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通过用飞秒紫外激光脉冲照射活细胞来鉴定新型直接蛋白质-蛋白质相互作用。

Identification of novel direct protein-protein interactions by irradiating living cells with femtosecond UV laser pulses.

作者信息

Itri Francesco, Monti Daria Maria, Chino Marco, Vinciguerra Roberto, Altucci Carlo, Lombardi Angela, Piccoli Renata, Birolo Leila, Arciello Angela

机构信息

Department of Chemical Sciences, University of Naples Federico II, Naples 80126, Italy.

Department of Chemical Sciences, University of Naples Federico II, Naples 80126, Italy; Istituto Nazionale di Biostrutture e Biosistemi (INBB), Italy.

出版信息

Biochem Biophys Res Commun. 2017 Oct 7;492(1):67-73. doi: 10.1016/j.bbrc.2017.08.037. Epub 2017 Aug 12.

Abstract

The identification of protein-protein interaction networks in living cells is becoming increasingly fundamental to elucidate main biological processes and to understand disease molecular bases on a system-wide level. We recently described a method (LUCK, Laser UV Cross-linKing) to cross-link interacting protein surfaces in living cells by UV laser irradiation. By using this innovative methodology, that does not require any protein modification or cell engineering, here we demonstrate that, upon UV laser irradiation of HeLa cells, a direct interaction between GAPDH and alpha-enolase was "frozen" by a cross-linking event. We validated the occurrence of this direct interaction by co-immunoprecipitation and Immuno-FRET analyses. This represents a proof of principle of the LUCK capability to reveal direct protein interactions in their physiological environment.

摘要

在活细胞中识别蛋白质-蛋白质相互作用网络对于阐明主要生物学过程以及在全系统水平上理解疾病分子基础正变得越来越重要。我们最近描述了一种方法(LUCK,激光紫外交联),通过紫外激光照射在活细胞中交联相互作用的蛋白质表面。通过使用这种无需任何蛋白质修饰或细胞工程的创新方法,我们在此证明,在对HeLa细胞进行紫外激光照射后,甘油醛-3-磷酸脱氢酶(GAPDH)和α-烯醇化酶之间的直接相互作用通过交联事件被“冻结”。我们通过共免疫沉淀和免疫荧光共振能量转移(Immuno-FRET)分析验证了这种直接相互作用的发生。这代表了LUCK在其生理环境中揭示直接蛋白质相互作用能力的原理证明。

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