Purification, characterization and primary structure of a chymotrypsin inhibitor from Naja atra venom


Autoria(s): Zhou, XD; Jin, Y; Lua, QM; Lia, DS; Zhu, SW; Wang, WY; Xiong, YL
Data(s)

2004

Resumo

A chymotrypsin inhibitor, designated NA-CI, was isolated from the venom of the Chinese cobra Naja atra by three-step chromatography. It inhibited bovine (x-chymotrypsin with a K-i of 25 nM. The molecular mass of NA-CI was determined to be 6403.8 Da by matrix-assisted laser-desorption ionization time-of-flight (MALDI-TOF) analysis. The complete amino acid sequence was determined after digestion of S-carboxymethylated inhibitor with Staphylococcus aureus V8 protease and porcine trypsin. NA-CI was a single polypeptide chain composed of 57 amino acid residues. The main contact site with the protease (PI) has a Phe, showing the specificity of the inhibitor. NA-CI shared great similarity with the chymotrypsin inhibitor from Naja naja venom (identities = 89.5%) and other snake venom protease inhibitors. (C) 2003 Elsevier Inc. All rights reserved.

Identificador

http://159.226.149.42/handle/152453/5317

http://www.irgrid.ac.cn/handle/1471x/50996

Direitos

Purification, characterization and primary structure of a chymotrypsin inhibitor from Naja atra venom

Fonte

Zhou, XD; Jin, Y; Lua, QM; Lia, DS; Zhu, SW; Wang, WY; Xiong, YL.Purification, characterization and primary structure of a chymotrypsin inhibitor from Naja atra venom,137,219-224 ,(SCI-E ):

Palavras-Chave #Biochemistry & Molecular Biology; Zoology
Tipo

期刊论文