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Dipeptidyl peptidase-4: difference between revisions

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Revision 12 — 18:12, 3 Dec 2024
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Revision 13 — 04:50, 26 Dec 2024
ColdChainCleo (talk)
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39| Fusion partner | [[Dulaglutide]] | Fc domain, plus Gly substitution |39| Fusion partner | [[Dulaglutide]] | Fc domain, plus Gly substitution |
4040
+41Substitution alone is not sufficient for a long dosing interval — a DPP-4-resistant peptide is still cleared renally within hours — so the resistant residue is almost always combined with an [[Albumin binding half-life extension|albumin-binding]] or fusion strategy. Semaglutide combines both, and adds a substitution at position 34 to prevent acylation at the wrong lysine.{{r|knudsen2019}}
+42
41== References ==43== References ==
42{{reflist}}44{{reflist}}
43<ref name="deacon2019">Deacon CF. "Physiology and pharmacology of DPP-4 in glucose homeostasis and the treatment of type 2 diabetes." ''Frontiers in Endocrinology'' 10:80 (2019). DOI:10.3389/fendo.2019.00080. PMID 30828317.</ref>45<ref name="deacon2019">Deacon CF. "Physiology and pharmacology of DPP-4 in glucose homeostasis and the treatment of type 2 diabetes." ''Frontiers in Endocrinology'' 10:80 (2019). DOI:10.3389/fendo.2019.00080. PMID 30828317.</ref>
44<ref name="holst2007">Holst JJ. "The physiology of glucagon-like peptide 1." ''Physiological Reviews'' 87(4):1409–1439 (2007). PMID 17928588.</ref>46<ref name="holst2007">Holst JJ. "The physiology of glucagon-like peptide 1." ''Physiological Reviews'' 87(4):1409–1439 (2007). PMID 17928588.</ref>
+47<ref name="knudsen2019">Knudsen LB, Lau J. "The discovery and development of liraglutide and semaglutide." ''Frontiers in Endocrinology'' 10:155 (2019). PMID 31031702.</ref>
4548
46== See also ==49== See also ==