Precursors of three unique cysteine-rich peptides from the scorpion Buthus martensii Karsch

被引:9
|
作者
Zhu, SY [1 ]
Li, WX [1 ]
机构
[1] Wuhan Univ, Coll Life Sci, Dept Biotechnol, Wuhan 430072, Hubei Province, Peoples R China
基金
中国国家自然科学基金;
关键词
bioactive peptides; Buthus martensii Karsch; cystine framework; ion channels; molecular cloning; serine protease inhibitor; scorpion; sequence comparison;
D O I
10.1016/S1096-4959(02)00020-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Scorpion venoms contain a large number of small peptides with diverse primary structures and unique pharmacological functions. From a cDNA library prepared from venom glands of the Chinese scorpion Buthus martensii Karsch, clones encoding precursors of three unique cysteine-rich peptides named BmTXKS3, BmTXLP2 and BmAP1 have been isolated and sequenced. These precursors are composed of 54, 94 and 89 amino acids, respectively. containing a signal peptide in their N-termini. Sequence analysis shows that BmTXKS3 and BmTXLP2 are two novel members of a scorpion toxin family sharing cysteine-stabilized alpha-helical folds. BmAP1 possesses a distinctive cystine framework, which is similar to some serine protease inhibitors and the segments of several extracellular proteins. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:749 / 756
页数:8
相关论文
共 50 条
  • [21] Recombinant Expression, Functional Characterization of Two Scorpion Venom Toxins with Three Disulfide Bridges from the Chinese Scorpion Buthus martensii Karsch
    Lin, Shengguo
    Wang, Xuelin
    Hu, Xueyao
    Zhao, Yongshan
    Zhao, Mingyi
    Zhang, Jinghai
    Cui, Yong
    PROTEIN AND PEPTIDE LETTERS, 2017, 24 (03): : 235 - 240
  • [22] Molecular characterization of a K+ channel blocker in the scorpion Buthus martensii Karsch
    Zhu, SY
    Zeng, XC
    Li, WX
    Jiang, DH
    CHINESE SCIENCE BULLETIN, 2000, 45 (08): : 739 - 743
  • [23] A K~+ channel-blocking peptide from venom of Chinese scorpion Buthus martensii Karsch
    吴宫
    魏东升
    何发虎
    胡国渊
    吴厚铭
    ActaPharmacologicaSinica, 1998, (04) : 22 - 26
  • [24] Crystal structure of an acidic neurotoxin from scorpion Buthus martensii karsch at 1.85 angstrom resolution
    Li, HM
    Wang, DC
    Zeng, ZH
    Jin, L
    Hu, RQ
    JOURNAL OF MOLECULAR BIOLOGY, 1996, 261 (03) : 415 - 431
  • [25] Characterization of novel cysteine-rich antimicrobial peptides from scorpion blood
    EhretSabatier, L
    Loew, D
    Goyffon, M
    Fehlbaum, P
    Hoffmann, JA
    vanDorsselaer, A
    Bulet, P
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (47) : 29537 - 29544
  • [26] cDNA sequences of two anti-mammals neurotoxins from scorpion Buthus martensii Karsch
    Xiong, YM
    Ling, MH
    Zhao, T
    Wang, DC
    Chi, CW
    ACTA BIOCHIMICA ET BIOPHYSICA SINICA, 1997, 29 (02): : 200 - 205
  • [27] Cloning, expression, and pharmacological activity of BmK AS, an active peptide from scorpion Buthus martensii Karsch
    Shao, Jian-Hua
    Wang, Yue-Qiu
    Wu, Xiao-Yan
    Jiang, Rui
    Zhang, Rong
    Wu, Chun-Fu
    Zhang, Jing-Hai
    BIOTECHNOLOGY LETTERS, 2008, 30 (01) : 23 - 29
  • [28] Preliminary crystallographic studies of a neurotoxin with a high toxicity from Chinese scorpion Buthus martensii Karsch
    李宏民
    刘延顺
    金雷
    王淼
    赵彤
    王大成
    Chinese Science Bulletin, 1995, (14) : 1216 - 1219
  • [29] Cloning, expression, and pharmacological activity of BmK AS, an active peptide from scorpion Buthus martensii Karsch
    Jian-Hua Shao
    Yue-Qiu Wang
    Xiao-Yan Wu
    Rui Jiang
    Rong Zhang
    Chun-Fu Wu
    Jing-Hai Zhang
    Biotechnology Letters, 2008, 30 : 23 - 29
  • [30] Scorpion toxins from Buthus martensii Karsch all possess a predicted α-tight-turn
    Hahin R.
    Chen Z.
    Wang D.
    Reddy G.
    Mao L.
    Cell Biochemistry and Biophysics, 2002, 37 (3) : 169 - 186