首页    期刊浏览 2024年12月02日 星期一
登录注册

文章基本信息

  • 标题:Crystal structure of the sodium-potassium pump (Na+,K+-ATPase) with bound potassium and ouabain
  • 本地全文:下载
  • 作者:Haruo Ogawa ; Takehiro Shinoda ; Flemming Cornelius
  • 期刊名称:Proceedings of the National Academy of Sciences
  • 印刷版ISSN:0027-8424
  • 电子版ISSN:1091-6490
  • 出版年度:2009
  • 卷号:106
  • 期号:33
  • 页码:13742-13747
  • DOI:10.1073/pnas.0907054106
  • 语种:English
  • 出版社:The National Academy of Sciences of the United States of America
  • 摘要:The sodium-potassium pump (Na+,K+-ATPase) is responsible for establishing Na+ and K+ concentration gradients across the plasma membrane and therefore plays an essential role in, for instance, generating action potentials. Cardiac glycosides, prescribed for congestive heart failure for more than 2 centuries, are efficient inhibitors of this ATPase. Here we describe a crystal structure of Na+,K+-ATPase with bound ouabain, a representative cardiac glycoside, at 2.8 A resolution in a state analogous to E2{middle dot}2K+{middle dot}Pi. Ouabain is deeply inserted into the transmembrane domain with the lactone ring very close to the bound K+, in marked contrast to previous models. Due to antagonism between ouabain and K+, the structure represents a low-affinity ouabain-bound state. Yet, most of the mutagenesis data obtained with the high-affinity state are readily explained by the present crystal structure, indicating that the binding site for ouabain is essentially the same. According to a homology model for the high affinity state, it is a closure of the binding cavity that confers a high affinity.
  • 关键词:cardiac glycosides ; crystallography
国家哲学社会科学文献中心版权所有