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In this work, we investigate the molecular mechanisms by which GLP-1, oxyntomodulin, exendin-4, and exendin-P5 bind and activate the GLP-1R using a combination of structural biology, molecular dynamics simulations, and pharmacological studies combined with extensive receptor mutagenesis

18 GLP-1R activation in endothelial cells results in the expression of more endothelial nitric oxide synthase, providing greater amounts of nitric oxide and consequent vasodilation

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With the rise of emerging therapeutic modalities, such as complex biologics, immune cell therapies and gene therapies, how are CDMOs adapting their fill/finish capabilities to meet evolving client needs