Molecular insights into the stabilization of protein-protein interactions with small molecule: The FKBP12-rapamycin-FRB case study

被引:8
作者
Chaurasia, Shilpi [1 ]
Pieraccini, Stefano [1 ,2 ,3 ]
De Gonda, Riccardo [1 ]
Conti, Simone [1 ]
Sironi, Maurizio [1 ,2 ,3 ]
机构
[1] Univ Milan, Dipartimento Chim, I-20133 Milan, Italy
[2] ISTM CNR, Ist Sci & Tecnol Mol, I-20133 Milan, Italy
[3] Ist Sci & Tecnol Mat INSTM UdR, Milan, Italy
关键词
FREE-ENERGY DECOMPOSITION; BINDING-PROTEIN; RAPAMYCIN; SIROLIMUS; INTEGRATION; INHIBITION; PRINCIPLES; MECHANISM; DYNAMICS; COMPLEX;
D O I
10.1016/j.cplett.2013.09.042
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
Targetting protein-protein interactions is a challenging task in drug discovery process. Despite the challenges, several studies provided evidences for the development of small molecules modulating protein-protein interactions. Here we consider a typical case of protein-protein interaction stabilization: the complex between FKBP12 and FRB with rapamycin. We have analyzed the stability of the complex and characterized its interactions at the atomic level by performing free energy calculations and computational alanine scanning. It is shown that rapamycin stabilizes the complex by acting as a bridge between the two proteins; and the complex is stable only in the presence of rapamycin. (C) 2013 Elsevier B. V. All rights reserved.
引用
收藏
页码:68 / 74
页数:7
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