Rational modulator design by exploitation of protein-protein complex structures

被引:14
|
作者
Wichapong, Kanin [1 ]
Poelman, Hessel [1 ,2 ]
Ercig, Bogac [1 ,3 ,4 ]
Hrdinova, Johana [1 ,3 ,4 ]
Liu, Xiaosong [1 ]
Lutgens, Esther [2 ,5 ]
Nicolaes, Gerry A. F. [1 ,2 ,4 ]
机构
[1] Maastricht Univ, Cardiovasc Res Inst Maastricht CARIM, Dept Biochem, Maastricht, Netherlands
[2] Univ Amsterdam, Amsterdam Cardiovasc Sci, Amsterdam Univ Med Ctr, Dept Med Biochem,Locat AMC, Amsterdam, Netherlands
[3] Sanquin AMC Landsteiner Lab, Dept Plasma Prot, Amsterdam, Netherlands
[4] PharmaTarget BV, Maastricht, Netherlands
[5] Ludwig Maximilians Univ Munchen, Inst Cardiovasc Prevent, Munich, Germany
基金
欧洲研究理事会; 欧盟地平线“2020”;
关键词
intrinsically disordered proteins; peptide design; peptidomimetics; PPI modulators; protein-protein interactions; MOLECULAR-DYNAMICS SIMULATIONS; INTRINSICALLY DISORDERED PROTEINS; SELECTIVE SMALL-MOLECULE; PARTICLE CRYO-EM; DRUG DISCOVERY; IN-SILICO; MASS-SPECTROMETRY; BINDING-SITES; WEB SERVER; C-MYC;
D O I
10.4155/fmc-2018-0433
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The horizon of drug discovery is currently expanding to target and modulate protein-protein interactions (PPIs) in globular proteins and intrinsically disordered proteins that are involved in various diseases. To either interrupt or stabilize PPIs, the 3D structure of target protein-protein (or protein-peptide) complexes can be exploited to rationally design PPI modulators (inhibitors or stabilizers) through structure-based molecular design. In this review, we present an overview of experimental and computational methods that can be used to determine 3D structures of protein-protein complexes. Several approaches including rational and in silico methods that can be applied to design peptides, peptidomimetics and small compounds by utilization of determined 3D protein-protein/peptide complexes are summarized and illustrated.
引用
收藏
页码:1015 / 1033
页数:19
相关论文
共 50 条
  • [41] Rational design of peptide inhibitors targeting HSP90-CDC37 protein-protein interaction
    Zhang, Qiuyue
    Yan, Ling
    Zhang, Yuxuan
    Zhang, Lixiao
    Yu, Jia
    You, Qidong
    Wang, Lei
    FUTURE MEDICINAL CHEMISTRY, 2024, 16 (02) : 125 - 138
  • [42] Toward the Design of Drugs on Protein-Protein Interactions
    Sperandio, Olivier
    CURRENT PHARMACEUTICAL DESIGN, 2012, 18 (30) : 4585 - 4585
  • [43] Design of Libraries Targeting Protein-Protein Interfaces
    Fry, David
    Huang, Kuo-Sen
    Di Lello, Paola
    Mohr, Peter
    Mueller, Klaus
    So, Sung-Sau
    Harada, Takeo
    Stahl, Martin
    Vu, Binh
    Mauser, Harald
    CHEMMEDCHEM, 2013, 8 (05) : 726 - 732
  • [44] Using Designability to Design a Protein-Protein Interface
    Hannigan, Brett
    Schramm, Chaim
    Gonzalez, Gabriel
    DeGrado, William
    PROTEIN SCIENCE, 2012, 21 : 133 - 133
  • [45] Peptide design to control protein-protein interactions
    van Wier, Suzanne P.
    Beekman, Andrew M.
    CHEMICAL SOCIETY REVIEWS, 2025, 54 (04) : 1684 - 1698
  • [46] Energy functions for protein design: Adjustment with protein-protein complex affinities, models for the unfolded state, and negative design of solubility and specificity
    Pokala, N
    Handel, TM
    JOURNAL OF MOLECULAR BIOLOGY, 2005, 347 (01) : 203 - 227
  • [47] Prediction of protein-protein and protein-ligand interactions from protein structures
    Jones, D
    Sodhi, J
    Lise, S
    McGuffin, L
    Bryson, K
    FEBS JOURNAL, 2005, 272 : 397 - 398
  • [48] Protein-Protein Interaction: Prediction, Design, and Modulation
    Zhang Chang-Sheng
    Lai Lu-Hua
    ACTA PHYSICO-CHIMICA SINICA, 2012, 28 (10) : 2363 - 2380
  • [49] Structures of protein-protein complexes involved in electron transfer
    Antonyuk, Svetlana V.
    Han, Cong
    Eady, Robert R.
    Hasnain, S. Samar
    NATURE, 2013, 496 (7443) : 123 - 127
  • [50] Development and Exploitation of Photo-Crosslinking Methodology to Study Protein-Protein Interactions
    Wilson, Andrew
    JOURNAL OF PEPTIDE SCIENCE, 2018, 24 : S49 - S50