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重建的AAA+马达揭示了由三磷酸腺苷驱动的机器的工作原理。

Rebuilt AAA + motors reveal operating principles for ATP-fuelled machines.

作者信息

Martin Andreas, Baker Tania A, Sauer Robert T

机构信息

Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.

出版信息

Nature. 2005 Oct 20;437(7062):1115-20. doi: 10.1038/nature04031.

Abstract

Hexameric ring-shaped ATPases of the AAA + (for ATPases associated with various cellular activities) superfamily power cellular processes in which macromolecular structures and complexes are dismantled or denatured, but the mechanisms used by these machine-like enzymes are poorly understood. By covalently linking active and inactive subunits of the ATPase ClpX to form hexamers, here we show that diverse geometric arrangements can support the enzymatic unfolding of protein substrates and translocation of the denatured polypeptide into the ClpP peptidase for degradation. These studies indicate that the ClpX power stroke is generated by ATP hydrolysis in a single subunit, rule out concerted and strict sequential ATP hydrolysis models, and provide evidence for a probabilistic sequence of nucleotide hydrolysis. This mechanism would allow any ClpX subunit in contact with a translocating polypeptide to hydrolyse ATP to drive substrate spooling into ClpP, and would prevent stalling if one subunit failed to bind or hydrolyse ATP. Energy-dependent machines with highly diverse quaternary architectures and molecular functions could operate by similar asymmetric mechanisms.

摘要

AAA +(与各种细胞活动相关的ATP酶)超家族的六聚体环状ATP酶为细胞过程提供动力,在这些过程中,大分子结构和复合物被拆解或变性,但这些类似机器的酶所使用的机制却鲜为人知。通过将ATP酶ClpX的活性和非活性亚基共价连接以形成六聚体,我们在此表明,不同的几何排列可以支持蛋白质底物的酶促解折叠以及变性多肽转运到ClpP肽酶中进行降解。这些研究表明,ClpX的动力冲程是由单个亚基中的ATP水解产生的,排除了协同和严格顺序ATP水解模型,并为核苷酸水解的概率序列提供了证据。这种机制将允许任何与转运多肽接触的ClpX亚基水解ATP,以驱动底物卷入ClpP,并在一个亚基未能结合或水解ATP时防止停滞。具有高度多样化四级结构和分子功能的能量依赖型机器可能通过类似的不对称机制运行。

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