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无活性的GroEL单体可以被分离出来,并重新组装成含有少量结合肽的功能性十四聚体。

Inactive GroEL monomers can be isolated and reassembled to functional tetradecamers that contain few bound peptides.

作者信息

Ybarra J, Horowitz P M

机构信息

Department of Biochemistry, University of Texas Health Science Center, San Antonio 78284-7760, USA.

出版信息

J Biol Chem. 1995 Sep 29;270(39):22962-7. doi: 10.1074/jbc.270.39.22962.

Abstract

For the first time, it has been shown that GroEL can be converted from tetradecamers (14-mers) to monomers under conditions commonly used for the preparation of this chaperonin. The essential requirements are the simultaneous presence of nucleotides such as MgATP or MgADP and a solid-phase anion-exchange medium. The monomers that are formed are metastable in that they only reassemble to a small degree in the absence of additives. These results are in keeping with previous studies on high pressure dissociation that showed the separated monomers display conformational plasticity and can undergo conformational relaxation when relieved of the constraints of the quaternary structure in the oligomer (Gorovits, B., Raman, C. S., and Horowitz, P. M. (1995) J. Biol. Chem. 270, 2061-2066). The monomers display greatly enhanced hydrophobic exposure to the probe 1,1'-bis(4-anilino)naphthalene-5,5'-disulfonic acid, although they are not active in folding functions, and they are unable to form complexes with partially folded rhodanese. The monomers can be completely reassembled to 14-mers by incubation in 1 M ammonium sulfate. There is no evidence of intermediates in the reassembly process. Compared with the original oligomers, the reassembled 14-mers have (a) very low levels of polypeptide contaminants and tryptophan-like fluorescence, two problems that previously hampered spectroscopic studies of GroEL structure and function; (b) functional properties that are very similar to the original material; (c) considerably decreased hydrophobic exposure in the native state; and (d) a similar triggered exposure of hydrophobic surfaces after treatment with urea or spermidine. This study demonstrates that the quaternary structure of GroEL is more labile than previously thought. These results are consistent with suggestions that nucleotides can loosen subunit interactions and show that changes in quaternary structure can operate under conditions where GroEL function has been demonstrated.

摘要

首次发现,在常用于制备这种伴侣蛋白的条件下,GroEL可从十四聚体(14聚体)转化为单体。基本要求是同时存在核苷酸,如MgATP或MgADP以及固相阴离子交换介质。形成的单体是亚稳态的,因为在没有添加剂的情况下它们只会少量重新组装。这些结果与之前关于高压解离的研究一致,该研究表明分离出的单体表现出构象可塑性,并且在解除寡聚体中四级结构的限制时可发生构象弛豫(Gorovits, B., Raman, C. S., and Horowitz, P. M. (1995) J. Biol. Chem. 270, 2061 - 2066)。单体对探针1,1'-双(4-苯胺基)萘-5,5'-二磺酸的疏水暴露大大增强,尽管它们在折叠功能上无活性,并且无法与部分折叠的硫氰酸酶形成复合物。通过在1 M硫酸铵中孵育,单体可完全重新组装成14聚体。在重新组装过程中没有中间体的证据。与原始寡聚体相比,重新组装的14聚体具有:(a)非常低水平的多肽污染物和类色氨酸荧光,这两个问题以前阻碍了对GroEL结构和功能的光谱研究;(b)与原始材料非常相似的功能特性;(c)天然状态下疏水暴露显著降低;以及(d)用尿素或亚精胺处理后疏水表面类似的触发暴露。这项研究表明GroEL的四级结构比以前认为的更不稳定。这些结果与核苷酸可松弛亚基相互作用的观点一致,并表明四级结构的变化可在已证明GroEL功能的条件下发生。

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