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针对电压门控钾通道外部前庭的特异性抗体可阻断电流。

Specific antibodies to the external vestibule of voltage-gated potassium channels block current.

作者信息

Zhou B Y, Ma W, Huang X Y

机构信息

Department of Physiology, Cornell University Medical College, New York 10021, USA.

出版信息

J Gen Physiol. 1998 Apr;111(4):555-63. doi: 10.1085/jgp.111.4.555.

Abstract

Using delayed-rectifier potassium channels as examples, we have designed two specific blockers by generating specific antipeptide antibodies to epitopes in the external vestibules of two channel proteins, Kv1.2 and Kv3.1. These antibodies reduced whole-cell Kv1.2 or Kv3.1 currents in transfected cells and the effect was blocked by the corresponding peptide antigen, but not by control peptides. A control antibody had little effect on Kv1.2 currents and the Kv1.2 blocker antibody had limited effect on other related potassium currents. Furthermore, the Kv1.2 blocking antibody inhibited dendrotoxin binding to Kv1.2 channel proteins in transfected cells. Moreover, using the Kv1.2 blocker antibody, we determined the presence and relative contribution of endogenous Kv1.2 to the overall endogenous K+ currents in NG108 neuronal cells. This guided design of specific channel blockers will facilitate future physiological studies on ion channel functions.

摘要

以延迟整流钾通道为例,我们通过针对两种通道蛋白Kv1.2和Kv3.1外部前庭的表位生成特异性抗肽抗体,设计了两种特异性阻滞剂。这些抗体降低了转染细胞中的全细胞Kv1.2或Kv3.1电流,且该效应被相应的肽抗原阻断,但未被对照肽阻断。一种对照抗体对Kv1.2电流几乎没有影响,而Kv1.2阻滞剂抗体对其他相关钾电流的影响有限。此外,Kv1.2阻断抗体抑制了转染细胞中树突毒素与Kv1.2通道蛋白的结合。此外,使用Kv1.2阻滞剂抗体,我们确定了内源性Kv1.2在NG108神经元细胞总体内源性K+电流中的存在及相对贡献。这种特异性通道阻滞剂的指导性设计将有助于未来对离子通道功能的生理学研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cfb/2217123/c4de23bf34f3/JGP7611.f1ab.jpg

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