homogeneity by means of two subsequent ion-exchange chromatographic steps. The final yield was about 25 mg/L bacterial culture. 展开更多
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