Truncation studies of α-melanotropin peptides identify tripeptide analogues exhibiting prolonged agonist bioactivity

Carrie Haskell-Luevano; Tomi K. Sawyer; Siska Hendrata; Cheryl North; Laila Panahinia; Martha Stum; Douglas J. Staples; Anna M. De Lauro Castrucci; Mac E. Hadley; Victor J. Hruby

doi:10.1016/S0196-9781(96)00141-6

Truncation studies of α-melanotropin peptides identify tripeptide analogues exhibiting prolonged agonist bioactivity

Carrie Haskell-Luevano
, Tomi K. Sawyer
, Siska Hendrata
, Cheryl North
, Laila Panahinia
, Martha Stum
, Douglas J. Staples
, Anna M. De Lauro Castrucci
, Mac E. Hadley
, Victor J. Hruby

Research output: Contribution to journal › Article › peer-review

88 Scopus citations

Abstract

Systematic analysis of fragment derivatives of the superpotent α-MSH analogue, Ac-Ser-Tyr-Ser-Nle⁴-Glu-His-DPhe⁷-Arg-Trp-Gly-Lys-Pro-Val-NH₂ (NDP-MSH), led to the discovery of tripeptide agonists possessing prolonged bioactivity in the frog skin assay. Of particular significance to this discovery was Ac-DPhe-Arg-DTrp-NH₂, which was the most potent tripeptide in this series exhibiting sustained melanotropic activity. Different pharmacophore models appear to exist that are dependent on the substructure and stereochemistry of the MSH(6-9) 'active site.' The tripeptides Ac-DPhe-Arg-Trp-NH₂, Ac-DPhe-Arg-DTrp-NH₂, and Ac-DPhe-DArg-Trp-NH₂ stereochemical combinations require only Phe⁷-Xaa⁸-Trp⁹, whereas Ac-DPhe-DArg-DTrp-NH₂, Ac-Phe-Arg-DTrp-NH₂, and Ac-Phe-Arg-Trp-NH₂ additionally require His⁶ for minimal biological activity. Ac-DPhe-Arg-DTrp-NH₂ represents a novel prototype lead for the development of MSH-based peptidomimetic agonists.

Original language	English (US)
Pages (from-to)	995-1002
Number of pages	8
Journal	Peptides
Volume	17
Issue number	6
DOIs	https://doi.org/10.1016/S0196-9781(96)00141-6
State	Published - 1996
Externally published	Yes

Keywords

Ac-[Nle,DPhe]α-MSH
NDP-MSH
melanotrop in pharmacophore
melanotropin
α-MSH
α-melanocyte stimulating hormone

ASJC Scopus subject areas

Biochemistry
Physiology
Endocrinology
Cellular and Molecular Neuroscience

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10.1016/S0196-9781(96)00141-6

Cite this

@article{96da92fda31b4c988f22bcf2d9c20b0e,

title = "Truncation studies of α-melanotropin peptides identify tripeptide analogues exhibiting prolonged agonist bioactivity",

abstract = "Systematic analysis of fragment derivatives of the superpotent α-MSH analogue, Ac-Ser-Tyr-Ser-Nle4-Glu-His-DPhe7-Arg-Trp-Gly-Lys-Pro-Val-NH2 (NDP-MSH), led to the discovery of tripeptide agonists possessing prolonged bioactivity in the frog skin assay. Of particular significance to this discovery was Ac-DPhe-Arg-DTrp-NH2, which was the most potent tripeptide in this series exhibiting sustained melanotropic activity. Different pharmacophore models appear to exist that are dependent on the substructure and stereochemistry of the MSH(6-9) 'active site.' The tripeptides Ac-DPhe-Arg-Trp-NH2, Ac-DPhe-Arg-DTrp-NH2, and Ac-DPhe-DArg-Trp-NH2 stereochemical combinations require only Phe7-Xaa8-Trp9, whereas Ac-DPhe-DArg-DTrp-NH2, Ac-Phe-Arg-DTrp-NH2, and Ac-Phe-Arg-Trp-NH2 additionally require His6 for minimal biological activity. Ac-DPhe-Arg-DTrp-NH2 represents a novel prototype lead for the development of MSH-based peptidomimetic agonists.",

keywords = "Ac-[Nle,DPhe]α-MSH, NDP-MSH, melanotrop in pharmacophore, melanotropin, α-MSH, α-melanocyte stimulating hormone",

author = "Carrie Haskell-Luevano and Sawyer, \{Tomi K.\} and Siska Hendrata and Cheryl North and Laila Panahinia and Martha Stum and Staples, \{Douglas J.\} and \{De Lauro Castrucci\}, \{Anna M.\} and Hadley, \{Mac E.\} and Hruby, \{Victor J.\}",

