Steroidogenic activity of a peptide specified by the reversed sequence of corticotropin mRNA

Benjamin L. Clarke, J. Edwin Blalock

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

The molecular recognition theory predicts that a reversed (3′→5′) reading of an mRNA should yield a peptide that is structurally and functionally similar to that specified in the 5′→3′ direction. We tested this idea by synthesizing a corticotropin (ACTH) analogue using a reverse reading of bovine mRNA for ACTH-(1-24). This peptide, designated ACTH-3′→5′, had a similar hydropathic profile to native ACTH- 5′→3′ but had only 30% sequence homology and eight different charge substitutions. ACTH-3′→5′ specifically bound to the surface of mouse Y-1 adrenal cells and to polyclonal anti-ACTH antibody. Additionally, ACTH-3′→5′ stimulated cAMP synthesis and steroidogenesis in adrenal cells. These findings show that ACTH-3′→5′ mimics the corticotropic properties of native ACTH, thereby further validating the molecular recognition theory.

Original languageEnglish (US)
Pages (from-to)9708-9711
Number of pages4
JournalProceedings of the National Academy of Sciences of the United States of America
Volume87
Issue number24
StatePublished - 1990

Keywords

  • Antisense peptide
  • Complementary peptide
  • Molecular code
  • Molecular recognition theory
  • Peptide mimetic

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