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钾离子通道单个位点突变对钾离子/铷离子选择性及内部四乙铵阻断的调节作用

Regulation of K+/Rb+ selectivity and internal TEA blockade by mutations at a single site in K+ pores.

作者信息

Taglialatela M, Drewe J A, Kirsch G E, De Biasi M, Hartmann H A, Brown A M

机构信息

Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX 77030.

出版信息

Pflugers Arch. 1993 Apr;423(1-2):104-12. doi: 10.1007/BF00374967.

Abstract

A conservative reversion at position 374 in a chimeric K+ pore, CHM, switched the preferred ionic conductance from K+ to Rb+. To understand how selectivity was switched, codons for 18 different amino acids were substituted at position 374 in each of two different K+ channels CHM and Kv2.1, the host channel for CHM. After injection of cRNA into Xenopus oocytes, less than half of the substituted mutants expressed functional channels. In both CHM and Kv2.1, channels with the substituted hydrophobic residues Val or Ile expressed Rb(+)-preferring pores while channels with the substituted polar residues Thr or Ser expressed K(+)-preferring pores. Val or Ile stabilized while Thr or Ser destabilized blockade by internal tetraethylammonium (TEA) confirming the importance of hydrophobic interactions for blockade. TEA blockade was dependent upon the charge carrier and was more effective in the presence of the ion having the larger conductance. The results are consistent with a model in which the side chains at position 374 form a filter for K+ and Rb+ ions and a site for blockade by internal TEA.

摘要

嵌合钾离子通道CHM中374位的保守性逆转,将优先离子电导从钾离子切换为铷离子。为了解选择性是如何切换的,在两种不同的钾离子通道CHM及其宿主通道Kv2.1的374位上替换了18种不同氨基酸的密码子。将体外转录RNA(cRNA)注入非洲爪蟾卵母细胞后,不到一半的替换突变体表达出功能性通道。在CHM和Kv2.1中,替换为疏水残基缬氨酸(Val)或异亮氨酸(Ile)的通道表现出偏好铷离子的孔道,而替换为极性残基苏氨酸(Thr)或丝氨酸(Ser)的通道表现出偏好钾离子的孔道。缬氨酸或异亮氨酸使内部四乙铵(TEA)的阻断作用稳定,而苏氨酸或丝氨酸则使其不稳定,这证实了疏水相互作用对阻断的重要性。TEA阻断作用取决于电荷载体,并且在存在电导较大的离子时更有效。这些结果与一个模型一致,即374位的侧链形成了钾离子和铷离子的过滤器以及内部TEA的阻断位点。

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