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人碳酸酐酶II折叠及其亲环蛋白催化作用的动力学分析

A kinetic analysis of the folding of human carbonic anhydrase II and its catalysis by cyclophilin.

作者信息

Kern G, Kern D, Schmid F X, Fischer G

机构信息

Max-Planck-Arbeitsgruppe Enzymologie der Peptidbindung, Halle/Saale, Germany.

出版信息

J Biol Chem. 1995 Jan 13;270(2):740-5. doi: 10.1074/jbc.270.2.740.

Abstract

The kinetics of unfolding and refolding of human carbonic anhydrase II (HCAII) and its catalysis by the peptidyl-prolyl-cis/trans-isomerase cyclophilin were investigated. HCAII contains 15 trans- and 2 cis-prolyl peptide bonds, and, when long-term denatured, virtually all unfolded molecules contain non-native prolyl isomers. In unfolding these molecules (Us) are produced slowly in a biphasic process reflecting the isomerization of several trans-prolines and of one cis-proline. In refolding, the rapid formation of an intermediate of the molten globule type is followed by several slow prolyl isomerizations, which determine the rate of reactivation. By a short 10-s incubation in 5.0 M guanidinium chloride at 2 degrees C, unfolded HCAII species with all prolines still in the native conformation (Uf) could be produced. Surprisingly, only a fraction of Uf refolds rapidly, but the other molecules refold slowly. Evidently, some prolyl peptide bonds isomerize early in refolding, at the stage of the molten globule and as a consequence, molecules with incorrect prolyl isomers are formed in competition with the productive folding of Uf. This fraction of slow-folding molecules is strongly increased when cyclophilin is present, because it accelerates the formation of non-native prolyl isomers as long as the molecules remain in the molten globule state. Later cyclophilin catalyzes the isomerization of these prolyl peptide bonds toward the native state, which are stabilized in their conformation by further folding to the native state. This catalysis is very efficient, because only prolines that are accessible in the molten globule are involved in this sequence of isomerization and reisomerization.

摘要

研究了人碳酸酐酶II(HCAII)的去折叠和重折叠动力学及其被肽基脯氨酰顺/反异构酶亲环蛋白的催化作用。HCAII含有15个反式和2个顺式脯氨酰肽键,长期变性时,几乎所有未折叠分子都含有非天然脯氨酰异构体。在去折叠过程中,这些分子(Us)以双相过程缓慢产生,反映了几个反式脯氨酸和一个顺式脯氨酸的异构化。在重折叠过程中,首先快速形成熔球型中间体,随后是几次缓慢的脯氨酰异构化,这决定了再活化的速率。通过在2℃下于5.0 M盐酸胍中短暂孵育10 s,可以产生所有脯氨酸仍处于天然构象的未折叠HCAII物种(Uf)。令人惊讶的是,只有一部分Uf能快速重折叠,而其他分子重折叠缓慢。显然,一些脯氨酰肽键在重折叠早期,即在熔球阶段就发生异构化,结果,与Uf的有效折叠竞争,形成了具有不正确脯氨酰异构体的分子。当存在亲环蛋白时,这部分慢折叠分子会大量增加,因为只要分子保持在熔球状态,它就会加速非天然脯氨酰异构体的形成。随后亲环蛋白催化这些脯氨酰肽键异构化为天然状态,这些键通过进一步折叠成天然状态而在构象上得到稳定。这种催化非常有效,因为只有在熔球中可及的脯氨酸参与了这一异构化和再异构化序列。

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