Extended Metadynamics Protocol for Binding/Unbinding Free Energies of Peptide Ligands to Class A G-Protein-Coupled Receptors

被引:3
|
作者
Calderon, Jacqueline C. [1 ]
Plut, Eva [2 ]
Keller, Max [3 ]
Cabrele, Chiara [2 ]
Reiser, Oliver [2 ]
Gervasio, Francesco L. [4 ]
Clark, Timothy [1 ]
机构
[1] Friedrich Alexander Univ Erlangen Nuernberg, Comp Chem Ctr, Dept Chem & Pharm, D-91052 Erlangen, Germany
[2] Univ Regensburg, Inst Organ Chem, Fac Chem & Pharm, D-93040 Regensburg, Germany
[3] Univ Regensburg, Inst Pharm, Fac Chem & Pharm, D-93040 Regensburg, Germany
[4] Univ Geneva, Pharmaceut Sci, CH-1211 Geneva, Switzerland
关键词
NEUROPEPTIDE-Y; UCSF CHIMERA; N-TERMINUS; BINDING; NEUROTENSIN; DISCOVERY; AFFINITY; ARGININE; VISUALIZATION; PHARMACOLOGY;
D O I
10.1021/acs.jcim.3c01574
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A metadynamics protocol is presented to characterize the binding and unbinding of peptide ligands to class A G-protein-coupled receptors (GPCRs). The protocol expands on the one previously presented for binding and unbinding small-molecule ligands to class A GPCRs and accounts for the more demanding nature of the peptide binding-unbinding process. It applies to almost all class A GPCRs. Exemplary simulations are described for subtypes Y1R, Y2R, and Y4R of the neuropeptide Y receptor family, vasopressin binding to the vasopressin V-2 receptor (V2R), and oxytocin binding to the oxytocin receptor (OTR). Binding free energies and the positions of alternative binding sites are presented and, where possible, compared with the experiment.
引用
收藏
页码:205 / 218
页数:14
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