Yamaguchi H, Okuda M, Mikala G, Fukasawa K, Varadi G
Institute of Molecular Pharmacology, Department of Cell Biology, University of Cincinnati, College of Medicine, 231 Bethesda Avenue, Cincinnati, Ohio, 45267-0828, USA.
Biochem Biophys Res Commun. 2000 Jan 7;267(1):156-63. doi: 10.1006/bbrc.1999.1926.
Expression and membrane localization of an epitope-tagged human Ca(2+) channel alpha(1C) subunit were monitored in Xenopus oocytes by confocal microscopy and electrophysiological recording. When alpha(2)/delta and beta(2a) were separately coexpressed with the alpha(1C) subunit, assessment by confocal microscopy showed an 86 and 225% increase of the channel density, respectively. Simultaneous coexpression of alpha(2)/delta and beta(2a) subunits resulted in a cooperative (470%) increase. Electrophysiological measurements performed in parallel revealed that the current augmentation by the alpha(2)/delta subunit is totally attributable to an increase in channel density, whereas the beta(2a) subunit, in addition to increasing channel density, also facilitates channel opening.
通过共聚焦显微镜和电生理记录监测了表位标记的人Ca(2+)通道α(1C)亚基在非洲爪蟾卵母细胞中的表达和膜定位。当α(2)/δ和β(2a)分别与α(1C)亚基共表达时,共聚焦显微镜评估显示通道密度分别增加了86%和225%。α(2)/δ和β(2a)亚基同时共表达导致协同增加(470%)。同时进行的电生理测量表明,α(2)/δ亚基引起的电流增强完全归因于通道密度的增加,而β(2a)亚基除了增加通道密度外,还促进通道开放。