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PERRC:通过反应物停留时间控制进行蛋白酶工程

PERRC: Protease Engineering with Reactant Residence Time Control.

作者信息

Nelson Sage, Gaza Jokent, Ajayebi Seyednima, Masse Ronald, Pho Raymond, Scutero Cianna, Martinusen Samantha, Long Lawton, Menezes Amor, Perez Alberto, Denard Carl

机构信息

Department of Chemical Engineering, University of Florida, Gainesville 32611, United States.

Department of Chemistry, University of Florida, Gainesville 32611, United States.

出版信息

ACS Synth Biol. 2025 Jun 20;14(6):2241-2253. doi: 10.1021/acssynbio.5c00154. Epub 2025 May 19.

Abstract

Proteases with engineered specificity hold great potential for targeted therapeutics, protein circuit construction, and biotechnology applications. However, many proteases exhibit broad substrate specificity, limiting their use in such applications. Engineering protease specificity remains challenging because evolving a protease to recognize a new substrate, without counterselecting against its native substrate, often results in high residual activity on the original substrate. To address this, we developed Protease Engineering with Reactant Residence Time Control (PERRC), a platform that exploits the correlation between endoplasmic reticulum (ER) retention sequence strength and ER residence time. PERRC allows precise control over the stringency of protease evolution by adjusting counterselection to selection substrate ratios. Using PERRC, we evolved an orthogonal tobacco etch virus protease variant, TEVESNp, that selectively cleaves a substrate (ENLYFES) that differs by only one amino acid from its parent sequence (ENLYFQS). TEVESNp exhibits a remarkable 65-fold preference for the evolved substrate, marking the first example of an engineered orthogonal protease driven by such a slight difference in substrate recognition. Furthermore, TEVESNp functions as a competent protease for constructing orthogonal protein circuits in bacteria, and molecular dynamics simulations analysis reveals subtle yet functionally significant active site rearrangements. PERRC is a modular dual-substrate display system that facilitates precise engineering of protease specificity.

摘要

具有工程化特异性的蛋白酶在靶向治疗、蛋白质电路构建和生物技术应用方面具有巨大潜力。然而,许多蛋白酶表现出广泛的底物特异性,限制了它们在此类应用中的使用。工程化蛋白酶特异性仍然具有挑战性,因为在不针对其天然底物进行反选择的情况下,使蛋白酶进化以识别新底物通常会导致其对原始底物具有较高的残留活性。为了解决这个问题,我们开发了反应物停留时间控制的蛋白酶工程(PERRC),这是一个利用内质网(ER)保留序列强度与ER停留时间之间的相关性的平台。PERRC通过调整反选择与选择底物的比例,允许对蛋白酶进化的严格程度进行精确控制。使用PERRC,我们进化出了一种正交烟草蚀纹病毒蛋白酶变体TEVESNp,它选择性地切割一种底物(ENLYFES),该底物与其亲本序列(ENLYFQS)仅相差一个氨基酸。TEVESNp对进化后的底物表现出显著的65倍偏好,这标志着由底物识别上如此微小的差异驱动的工程化正交蛋白酶的首个实例。此外,TEVESNp作为一种适用于在细菌中构建正交蛋白质电路的蛋白酶发挥作用,并且分子动力学模拟分析揭示了细微但功能上重要的活性位点重排。PERRC是一个模块化双底物展示系统,有助于对蛋白酶特异性进行精确工程设计。

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