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沿着反应中心环的单个荧光探针揭示了纤溶酶原激活物抑制剂-1潜伏转变过程中的位点特异性变化。

Single fluorescence probes along the reactive center loop reveal site-specific changes during the latency transition of PAI-1.

作者信息

Qureshi Tihami, Peterson Cynthia B

机构信息

Department of Biochemistry, Cellular and Molecular Biology, University of Tennessee, Knoxville, Tennessee, 37996.

出版信息

Protein Sci. 2016 Feb;25(2):487-98. doi: 10.1002/pro.2839. Epub 2015 Nov 25.

Abstract

The serine protease inhibitor (serpin), plasminogen activator inhibitor-1 (PAI-1), is an important biomarker for cardiovascular disease and many cancers. It is therefore a desirable target for pharmaceutical intervention. However, to date, no PAI-1 inhibitor has successfully reached clinical trial, indicating the necessity to learn more about the mechanics of the serpin. Although its kinetics of inhibition have been extensively studied, less is known about the latency transition of PAI-1, in which the solvent-exposed reactive center loop (RCL) inserts into its central β-sheet, rendering the inhibitor inactive. This spontaneous transition is concomitant with a large translocation of the RCL, but no change in covalent structure. Here, we conjugated the fluorescent probe, NBD, to single positions along the RCL (P13-P5') to detect changes in solvent exposure that occur during the latency transition. The results support a mousetrap-like RCL-insertion that occurs with a half-life of 1-2 h in accordance with previous reports. Importantly, this study exposes unique transitions during latency that occur with a half-life of ∼5 and 25 min at the P5' and P8 RCL positions, respectively. We hypothesize that the process detected at P5' represents s1C detachment, while that at P8 results from a steric barrier to RCL insertion. Together, these findings provide new insights by characterizing multiple steps in the latency transition.

摘要

丝氨酸蛋白酶抑制剂(serpin),纤溶酶原激活物抑制剂-1(PAI-1),是心血管疾病和许多癌症的重要生物标志物。因此,它是药物干预的理想靶点。然而,迄今为止,尚无PAI-1抑制剂成功进入临床试验,这表明有必要更多地了解serpin的作用机制。尽管其抑制动力学已得到广泛研究,但对于PAI-1的潜伏转变了解较少,在潜伏转变过程中,暴露于溶剂中的反应中心环(RCL)插入其中心β-折叠,使抑制剂失活。这种自发转变伴随着RCL的大量移位,但共价结构没有变化。在这里,我们将荧光探针NBD连接到RCL(P13-P5')沿线的单个位置,以检测潜伏转变过程中发生的溶剂暴露变化。结果支持了一种类似捕鼠器的RCL插入,其半衰期为1-2小时,与先前的报道一致。重要的是,这项研究揭示了潜伏期间独特的转变,分别在P5'和P8 RCL位置以约5分钟和25分钟的半衰期发生。我们假设在P5'处检测到的过程代表s1C分离,而在P8处的过程是由于RCL插入的空间位垒。总之,这些发现通过表征潜伏转变中的多个步骤提供了新的见解。

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本文引用的文献

1
Serpin latency transition at atomic resolution.丝氨酸蛋白酶抑制剂在原子分辨率下的潜伏态转变。
Proc Natl Acad Sci U S A. 2014 Oct 28;111(43):15414-9. doi: 10.1073/pnas.1407528111. Epub 2014 Oct 13.

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