کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
443637 | 692742 | 2013 | 10 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Exploring the effect of PARP-1 flexibility in docking studies Exploring the effect of PARP-1 flexibility in docking studies](/preview/png/443637.png)
• We used REMD simulations to sample the conformational space of ligand-bound and unbound PARP-1.
• We observed the formation of an accessory pocket in the catalytic cleft of PARP-1.
• The selection of a PARP-1 conformation containing the accessory pocket improves the results of docking studies.
• This study highlights the beneficial effect of incorporating PARP-1 flexibility in docking studies of PARP-1 ligands.
Poly(ADP-ribose)polymerase-1 (PARP-1) is an enzyme belonging to the ADP-ribosyltransferase family. A large body of works has validated PARP-1 as an attractive drug target for different therapeutic areas, including cancers and ischemia. Accordingly, sampling the conformational space of the enzyme is pivotal to understand its functions and improve structure-based drug discovery approaches.In the first part of this study we apply replica exchange molecular dynamic (REMD) simulations to sample the conformational space of the catalytic domain of PARP-1 in the ligand-bound and unbound forms. In the second part, we assess how and to what extend the emerging enzyme flexibility affects the performance of docking experiments of a library of PARP-1 inhibitors. This study pinpoints a putative key role of conformational shifts of Leu324, Tyr325 and Lys242 in opening an additional binding site pocket that affects the binding of ligands to the catalytic cleft of PARP-1. Furthermore, it highlights the improvement of the enrichment factor of active ligands obtained in docking experiments when using conformations generated with REMD simulations of ligand-bound PARP-1.
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Journal: Journal of Molecular Graphics and Modelling - Volume 45, September 2013, Pages 192–201