Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139;
Annu Rev Biochem. 2011;80:587-612. doi: 10.1146/annurev-biochem-060408-172623.
AAA+ family proteolytic machines (ClpXP, ClpAP, ClpCP, HslUV, Lon, FtsH, PAN/20S, and the 26S proteasome) perform protein quality control and are used in regulatory circuits in all cells. These machines contain a compartmental protease, with active sites sequestered in an interior chamber, and a hexameric ring of AAA+ ATPases. Substrate proteins are tethered to the ring, either directly or via adaptor proteins. An unstructured region of the substrate is engaged in the axial pore of the AAA+ ring, and cycles of ATP binding/hydrolysis drive conformational changes that create pulses of pulling that denature the substrate and translocate the unfolded polypeptide through the pore and into the degradation chamber. Here, we review our current understanding of the molecular mechanisms of substrate recognition, adaptor function, and ATP-fueled unfolding and translocation. The unfolding activities of these and related AAA+ machines can also be used to disassemble or remodel macromolecular complexes and to resolubilize aggregates.
AAA+ 家族蛋白酶体(ClpXP、ClpAP、ClpCP、HslUV、Lon、FtsH、PAN/20S 和 26S 蛋白酶体)可执行蛋白质质量控制,并在所有细胞的调控回路中发挥作用。这些机器包含一个隔室蛋白酶,其活性位点被隔离在一个内部隔室中,以及一个六聚体 AAA+ ATP 酶环。底物蛋白通过直接或通过衔接蛋白与环结合。底物的无规卷曲区域参与 AAA+ 环的轴向孔,ATP 结合/水解的循环驱动构象变化,从而产生拉动脉冲,使底物变性,并将展开的多肽穿过孔并进入降解室。在这里,我们回顾了我们目前对底物识别、衔接蛋白功能以及 ATP 驱动的展开和易位的分子机制的理解。这些和相关的 AAA+ 机器的展开活性也可用于拆卸或重塑大分子复合物,并溶解聚集体。