Age-dependent association of γ-crystallins with aged α-crystallins from old bovine lens

被引:0
|
作者
Takemoto, Larry [1 ]
Ponce, Aldo [1 ]
Sorenson, Christopher M. [2 ]
机构
[1] Kansas State Univ, Div Biol, Manhattan, KS 66506 USA
[2] Kansas State Univ, Dept Phys, Manhattan, KS 66506 USA
来源
MOLECULAR VISION | 2008年 / 14卷 / 112-15期
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中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Purpose: Previous theoretical and experimental studies have predicted that the loss of weak protein interactions between alpha- and gamma-crystallins could result in a decrease in the transparent properties of the aging lens. Methods: alpha-Crystallins were prepared from the nucleus of old bovine lens, and gamma-crystallins were prepared from whole fetal bovine lens or from the nucleus of old bovine lens. The possible interactions of old alpha-crystallins with either old gamma-crystallins or fetal gamma-crystallins were quantitated at equilibrium using microequilibrium dialysis. The amount of each gamma-crystallin species in the "full" versus "empty" chambers was determined by reverse phase chromatography to obtain a binding ratio (full/empty). Results: A binding ratio greater than 1.00 is indicative of a alpha-crystallin/gamma-crystallin interaction. Within experimental error (+/- 2X standard deviation), there were no interactions between aged gamma-crystallins with aged alpha-crystallins while there were significant interactions between some of the fetal gamma-crystallins with aged a-crystallins. Conclusions: In the aged bovine lens, when transparency is known to decrease, there is no detectable interaction of gamma-crystallins with alpha-crystallins as measured by microequilibrium dialysis. The results are consistent with the hypothesis that short-range, weak, attractive interactions between alpha- and gamma-crystallins are necessary for maximum transparency of the lens.
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页码:970 / 974
页数:5
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