Targeting intrinsically disordered proteins in rational drug discovery

被引:73
作者
Ambadipudi, Susmitha [1 ]
Zweckstetter, Markus [1 ,2 ,3 ]
机构
[1] German Ctr Neurodegenerat Dis DZNE, D-37077 Gottingen, Germany
[2] Max Planck Inst Biophys Chem, Dept NMR Based Struct Biol, D-37077 Gottingen, Germany
[3] Univ Med Ctr Groningen, DFG Res Ctr Nanoscale Microscopy & Mol Physiol Br, D-37073 Gottingen, Germany
关键词
drug discovery; intrinsically disordered protein; neurodegeneration; NMR spectroscopy; SINGLE-MOLECULE SPECTROSCOPY; ALPHA-SYNUCLEIN; ALZHEIMERS-DISEASE; NMR-SPECTROSCOPY; TAU-PROTEIN; C-MYC; PARKINSONS-DISEASE; UNFOLDED PROTEINS; CONFORMATIONAL PROPERTIES; UNSTRUCTURED PROTEINS;
D O I
10.1517/17460441.2016.1107041
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Intrinsically disordered proteins (IDPs) and intrinsically disordered protein regions (IDPRs) have gained wide recognition over the past decade due to their versatile roles in cell physiology and pathology. A large repertoire of IDPs/IDPRs has been implicated in numerous diseases, making them potential targets for therapeutic intervention. Recent advances in experimental methods and computational approaches have enabled detection and characterization of these highly dynamic proteins at atomistic detail, thus facilitating disorder/dynamic-based drug discovery.Areas covered: This article presents an overview of the functional relevance and pathological implications of IDPs/IDPRs in cells. The authors outline the currently available experimental methods employed for structural characterization of these proteins. They also exemplify the practical limitations encountered during such characterization and ways to overcome them. Taken together, the article discusses the plausibility of exploiting protein disorder for drug targeting.Expert opinion: Disorder-based drug targeting is gearing up in the realm of novel drug discovery approaches. Tools for probing the molecular features of IDPs and IDPRs are rapidly improving and start to provide accurate descriptions of the complex ensembles populated by IDPs/IDPRs. They thus pave the way for the development of drug molecules, which specifically target disease-associated disorder.
引用
收藏
页码:65 / 77
页数:13
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