Conformational changes induced in lens α- and γ-crystallins by modification with glucose 6-phosphate. Implications for cataract
- 15 September 1987
- journal article
- research article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 246 (3) , 761-769
- https://doi.org/10.1042/bj2460761
Abstract
There is good evidence that the non-enzymic chemical modification of proteins plays a role in the aetiology of cataract and diabetic sequelae. This paper presents new evidence that glycosylation of two major lens structural crystallins, alpha- and gamma-crystallins, by glucose 6-phosphate (G6P) induces conformational changes in the proteins. In addition the surface charge on the molecules is altered. These changes would affect protein-protein and protein-water interactions within the lens and could lead to disruption of the short-range order of the lens proteins which is essential for lens transparency. Conformational changes to lens proteins are known to occur in human cataractous lenses but their cause in vivo is not established. Cumulative chemical modification of proteins, over a period of decades, is a strong candidate as a causal agent.This publication has 39 references indexed in Scilit:
- Homology between the primary structures of the major bovine β‐crystallin chainsEuropean Journal of Biochemistry, 1984
- Glucosylation of Low-Density Lipoproteins to an Extent Comparable to That Seen in Diabetes Slows Their CatabolismDiabetes, 1984
- Detection of nonenzymatic browning products in the human lensBiochimica et Biophysica Acta (BBA) - General Subjects, 1983
- X-ray analysis of the eye lens protein γ-II crystallin at 1·9 Å resolutionJournal of Molecular Biology, 1983
- Increased glycosylation of proteins from cataractous lenses in diabetesDiabetologia, 1983
- The principal site of nonenzymatic glycosylation of human serum albumin in vivo.Journal of Biological Chemistry, 1983
- Short-range order of crystallin proteins accounts for eye lens transparencyNature, 1983
- The nucleotide sequence of a cloned cDNA corresponding to one of the γ‐crystallins from the eye lens of the frog Rana temporariaFEBS Letters, 1982
- Spectroscopic investigations of bovine lens crystallins. 1. Circular dichroism and intrinsic fluorescenceBiochemistry, 1982
- N-terminal groups of lens proteinsExperimental Eye Research, 1968