Retrocyclins: Using Past as Prologue

Author(s): Alexander M. Cole, Wei Wang, Alan J. Waring, Robert I. Lehrer

Journal Name: Current Protein & Peptide Science

Volume 5 , Issue 5 , 2004

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Retrocyclins are synthetic θdefensins that were reconstructed from genetic blueprints that had remained unused for at least 7.5 million years. From phylogenetic studies, it appears that θdefensins arose in Old World Monkeys, after that lineage had separated from the prosimians and New World Monkeys. Although some nonhuman primates continue to produce θdefensin peptides today, Homo sapiens and his gorilla, bonobo, and chimpanzee relatives do not. Their inability to do so reflects the common inheritance of defective θdefensin genes which contain a premature stop codon that aborts translation. We can only speculate if this ancient genetic event has any contemporary relevance. However, it is noteworthy that synthetic retrocyclins can prevent the entry of HIV-1 and other viruses (e.g., HSV-2) into otherwise susceptible human target cells. Our studies suggest that their antiviral properties are intimately linked to an ability to bind carbohydrate epitopes displayed by viral and cell-surface glycoproteins involved in viral entry. The ability of retrocyclins to recognize and bind carbohydrate and glycan moieties is shared by θdefensins (RTDs) from rhesus monkeys and by several - but not all - human αdefensins. In addition to being the only cyclic peptides of animal origin, the lectin-like activity of θdefensins gives them the added distinction of being the smallest sugar-binding molecules of natural origin identified to date. This unusual combination makes θdefensins intriguing molecular prototypes that could be used to design novel carbohydrate-binding or antiviral agents.

Keywords: antiviral, cyclic peptides, hiv-1 uptake inhibitors, lectin, retrocyclin, theta-defensin

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Article Details

Year: 2004
Page: [373 - 381]
Pages: 9
DOI: 10.2174/1389203043379657
Price: $65

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