Aittoniemi Jussi, Fotinou Constantina, Craig Tim J, de Wet Heidi, Proks Peter, Ashcroft Frances M
Department of Physiology, Henry Wellcome Centre for Gene Function, University of Oxford, Parks Road, Oxford, UK.
Philos Trans R Soc Lond B Biol Sci. 2009 Jan 27;364(1514):257-67. doi: 10.1098/rstb.2008.0142.
SUR1 is an ATP-binding cassette (ABC) transporter with a novel function. In contrast to other ABC proteins, it serves as the regulatory subunit of an ion channel. The ATP-sensitive (KATP) channel is an octameric complex of four pore-forming Kir6.2 subunits and four regulatory SUR1 subunits, and it links cell metabolism to electrical activity in many cell types. ATPase activity at the nucleotide-binding domains of SUR results in an increase in KATP channel open probability. Conversely, ATP binding to Kir6.2 closes the channel. Metabolic regulation is achieved by the balance between these two opposing effects. Precisely how SUR1 talks to Kir6.2 remains unclear, but recent studies have identified some residues and domains that are involved in both physical and functional interactions between the two proteins. The importance of these interactions is exemplified by the fact that impaired regulation of Kir6.2 by SUR1 results in human disease, with loss-of-function SUR1 mutations causing congenital hyperinsulinism and gain-of-function SUR1 mutations leading to neonatal diabetes. This paper reviews recent data on the regulation of Kir6.2 by SUR1 and considers the molecular mechanisms by which SUR1 mutations produce disease.
SUR1是一种具有新功能的ATP结合盒(ABC)转运蛋白。与其他ABC蛋白不同,它作为离子通道的调节亚基。ATP敏感性(KATP)通道是由四个形成孔道的Kir6.2亚基和四个调节性SUR1亚基组成的八聚体复合物,它在许多细胞类型中将细胞代谢与电活动联系起来。SUR核苷酸结合结构域的ATP酶活性导致KATP通道开放概率增加。相反,ATP与Kir6.2结合会关闭通道。通过这两种相反作用之间的平衡实现代谢调节。SUR1究竟如何与Kir6.2相互作用仍不清楚,但最近的研究已经确定了一些参与这两种蛋白质之间物理和功能相互作用的残基和结构域。SUR1对Kir6.2调节受损导致人类疾病,功能丧失的SUR1突变导致先天性高胰岛素血症,功能获得性SUR1突变导致新生儿糖尿病,这一事实例证了这些相互作用的重要性。本文综述了关于SUR1对Kir6.2调节的最新数据,并探讨了SUR1突变产生疾病的分子机制。