Jones Peter M, O'Mara Megan L, George Anthony M
Institute for Biotechnology of Infectious Diseases, Faculty of Science, University of Technology Sydney, P.O. Box 123, Broadway, NSW 2007, Australia.
Trends Biochem Sci. 2009 Oct;34(10):520-31. doi: 10.1016/j.tibs.2009.06.004. Epub 2009 Sep 11.
ATP-binding cassette (ABC) transporters form one of the largest and most ancient of protein families. ABC transporters couple hydrolysis of ATP to vectorial translocation of diverse substrates across cellular membranes. Many human ABC transporters are medically important in causing, for example, multidrug resistance to cytotoxic drugs. Seven complete prokaryotic structures and one eukaryotic structure have been solved for transporters from 2002 to date, and a wealth of research is being conducted on and around these structures to resolve the mechanistic conundrum of how these transporters couple ATP hydrolysis in cytosolic domains to substrate translocation through the transmembrane pore. Many questions remained unanswered about this mechanism, despite a plethora of data and a number of interesting and controversial models.
ATP结合盒(ABC)转运蛋白构成了最大且最古老的蛋白质家族之一。ABC转运蛋白将ATP水解与多种底物跨细胞膜的向量转运偶联起来。许多人类ABC转运蛋白在医学上具有重要意义,例如导致对细胞毒性药物的多药耐药性。从2002年至今,已解析出7种完整的原核生物结构和1种真核生物结构的转运蛋白,并且围绕这些结构正在开展大量研究,以解决这些转运蛋白如何将胞质结构域中的ATP水解与通过跨膜孔的底物转运偶联起来这一机制难题。尽管有大量数据以及许多有趣且有争议的模型,但关于这一机制仍有许多问题未得到解答。