Baker Tania A, Sauer Robert T
Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Biochim Biophys Acta. 2012 Jan;1823(1):15-28. doi: 10.1016/j.bbamcr.2011.06.007. Epub 2011 Jun 27.
ClpXP is a AAA+ protease that uses the energy of ATP binding and hydrolysis to perform mechanical work during targeted protein degradation within cells. ClpXP consists of hexamers of a AAA+ ATPase (ClpX) and a tetradecameric peptidase (ClpP). Asymmetric ClpX hexamers bind unstructured peptide tags in protein substrates, unfold stable tertiary structure in the substrate, and then translocate the unfolded polypeptide chain into an internal proteolytic compartment in ClpP. Here, we review our present understanding of ClpXP structure and function, as revealed by two decades of biochemical and biophysical studies.
ClpXP是一种AAA+蛋白酶,它利用ATP结合和水解产生的能量在细胞内靶向蛋白质降解过程中执行机械工作。ClpXP由一个AAA+ATP酶(ClpX)的六聚体和一个十四聚体肽酶(ClpP)组成。不对称的ClpX六聚体结合蛋白质底物中的无结构肽标签,展开底物中的稳定三级结构,然后将展开的多肽链转运到ClpP的内部蛋白水解区室中。在这里,我们回顾了二十年来的生化和生物物理研究揭示的我们目前对ClpXP结构和功能的理解。