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A 类 G 蛋白偶联受体中肽结合的结构基础。

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

机构信息

Deparment of Chemistry, Vanderbilt University, Nashville, TN 37235, USA.

Center for Structural Biology, Vanderbilt University, Nashville, TN 37232, USA.

出版信息

Molecules. 2021 Dec 30;27(1):210. doi: 10.3390/molecules27010210.

Abstract

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.

摘要

G 蛋白偶联受体(GPCRs)是最大的膜蛋白家族之一,也是治疗药物的重要靶标类别。GPCRs 中最大的 A 类受体几乎影响人类生理学的各个方面。该家族约 45%的成员内源性结合灵活的肽或较大蛋白质配体中的肽段。虽然这些肽中的许多已经在其溶液状态下进行了结构表征,但对其受体结合状态下的肽的少数研究表明,这些肽与一组共享的残基相互作用,并经历显著的构象变化。为了了解结合动力学和肽模拟药物化合物的开发,应该进一步研究与同源受体复合的肽配体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9660/8746363/6806c2704450/molecules-27-00210-g001.jpg

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