肽
化学
胰高血糖素样肽-1
合理设计
胰高血糖素样肽-2
普吕卡贡
受体
药物发现
小分子
G蛋白偶联受体
计算生物学
药理学
生物化学
内分泌学
生物
纳米技术
糖尿病
2型糖尿病
材料科学
作者
Rie Suzuki,Giles A. Brown,J.A. Christopher,Conor C. G. Scully,Miles Congreve
标识
DOI:10.1021/acs.jmedchem.9b00835
摘要
Glucagon-like peptide 1 (GLP-1) and glucagon-like peptide 2 (GLP-2) are proglucagon derived peptides that are released from gut endocrine cells in response to nutrient intake. These molecules are rapidly inactivated by the action of dipeptidyl peptidase IV (DPP-4) which limits their use as therapeutic agents. The recent emergence of three-dimensional structures of GPCRs such as GLP-1R and glucagon receptor has helped to drive the rational design of innovative peptide molecules that hold promise as novel peptide therapeutics. One emerging area is the discovery of multifunctional molecules that act at two or more pharmacological systems to enhance therapeutic efficacy. In addition, drug discovery efforts are also focusing on strategies to improve patient convenience through alternative routes of peptide delivery. These novel strategies highlight the broad utility of peptide-based therapeutics in human disease settings where unmet needs still exist.
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