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A novel 4/6-type alpha-conotoxin ViIA selectively inhibits nAchR α3β2 subtype

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成果类型:
期刊论文
作者:
Li, Liang;Liu, Na;Ding, Rong;Wang, Shuo;Liu, Zhuguo;...
通讯作者:
Dai, Qiuyun
作者机构:
[Li, Liang; Zheng, Xing] Univ South China, Inst Pharm & Pharmacol, Hengyang 421001, Peoples R China.
[Wang, Shuo; Dai, Qiuyun; Liu, Na; Li, Liang; Liu, Zhuguo; Li, Haiying; Ding, Rong] Beijing Inst Biotechnol, Beijing 100071, Peoples R China.
通讯机构:
[Dai, Qiuyun] B
Beijing Inst Biotechnol, Beijing 100071, Peoples R China.
语种:
英文
关键词:
α-conotoxin;ViIA;cloning;synthesis;α3β2 nAChR subtype
期刊:
生物化学与生物物理学报
ISSN:
1672-9145
年:
2015
卷:
47
期:
12
页码:
1023-1028
基金类别:
National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [81173035]; National Basic Research Program of ChinaNational Basic Research Program of China [2010CB529802]; National High Technology and Development Program of ChinaNational High Technology Research and Development Program of China [SS2013AA090204]
机构署名:
本校为第一机构
院系归属:
药学与生物科学学院
摘要:
Conotoxins (CTxs) are typically small peptides composed of 12-50 amino acid residues with 2-5 disulfide bridges. Most of them potently and selectively target a wide variety of ion channels and membrane receptors. They are highly valued as neuropharmacological probes and in pharmaceutical development. In this work, a novel α4/6-CTx named ViIA (RDCCSNPPCAHNNPDC-NH2) was identified from a cDNA library of the venom ducts of Conus virgo (C. virgo). ViIA was then synthesized chemically and its disulfide connectivity was identified as 'C1-C3, C2-C4'....

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