Robertson B
Department of Biochemistry, Imperial College, London, UK.
Trends Pharmacol Sci. 1997 Dec;18(12):474-83. doi: 10.1016/s0165-6147(97)01140-1.
The past ten years have provided an embarrassment of riches for those interested in cloned voltage-gated K+ (Kv) channels. Details of their physiology and pharmacology in expression systems, and their precise cellular location abound, making them excellent targets for pharmacologists. However, there is still a considerable and important gap in our knowledge between the behaviour of expressed Kv channels and K+ currents in vivo. In this review Brian Robertson focuses on a few of the recent developments in the field of Kv channels, namely modulation of their behaviour by accessory subunits, their control, and localization of identified Kv subunits.
在过去十年里,对于那些对克隆电压门控钾离子(Kv)通道感兴趣的人来说,研究资料多得令人应接不暇。关于它们在表达系统中的生理学和药理学细节,以及它们精确的细胞定位,有大量的研究成果,这使得它们成为药理学家的理想靶点。然而,在我们的认知中,表达的Kv通道的行为与体内钾离子电流之间仍存在相当大且重要的差距。在这篇综述中,布莱恩·罗伯逊重点介绍了Kv通道领域的一些最新进展,即辅助亚基对其行为的调节、它们的控制以及已确定的Kv亚基的定位。