Conformational study of insect adipokinetic hormones using NMR constrained molecular dynamics |
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Authors: | Margie M. Nair Graham E. Jackson Gerd Gäde |
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Affiliation: | (1) Department of Chemistry, University of Cape Town, Private Bag, Rondebosch, Cape Town, 7701, South Africa;(2) Department of Zoology, University of Cape Town, Private Bag, Rondebosch, Cape Town, 7701, South Africa |
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Abstract: | Mem-CC (pGlu-Leu-Asn-Tyr-Ser-Pro-Asp-Trp-NH2), Tem-HrTH (pGlu-Leu-Asn-Phe-Ser-Pro-Asn-Trp-NH2) and Del-CC (pGlu-Leu-Asn-Phe-Ser-Pro-Asn-Trp-Gly-Asn-NH2) are adipokinetic hormones, isolated from the corpora cardiaca of different insect species. These hormones regulate energy metabolism during flight and so are intimately involved in an insect's mobility. Secondary structural elements of these peptides and the N7 analogue, [N7]-Mem-CC (pGlu-Leu-Asn-Tyr-Ser-Pro-Asn-Trp-NH2), have been determined in dimethylsulfoxide solution using NMR restrained molecular mechanic simulations. The neuropeptides were all found to have an extended structure for the first 4 residues and a -turn between residues 4–8. For Tem-HrTH and Del-CC, asparagine (N7) which is postulated to be involved in receptor binding and/or activation, projects outward form the -turn. Mem-CC does not have an asparagine at position 7 while, for [N7]-Mem-CC, the N7 sidechain folds inside the -turn preventing its interaction with the receptor. |
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Keywords: | AKH/RPCH peptides Del-CC Mem-CC [N7]-Mem-CC Tem-HrTH Solution conformation |
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