Characterization of new D-beta-aspartate-containing proteins in a lens-derived cell line

Biochem Biophys Res Commun. 2005 Sep 9;334(4):1022-31. doi: 10.1016/j.bbrc.2005.06.195.

Abstract

Although proteins are generally composed of l-alpha-amino acids, biologically uncommon D-beta-aspartic acid (Asp)-containing proteins have been reported in various tissues from elderly individuals. Our previous study indicated that the N/N1003A cell line, derived from rabbit lens, includes D-beta-Asp-containing proteins of approximately 50 kDa by Western blot analysis of a 2D-gel using a polyclonal antibody that is highly specific for D-beta-Asp-containing proteins. In this study, we identified the D-beta-Asp-containing proteins by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry and the Mascot online database searching algorithm. The results indicate that one of these 50 kDa proteins is an enolase showing homology with tau-crystallin. Other D-beta-Asp-containing proteins, which we have recently discovered include lamin A/C, cytoplasmic NADP+-dependent isocitrate dehydrogenase, fructose-bisphosphate aldolase A, aldose reductase, L-lactate dehydrogenase A or calponin H2, phosphoglycerate mutase 1, phosphatidylethanolamine-binding protein, alpha-B-crystallin, and peptidyl-prolyl cis-trans isomerase A (PPlase).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Crystallins / chemistry*
  • Crystallins / metabolism*
  • Isoaspartic Acid / chemistry*
  • Isoaspartic Acid / metabolism*
  • Lens, Crystalline / chemistry*
  • Lens, Crystalline / metabolism*
  • Molecular Weight
  • Rabbits

Substances

  • Crystallins
  • Isoaspartic Acid