Home LiteratureArticle Details
PMID: 501285 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Nonenzymatic glycosylation, sulfhydryl oxidation, and aggregation of lens proteins in experimental sugar cataracts.

The Journal of experimental medicine ·Vol. 150 ·No. 5 ·1979-11-01 ·Pages 1098-107

Monnier VM, Stevens VJ, Cerami A

Abstract

The formation of sugar-cataracts has been hypothesized to involve the nonenzymatic glycosylation, sulfhydryl oxidation, and aggregation of lens proteins. Cataractous lenses of diabetic and galactosemic rats were analyzed for glycosylated lysine residues in crystallins. A five- and a ten-fold increase in glycosylated lysine residues was measured in galactose and diabetic cataracts, respectively. The modification was predominant in the insoluble fraction of the lens homogenate. The proteins were further examined for the presence of disulfide bonds and high molecular weight aggregates. After careful disruption of the lens in a nitrogen environment, a cloudy solution was obtained from cataractous lenses whereas a clear solution was obtained from normal lenses. The absorbance at 550 nm of the solution of both the galactosemic and the diabetic cataracts could be decreased by approximately 50% with the addition of dithioerythritol (50 mM). The presence of high molecular weight aggregates was ascertained by sucrose gradient centrifugation and gel filtration chromatography. The proteins were heterogenous in size and showed a mol wt range of 36 to greater than 176 million daltons. Treatment with dithioerythritol induced a marked decrease in the amount of high molecular weight proteins. These data suggest that sugar cataracts of experimental animals have, in common with human cataracts, the presence of high molecular weight aggregates which are in part linked by disulfide bonds.

MeSH Terms
Alloxan Animals Cataract/complications,metabolism Centrifugation, Density Gradient Chromatography, Gel Crystallins/metabolism Diabetes Mellitus, Experimental/complications Female Galactosemias/complications Lysine/metabolism Oxidation-Reduction Rats Sulfhydryl Compounds/metabolism
Chemicals
Crystallins Sulfhydryl Compounds Alloxan Lysine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Monnier V M
Stevens V J
Cerami A
References (16)
16 references, click to expand
  1. Protein measurement with the Folin phenol reagent.
    J Biol Chem. 1951 Nov;193(1):265-75 PMID: 14907713
  2. Studies on the oxidation of cysteine to cystine in lens proteins during cataract formation.
    Am J Ophthalmol. 1951 May;34(5:2):104-13 PMID: 14829519
  3. An extrinsic membrane polypeptide associated with high-molecular-weight protein aggregates in human cataract.
    Science. 1979 Jun 22;204(4399):1323-6 PMID: 377484
  4. Diabetic cataract formation: potential role of glycosylation of lens crystallins.
    Proc Natl Acad Sci U S A. 1978 Jun;75(6):2918-22 PMID: 275862
  5. Characterization of lens proteins. II. gamma-Crystallin of normal and cataractous rat lenses.
    Exp Eye Res. 1978 Mar;26(3):255-65 PMID: 639878
  6. The state of sulphydryl groups in normal and cataractous human lenses.
    Exp Eye Res. 1977 Aug;25(2):139-48 PMID: 913506
  7. Proteins containing reductively aminated disaccharides. Synthesis and chemical characterization.
    Arch Biochem Biophys. 1977 Jun;181(2):542-9 PMID: 900934
  8. Characterization of lens proteins I. Identification of additional soluble fractions in rat lenses.
    Exp Eye Res. 1977 Apr;24(4):355-67 PMID: 858318
  9. Isolation and characterizaion of covalently linked, high molecular weight proteins from human cataractous lens.
    Exp Eye Res. 1977 Jan;24(1):63-70 PMID: 838003
  10. Mechanisms initiating cataract formation. Proctor Lecture.
    Invest Ophthalmol. 1974 Oct;13(10):713-24 PMID: 4278188
  11. Age-dependent changes in the molecular size of human lens proteins and their relationship to light scatter.
    Invest Ophthalmol. 1974 Oct;13(10):795-8 PMID: 4411898
  12. Disulphide cross-linked protein of high molecular weight in human cataractous lens.
    Exp Eye Res. 1973 Nov 25;17(4):377-83 PMID: 4765260
  13. On the presence and mechanism of formation of heavy molecular weight aggregates in human normal and cataractous lenses.
    Exp Eye Res. 1973 Feb;15(2):185-92 PMID: 4692231
  14. The proportion of protein from the normal and cataractous human lens which exists as high molecular weight aggregates in vitro.
    Exp Eye Res. 1975 Jan;20(1):73-8 PMID: 1193192
  15. The concentration and localization of heavy molecular weight aggregates in aging normal and cataractous human lenses.
    Exp Eye Res. 1975 Apr;20(4):367-9 PMID: 1126401
  16. Color and solubility of the proteins of human cataracts.
    Invest Ophthalmol. 1968 Dec;7(6):634-50 PMID: 5727811
Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1979-11-01
Pages
1098-107
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2185697
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com