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新型软体动物特异性α-芋螺毒素可阻断海兔神经元乙酰胆碱受体。

New mollusc-specific alpha-conotoxins block Aplysia neuronal acetylcholine receptors.

作者信息

Fainzilber M, Hasson A, Oren R, Burlingame A L, Gordon D, Spira M E, Zlotkin E

机构信息

Department of Cell and Animal Biology, Silberman Institute of Life Sciences, Hebrew University of Jerusalem, Israel.

出版信息

Biochemistry. 1994 Aug 16;33(32):9523-9. doi: 10.1021/bi00198a018.

Abstract

Two mollusc-specific neurotoxic peptides from the venom of the molluscivorous snail Conus pennaceus are described. These new toxins block acetylcholine receptors (AChR) of cultured Aplysia neurons. Bath application of 0.5-1 microM toxin induces 5-10-mV membrane depolarization, which recovers to the control level within 1-3 min in the presence of the toxin. This response is blocked by 1 mM hexamethonium. Concomitantly with the transient depolarization, the toxins block approximately 90% of the depolarizing responses evoked by brief iontophoretic application of acetylcholine. The pharmacology and amino acid sequences of the toxins (alpha PnIA, GCCSLPPCAANNPDYC-NH2; alpha PnIB, GCCSLPPCALSNPDYC-NH2) enable their classification as novel alpha-conotoxins. The sequences differ from those of previously described alpha-conotoxins in a number of features, the most striking of which is the presence of a single negatively charged residue in the C-terminal loop. This loop contains a positively charged residue in piscivorous venom alpha-conotoxins. In contrast to other alpha-conotoxins, which are selective for vertebrate skeletal muscle nicotinic ACh receptors, these Conus pennaceus toxins block neuronal ACh receptors in molluscs. As such they are new probes which can be used to define subtypes of ACh receptors, and they should be useful tools in the study of structure-function relationships in ACh receptors.

摘要

本文描述了两种从食螺锥螺(Conus pennaceus)毒液中分离出的、具有软体动物特异性的神经毒性肽。这些新型毒素可阻断培养的海兔神经元的乙酰胆碱受体(AChR)。将0.5 - 1微摩尔的毒素施加于浴液中,可诱导5 - 10毫伏的膜去极化,在毒素存在的情况下,1 - 3分钟内可恢复至对照水平。这种反应可被1毫摩尔的六甲铵阻断。与短暂的去极化同时发生的是,毒素可阻断由短暂离子电渗施加乙酰胆碱所诱发的约90%的去极化反应。这些毒素(αPnIA,GCCSLPPCAANNPDYC - NH2;αPnIB,GCCSLPPCALSNPDYC - NH2)的药理学特性和氨基酸序列使其可被归类为新型α - 芋螺毒素。这些序列在许多特征上与先前描述的α - 芋螺毒素不同,其中最显著的特征是C末端环中存在单个带负电荷的残基。在食鱼性毒液的α - 芋螺毒素中,该环含有一个带正电荷的残基。与其他对脊椎动物骨骼肌烟碱型ACh受体具有选择性的α - 芋螺毒素不同,这些锥螺毒素可阻断软体动物中的神经元ACh受体。因此,它们是可用于定义ACh受体亚型的新型探针,并且在研究ACh受体的结构 - 功能关系中应是有用的工具。

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