note = "Funding Information: This work was supported by grants from the U.S. Public Health Service, DK 17420 (V.J.H.) and DK0923 1 (C.H.L.). Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the USPHS.",

year = "1996",

doi = "10.1016/S0196-9781(96)00141-6",

language = "English (US)",

volume = "17",

pages = "995--1002",

journal = "Peptides",

issn = "0196-9781",

publisher = "Elsevier Inc.",

number = "6",

}

TY - JOUR

T1 - Truncation studies of α-melanotropin peptides identify tripeptide analogues exhibiting prolonged agonist bioactivity

AU - Haskell-Luevano, Carrie

AU - Sawyer, Tomi K.

AU - Hendrata, Siska

AU - North, Cheryl

AU - Panahinia, Laila

AU - Stum, Martha

AU - Staples, Douglas J.

AU - De Lauro Castrucci, Anna M.

AU - Hadley, Mac E.

AU - Hruby, Victor J.

N1 - Funding Information: This work was supported by grants from the U.S. Public Health Service, DK 17420 (V.J.H.) and DK0923 1 (C.H.L.). Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the USPHS.

PY - 1996

Y1 - 1996

N2 - Systematic analysis of fragment derivatives of the superpotent α-MSH analogue, Ac-Ser-Tyr-Ser-Nle4-Glu-His-DPhe7-Arg-Trp-Gly-Lys-Pro-Val-NH2 (NDP-MSH), led to the discovery of tripeptide agonists possessing prolonged bioactivity in the frog skin assay. Of particular significance to this discovery was Ac-DPhe-Arg-DTrp-NH2, which was the most potent tripeptide in this series exhibiting sustained melanotropic activity. Different pharmacophore models appear to exist that are dependent on the substructure and stereochemistry of the MSH(6-9) 'active site.' The tripeptides Ac-DPhe-Arg-Trp-NH2, Ac-DPhe-Arg-DTrp-NH2, and Ac-DPhe-DArg-Trp-NH2 stereochemical combinations require only Phe7-Xaa8-Trp9, whereas Ac-DPhe-DArg-DTrp-NH2, Ac-Phe-Arg-DTrp-NH2, and Ac-Phe-Arg-Trp-NH2 additionally require His6 for minimal biological activity. Ac-DPhe-Arg-DTrp-NH2 represents a novel prototype lead for the development of MSH-based peptidomimetic agonists.

AB - Systematic analysis of fragment derivatives of the superpotent α-MSH analogue, Ac-Ser-Tyr-Ser-Nle4-Glu-His-DPhe7-Arg-Trp-Gly-Lys-Pro-Val-NH2 (NDP-MSH), led to the discovery of tripeptide agonists possessing prolonged bioactivity in the frog skin assay. Of particular significance to this discovery was Ac-DPhe-Arg-DTrp-NH2, which was the most potent tripeptide in this series exhibiting sustained melanotropic activity. Different pharmacophore models appear to exist that are dependent on the substructure and stereochemistry of the MSH(6-9) 'active site.' The tripeptides Ac-DPhe-Arg-Trp-NH2, Ac-DPhe-Arg-DTrp-NH2, and Ac-DPhe-DArg-Trp-NH2 stereochemical combinations require only Phe7-Xaa8-Trp9, whereas Ac-DPhe-DArg-DTrp-NH2, Ac-Phe-Arg-DTrp-NH2, and Ac-Phe-Arg-Trp-NH2 additionally require His6 for minimal biological activity. Ac-DPhe-Arg-DTrp-NH2 represents a novel prototype lead for the development of MSH-based peptidomimetic agonists.

KW - Ac-[Nle,DPhe]α-MSH

KW - NDP-MSH

KW - melanotrop in pharmacophore

KW - melanotropin

KW - α-MSH

KW - α-melanocyte stimulating hormone

UR - https://www.scopus.com/pages/publications/0029855290

UR - https://www.scopus.com/pages/publications/0029855290#tab=citedBy

U2 - 10.1016/S0196-9781(96)00141-6

DO - 10.1016/S0196-9781(96)00141-6

M3 - Article

C2 - 8899819

AN - SCOPUS:0029855290

SN - 0196-9781

VL - 17

SP - 995

EP - 1002

JO - Peptides

JF - Peptides

IS - 6

ER -

Truncation studies of α-melanotropin peptides identify tripeptide analogues exhibiting prolonged agonist bioactivity

Abstract

Keywords

ASJC Scopus subject areas

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