The Structural Basis of Peptide Binding at Class A G Protein-Coupled Receptors

被引:12
|
作者
Vu, Oanh [1 ,2 ]
Bender, Brian Joseph [2 ,3 ]
Pankewitz, Lisa [2 ]
Huster, Daniel [4 ]
Beck-Sickinger, Annette G. [5 ]
Meiler, Jens [1 ,2 ,3 ,6 ,7 ]
机构
[1] Vanderbilt Univ, Dept Chem, Box 1583, Nashville, TN 37235 USA
[2] Vanderbilt Univ, Struct Biol Ctr, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Dept Pharmacol, Nashville, TN 37232 USA
[4] Univ Leipzig, Inst Med Phys & Biophys, Dept Med, Hartelstr 16-18, D-04107 Leipzig, Germany
[5] Univ Leipzig, Inst Biochem, Fac Life Sci, Bruderstr 34, D-04103 Leipzig, Germany
[6] Univ Leipzig, Med Ctr, Inst Drug Discovery, Dept Chem, Bruderstr 34, D-04103 Leipzig, Germany
[7] Univ Leipzig, Med Ctr, Inst Drug Discovery, Dept Comp Sci, Bruderstr 34, D-04103 Leipzig, Germany
来源
MOLECULES | 2022年 / 27卷 / 01期
关键词
peptide GPCR; class A GPCR; peptide docking; non-canonical amino acids; NUCLEAR-MAGNETIC-RESONANCE; 3-DIMENSIONAL CONSENSUS STRUCTURE; GONADOTROPIN-RELEASING-HORMONE; RESOLUTION CRYSTAL-STRUCTURE; LOW-ENERGY CONFORMATIONS; AMINO-ACID-SEQUENCE; SOLID-STATE NMR; NEUROPEPTIDE-Y; OPIOID RECEPTOR; CHEMOKINE RECOGNITION;
D O I
10.3390/molecules27010210
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
G protein-coupled receptors (GPCRs) represent the largest membrane protein family and a significant target class for therapeutics. Receptors from GPCRs' largest class, class A, influence virtually every aspect of human physiology. About 45% of the members of this family endogenously bind flexible peptides or peptides segments within larger protein ligands. While many of these peptides have been structurally characterized in their solution state, the few studies of peptides in their receptor-bound state suggest that these peptides interact with a shared set of residues and undergo significant conformational changes. For the purpose of understanding binding dynamics and the development of peptidomimetic drug compounds, further studies should investigate the peptide ligands that are complexed to their cognate receptor.
引用
收藏
页数:24
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