共 50 条
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.
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页码:1015 / 1033
页数:19
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