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N Engl J Med 389:2221-32

Small molecule proteostasis regulators that reprogram the ER to reduce extracellular protein aggregation

Overall, from an molecular energetic point of view, the formation of these three new interfacial salt bridges (Figures 3, 4 and 5) act like three electrostatic clips to further stabilize the ligand-receptor complex structure, and contribute favorably to the binding affinity of semaglutide mutant 524 to GLP-1R ECD, with the potential of the semaglutide analogue approaching, reaching and binding faster and stronger to GLP-1R ECD, and thereby leading to improved GLP-1R activation with higher efficacy and efficiency [29]

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Heart failure with mid-range or mildly reduced ejection fraction