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

被引:4
|
作者
Itri, Francesco [1 ]
Monti, Dania Maria [1 ,2 ]
Chino, Marco [1 ]
Vinciguerra, Roberto [1 ]
Altucci, Carlo [3 ,4 ]
Lombardi, Angela [1 ]
Piccoli, Renata [1 ,2 ]
Birolo, Leila [1 ]
Arciello, Angela [1 ,2 ]
机构
[1] Univ Naples Federico II, Dept Chem Sci, I-80126 Naples, Italy
[2] INBB, Naples, Italy
[3] Univ Naples Federico II, Dept Phys Ettore Pancini, I-80126 Naples, Italy
[4] Consorzio Nazl Interuniv Sci Fis Mat CNISM, UdR, Naples, Italy
关键词
Protein-protein interactions; Ultrashort UV laser pulses; UV cross-linking; Living cells irradiation; Metabolic nanomachines; FAST INTERACTION REFINEMENT; CROSS-LINKING; GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE; GLYCOLYTIC ENZYME; MASS-SPECTROMETRY; MOLECULAR DOCKING; FIREDOCK;
D O I
10.1016/j.bbrc.2017.08.037
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:67 / 73
页数:7
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