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预测P型ATP酶中的反向转运

Anticipating antiport in P-type ATPases.

作者信息

Niggli Verena, Sigel Erwin

机构信息

Institute of Pathology, University of Bern, Murtenstrasse 31, Bern, Switzerland.

出版信息

Trends Biochem Sci. 2008 Apr;33(4):156-60. doi: 10.1016/j.tibs.2007.12.005. Epub 2008 Mar 17.

Abstract

Cation-transporting P-type ATPases show a high degree of structural and functional homology. Nevertheless, for many members of this large family, the molecular mechanism of transport is unclear; namely, whether transport is electrogenic or not and if countertransport is involved remains to be established. In a few well-studied cases such as the Na(+)-K(+)-ATPase, plasma membrane Ca(2+) ATPase (PMCA) and sarcoplasmic reticulum Ca(2+) ATPase (SERCA) countertransport has been clearly demonstrated. New data based on the crystal structure of SERCA now strongly indicate that countertransport could be mandatory for all P-type ATPases. This concept should be verified for other known and for all newly characterized P-type ATPases.

摘要

阳离子转运P型ATP酶表现出高度的结构和功能同源性。然而,对于这个大家族的许多成员来说,其转运的分子机制尚不清楚;也就是说,转运是否为电生的以及是否涉及反向转运仍有待确定。在一些研究充分的例子中,如钠钾ATP酶、质膜钙ATP酶(PMCA)和肌浆网钙ATP酶(SERCA),反向转运已得到明确证实。基于SERCA晶体结构的新数据现在有力地表明,反向转运可能是所有P型ATP酶所必需的。这一概念应在其他已知的以及所有新鉴定的P型ATP酶中得到验证。

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