Studies of conformational isomerism in α-melanocyte stimulating hormone by design of cyclic analogues

G. V. Nikiforovich, S. D. Sharma, M. E. Hadley, V. J. Hruby

Research output: Contribution to journalArticle

20 Scopus citations

Abstract

Results of energy calculations for α-MSH (α-melanocyte stimulating hormone, Ac-Ser1-Tyr2-Ser3-Met4-Glu 5-His6-Phe7-Arg8-Trp 9-Gly10-Lys11-Pro12-Val 13-NH2) and [D-Phe7]α-MSH were used for design of cyclic peptides with the general aim to stabilize different conformational isomers of the parent compound. The minimal structural modifications of the conformationally flexible Gly10 residue, as substitutions for L-Ala, D-Ala, or Aib (replacing of hydrogen atoms by methyl groups), were applied to obtain octa- and heptapeptide analogues of α-MSH(4-11) and α-MSH (5-11), which were cyclized by lactam bridges between the side chains in positions 5 and 11. Some of these analogues, namely those with substitutions of the Gly10 residue with L-Ala or Aib, showed biological activity potencies on frog skin comparable to the potency of the parent tridecapeptide hormone. Additional energy calculations for designed cyclic analogues were used for farther refinement of the model for the biologically active conformations of the His-PheArg-Trp "message" sequence within the sequences of α-MSH and [D-Phe7] α-MSH. In such conformations the aromatic moieties of the side chains of the His6, L/D-Phe7, and Trp9 residues form a continuous hydrophobic "surface,"presumably interacting with a complementary receptor site. This feature is characteristic for low-energy conformers of active cyclic analogues, but it is absent in the case of inactive analogues. This particular spatial arrangement of functional groups involved in the message sequence is very close for α-MSH and [D-Phe7]α-MSH, as well as for biologically active cyclic analogues despite differences of dihedral angle values for corresponding low-energy conformations.

Original languageEnglish (US)
Pages (from-to)155-167
Number of pages13
JournalBiopolymers
Volume46
Issue number3
StatePublished - Dec 1 1998

Keywords

  • Cyclic analogues
  • Isomerism
  • [d-Phe]α-MSH
  • α-MSH

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Biomaterials
  • Organic Chemistry

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