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大肠杆菌ATP依赖性蛋白酶ClpXP和ClpAP之间的酶学及结构相似性。

Enzymatic and structural similarities between the Escherichia coli ATP-dependent proteases, ClpXP and ClpAP.

作者信息

Grimaud R, Kessel M, Beuron F, Steven A C, Maurizi M R

机构信息

Laboratory of Cell Biology, NCI, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

J Biol Chem. 1998 May 15;273(20):12476-81. doi: 10.1074/jbc.273.20.12476.

Abstract

Escherichia coli ClpX, a member of the Clp family of ATPases, has ATP-dependent chaperone activity and is required for specific ATP-dependent proteolytic activities expressed by ClpP. Gel filtration and electron microscopy showed that ClpX subunits (Mr 46, 000) associate to form a six-membered ring (Mr approximately 280, 000) that is stabilized by binding of ATP or nonhydrolyzable analogs of ATP. ClpP, which is composed of two seven-membered rings stacked face-to-face, interacts with the nucleotide-stabilized hexamer of ClpX to form a complex that could be isolated by gel filtration. Electron micrographs of negatively stained ClpXP preparations showed side views of 1:1 and 2:1 ClpXP complexes in which ClpP was flanked on either one or both sides by a ring of ClpX. Thus, as was seen for ClpAP, a symmetry mismatch exists in the bonding interactions between the seven-membered rings of ClpP and the six-membered rings of ClpX. Competition studies showed that ClpA may have a slightly higher affinity (approximately 2-fold) for binding to ClpP. Mixed complexes of ClpA, ClpX, and ClpP with the two ATPases bound simultaneously to opposite faces of a single ClpP molecule were seen by electron microscopy. In the presence of ATP or nonhydrolyzable analogs of ATP, ClpXP had nearly the same activity as ClpAP against oligopeptide substrates (>10,000 min-1/tetradecamer of ClpP). Thus, ClpX and ClpA interactions with ClpP result in structurally analogous complexes and induce similar conformational changes that affect the accessibility and the catalytic efficiency of ClpP active sites.

摘要

大肠杆菌ClpX是Clp家族ATP酶的成员之一,具有ATP依赖性伴侣活性,是ClpP所表达的特定ATP依赖性蛋白水解活性所必需的。凝胶过滤和电子显微镜显示,ClpX亚基(分子量46,000)缔合形成一个六聚体环(分子量约280,000),该环通过ATP或ATP的非水解类似物的结合而稳定。由两个面对面堆叠的七聚体环组成的ClpP与ClpX的核苷酸稳定化六聚体相互作用,形成一个可通过凝胶过滤分离的复合物。负染的ClpXP制剂的电子显微照片显示了1:1和2:1 ClpXP复合物的侧视图,其中ClpP的一侧或两侧由ClpX环侧翼。因此,正如在ClpAP中看到的那样,ClpP的七聚体环与ClpX的六聚体环之间的键合相互作用存在对称性不匹配。竞争研究表明,ClpA与ClpP结合的亲和力可能略高(约2倍)。通过电子显微镜观察到ClpA、ClpX和ClpP的混合复合物,其中两个ATP酶同时结合到单个ClpP分子的相对面上。在ATP或ATP的非水解类似物存在下,ClpXP对寡肽底物的活性与ClpAP几乎相同(>10,000 min-1/ClpP的十四聚体)。因此,ClpX和ClpA与ClpP的相互作用导致结构类似的复合物,并诱导类似的构象变化,从而影响ClpP活性位点的可及性和催化效率。

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