Dose- and wavelength-dependent oxidation of crystallins by UV light--selective recognition and degradation by the 20S proteasome

Free Radic Biol Med. 1998 Jun;24(9):1369-74. doi: 10.1016/s0891-5849(98)00012-4.

Abstract

The lens of the human eye is a suitable model for age-related alterations at the molecular level. Age-related cataract formation is closely related to the accumulation of oxidatively altered proteins. In this study the influence of UV-A, UV-B, and UV-C irradiation on the proteolytic susceptibility of alpha-, betaL-, and betaH-crystallins by the isolated 20S proteasome was investigated. The proteins were irradiated with 280, 300, and 350 nm monochromatic light. Changes of the physical properties of the crystallins were characterized by absorbance measurements at 280 nm, fluorescence spectra, and SDS-PAGE-electrophoresis. The proteolytic susceptibility of crystallins was maximal after irradiation at 280 nm and three- to fivefold lower at 300 nm. Irradiation at 350 nm was not able to initiate proteolysis, probably due to protein-aggregate formation of higher molecular weight, as shown by SDS-PAGE. The damage of crystallins by UV-C light might be a signal for its proteolytic degradation by the 20S proteasome, whereas UV-B and UV-A do not increase the proteolytic susceptibility to the same extent but promote the formation of crosslinked proteins. Therefore, irradiation with UV, which is not followed by an increase in the proteolytic susceptibility, is accompanied by the formation of crosslinked proteins. It was concluded, that also long UV-B and UV-A may be involved in age-related alterations of the human lens and cataract formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Crystallins / metabolism
  • Crystallins / radiation effects*
  • Cysteine Endopeptidases / metabolism
  • Cysteine Endopeptidases / physiology*
  • Dose-Response Relationship, Radiation
  • Electrophoresis, Polyacrylamide Gel
  • Humans
  • Hydrogen Peroxide / pharmacology
  • Hydrolysis / drug effects
  • Multienzyme Complexes / metabolism
  • Multienzyme Complexes / physiology*
  • Peptide Hydrolases / metabolism
  • Proteasome Endopeptidase Complex
  • Spectrometry, Fluorescence
  • Ultraviolet Rays*

Substances

  • Crystallins
  • Multienzyme Complexes
  • Hydrogen Peroxide
  • Peptide Hydrolases
  • Cysteine Endopeptidases
  • Proteasome Endopeptidase Complex