Peptidomics and genomics analysis of novel antimicrobial peptides from the frog, Rana nigrovittata

Genomics. 2010 Jan;95(1):66-71. doi: 10.1016/j.ygeno.2009.09.004. Epub 2009 Sep 22.

Abstract

Much attention has been paid on amphibian peptides for their wide-ranging pharmacological properties, clinical potential, and gene-encoded origin. More than 300 antimicrobial peptides (AMPs) from amphibians have been studied. Peptidomics and genomics analysis combined with functional test including microorganism killing, histamine-releasing, and mast cell degranulation was used to investigate antimicrobial peptide diversity. Thirty-four novel AMPs from skin secretions of Rana nigrovittata were identified in current work, and they belong to 9 families, including 6 novel families. Other three families are classified into rugosin, gaegurin, and temporin family of amphibian AMP, respectively. These AMPs share highly conserved preproregions including signal peptides and spacer acidic peptides, while greatly diversified on mature peptides structures. In this work, peptidomics combined with genomics analysis was confirmed to be an effective way to identify amphibian AMPs, especially novel families. Some AMPs reported here will provide leading molecules for designing novel antimicrobial agents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Amphibian Proteins / chemistry*
  • Amphibian Proteins / classification
  • Amphibian Proteins / genetics*
  • Amphibian Proteins / pharmacology
  • Animals
  • Anti-Infective Agents / pharmacology
  • Candida albicans / drug effects
  • Erythrocytes / drug effects
  • Female
  • Genomics*
  • Gram-Negative Bacteria / drug effects
  • Gram-Positive Bacteria / drug effects
  • Male
  • Mast Cells / drug effects
  • Microbial Sensitivity Tests
  • Molecular Sequence Data
  • Peptides / chemistry*
  • Peptides / classification
  • Peptides / genetics*
  • Peptides / pharmacology
  • Proteomics*
  • Rabbits
  • Ranidae / genetics
  • Rats
  • Sequence Analysis, Protein
  • Skin / chemistry

Substances

  • Amphibian Proteins
  • Anti-Infective Agents
  • Peptides