DeLaBarre Byron, Brunger Axel T
Howard Hughes Medical Institute, and Department of Molecular and Cellular Physiology, and Stanford Synchrotron Radiation Laboratory, Stanford University, J.H. Clark Center E300-C, 318 Campus Drive, Stanford, CA 94305-5432, USA.
J Mol Biol. 2005 Mar 25;347(2):437-52. doi: 10.1016/j.jmb.2005.01.060.
The AAA (ATPases associated with a variety of cellular activities) family of proteins bind, hydrolyze, and release ATP to effect conformational changes, assembly, or disassembly upon their binding partners and substrate molecules. One of the members of this family, the hexameric p97/valosin-containing protein p97/VCP, is essential for the dislocation of misfolded membrane proteins from the endoplasmic reticulum. Here, we observe large motions and dynamic changes of p97/VCP as it proceeds through the ATP hydrolysis cycle. The analysis is based on crystal structures of four representative ATP hydrolysis states: APO, AMP-PNP, hydrolysis transition state ADP x AlF3, and ADP bound. Two of the structures presented herein, ADP and AMP-PNP bound, are new structures, and the ADP x AlF3 structure was re-refined to higher resolution. The largest motions occur at two stages during the hydrolysis cycle: after, but not upon, nucleotide binding and then following nucleotide release. The motions occur primarily in the D2 domain, the D1 alpha-helical domain, and the N-terminal domain, relative to the relatively stationary and invariant D1alpha/beta domain. In addition to the motions, we observed a transition from a rigid state to a flexible state upon loss of the gamma-phosphate group, and a further increase in flexibility within the D2 domains upon nucleotide release. The domains within each protomer of the hexameric p97/VCP deviate from strict 6-fold symmetry, with the more flexible ADP state exhibiting greater asymmetry compared to the relatively rigid ADP x AlF3 state, suggesting a mechanism of action in which hydrolysis and conformational changes move about the hexamer in a processive fashion.
与多种细胞活动相关的ATP酶(AAA)家族的蛋白质结合、水解并释放ATP,以在其结合伴侣和底物分子上引起构象变化、组装或拆卸。该家族的成员之一,六聚体p97/含缬酪肽蛋白p97/VCP,对于内质网中错误折叠的膜蛋白的错位至关重要。在这里,我们观察到p97/VCP在ATP水解循环过程中的大幅度运动和动态变化。该分析基于四种代表性ATP水解状态的晶体结构:无核苷酸(APO)、AMP-PNP、水解过渡态ADP·AlF3和结合ADP。本文给出的两种结构,即结合ADP和AMP-PNP的结构,是新结构,并且ADP·AlF3结构被重新精修至更高分辨率。最大的运动发生在水解循环的两个阶段:核苷酸结合之后但不是结合时,以及核苷酸释放之后。这些运动主要发生在D2结构域、D1α-螺旋结构域和N端结构域,相对于相对静止且不变的D1α/β结构域。除了这些运动,我们还观察到在γ-磷酸基团丢失后从刚性状态到柔性状态的转变,以及在核苷酸释放后D2结构域内柔性的进一步增加。六聚体p97/VCP每个原体中的结构域偏离严格的六重对称性,与相对刚性的ADP·AlF3状态相比,更柔性的ADP状态表现出更大的不对称性,这表明了一种作用机制,即水解和构象变化以连续的方式在六聚体中移动。