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Cloning, expression and mutational studies of a trypsin inhibitor that retains activity even after cyanogen bromide digestion.

作者信息

Bhattacharjee Nilanjana, Banerjee Sayanika, Dutta Samir K

机构信息

Drug Development Diagnostics & Biotechnology Division, CSIR - Indian Institute of Chemical Biology, 4, Raja S.C. Mullick Road, Kolkata 700032, India; Department of Zoology, New Alipore College, L Block, New Alipore, Kolkata 700053, India.

Drug Development Diagnostics & Biotechnology Division, CSIR - Indian Institute of Chemical Biology, 4, Raja S.C. Mullick Road, Kolkata 700032, India.

出版信息

Protein Expr Purif. 2014 Apr;96:26-31. doi: 10.1016/j.pep.2014.01.013. Epub 2014 Feb 1.

DOI:10.1016/j.pep.2014.01.013
PMID:24492011
Abstract

A winged bean trypsin inhibitor (WbTI-2) of molecular mass ∼20kDa, has been cloned and expressed in Escherichiacoli with full activity like the one from seed protein. It completely inhibits trypsin at an enzyme:inhibitor molar ratio of 1:2. PCR with cDNA and genomic DNA using same primers produced about 550 base pair product, which indicated it to be an intronless gene. Through site-directed mutagenesis, the Arg64 has been confirmed as the P1 residue. For the presence of five methionine residues in WbTI-2, cyanogen bromide (CNBr) digestion was carried out. Out of three fragments the one (about 65% of original size) containing the reactive site loop retained 50% activity.

摘要

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