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Isolation, expression and characterization of a novel dual serine protease inhibitor, OH-TCI, from king cobra venom
He YY1,2; Liu SB1,2; Lee WH1,3; Qian JQ1,2,3,4; Zhang Y*1,3; zhangy@mail.kiz.ac.cn
2008
发表期刊PEPTIDES
ISSN0196-9781
卷号29期号:10页码:1692-1699
合作性质其它
摘要Snake venom Kunitz/BPTI members are good tools for understanding of structure-functional relationship between serine proteases and their inhibitors. A novel dual Kunitz/BPTI serine proteinase inhibitor named OH-TCI (trypsin- and chymotrypsin-dual inhibitor from Ophiophagus hannah) was isolated from king cobra venom by three chromatographic steps of gel filtration, trypsin affinity and reverse phase HPLC. OH-TCI is composed of 58 amino acid residues with a molecular mass of 6339 Da. Successful expression of OH-TCI was performed as the maltose-binding fusion protein in E. coli DH5 alpha . Much different from Oh11-1, the purified native and recombinant OH-TCI both had strong inhibitory activities against trypsin and chymotrypsin although the sequence identity (74.1%) between them is very high. The inhibitor constants (K-i) of recombinant OH-TCI were 3.91 x 10(-7) and 8.46 x 10(-8) M for trypsin and chymotrypsin, respectively. To our knowledge, it was the first report of Kunitz/BPTI serine proteinase inhibitor from snake venom that had equivalent trypsin and chymotrypsin inhibitory activities.
关键词Serine Proteinase Inhibitor Trypsin Inhibitor Chymotrypsin Inhibitor Snake Venom Kunitz/bpti Family Polypeptide King Cobra
资助者This work was supported by grants from Chinese National Natural Science Foundation (30630014, 30570359 and 30670412) and grants of ‘‘Key Research Direction-KSCX2-YW-R-088’’, ‘‘Western Light’’ Projects from the Chinese Academy of Sciences. ; This work was supported by grants from Chinese National Natural Science Foundation (30630014, 30570359 and 30670412) and grants of ‘‘Key Research Direction-KSCX2-YW-R-088’’, ‘‘Western Light’’ Projects from the Chinese Academy of Sciences. ; This work was supported by grants from Chinese National Natural Science Foundation (30630014, 30570359 and 30670412) and grants of ‘‘Key Research Direction-KSCX2-YW-R-088’’, ‘‘Western Light’’ Projects from the Chinese Academy of Sciences. ; This work was supported by grants from Chinese National Natural Science Foundation (30630014, 30570359 and 30670412) and grants of ‘‘Key Research Direction-KSCX2-YW-R-088’’, ‘‘Western Light’’ Projects from the Chinese Academy of Sciences.
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语种英语
资助者This work was supported by grants from Chinese National Natural Science Foundation (30630014, 30570359 and 30670412) and grants of ‘‘Key Research Direction-KSCX2-YW-R-088’’, ‘‘Western Light’’ Projects from the Chinese Academy of Sciences. ; This work was supported by grants from Chinese National Natural Science Foundation (30630014, 30570359 and 30670412) and grants of ‘‘Key Research Direction-KSCX2-YW-R-088’’, ‘‘Western Light’’ Projects from the Chinese Academy of Sciences. ; This work was supported by grants from Chinese National Natural Science Foundation (30630014, 30570359 and 30670412) and grants of ‘‘Key Research Direction-KSCX2-YW-R-088’’, ‘‘Western Light’’ Projects from the Chinese Academy of Sciences. ; This work was supported by grants from Chinese National Natural Science Foundation (30630014, 30570359 and 30670412) and grants of ‘‘Key Research Direction-KSCX2-YW-R-088’’, ‘‘Western Light’’ Projects from the Chinese Academy of Sciences.
文献类型期刊论文
条目标识符http://ir.kiz.ac.cn/handle/152453/2709
专题科研部门_生物毒素与人类疾病(张云)
科研部门_动物模型与人类重大疾病机理重点实验室
通讯作者zhangy@mail.kiz.ac.cn
作者单位1.Biotoxin Units, Key Laboratory of Animal Models and Human Disease Mechanisms, Kunming Institute of Zoology, Chinese Academy of Sciences, 32 East Jiao Chang Road, Kunming, Yunnan 650223, China
2.Graduate School of the Chinese Academy of Sciences, Beijing 100039, China
3.Kunming Medical College, Kunming, Yunnan 650032, China
4.Department of Anesthesiology, The First Affiliated Hospital of Kunming Medical College, Kunming, Yunnan 650031, China
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He YY,Liu SB,Lee WH,et al. Isolation, expression and characterization of a novel dual serine protease inhibitor, OH-TCI, from king cobra venom[J]. PEPTIDES,2008,29(10):1692-1699.
APA He YY,Liu SB,Lee WH,Qian JQ,Zhang Y*,&zhangy@mail.kiz.ac.cn.(2008).Isolation, expression and characterization of a novel dual serine protease inhibitor, OH-TCI, from king cobra venom.PEPTIDES,29(10),1692-1699.
MLA He YY,et al."Isolation, expression and characterization of a novel dual serine protease inhibitor, OH-TCI, from king cobra venom".PEPTIDES 29.10(2008):1692-1699.
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