Age-dependent association of γ-crystallins with aged α-crystallins from old bovine lens
被引:0
作者:
Takemoto, Larry
论文数: 0引用数: 0
h-index: 0
机构:
Kansas State Univ, Div Biol, Manhattan, KS 66506 USAKansas State Univ, Div Biol, Manhattan, KS 66506 USA
Takemoto, Larry
[1
]
Ponce, Aldo
论文数: 0引用数: 0
h-index: 0
机构:
Kansas State Univ, Div Biol, Manhattan, KS 66506 USAKansas State Univ, Div Biol, Manhattan, KS 66506 USA
Ponce, Aldo
[1
]
Sorenson, Christopher M.
论文数: 0引用数: 0
h-index: 0
机构:
Kansas State Univ, Dept Phys, Manhattan, KS 66506 USAKansas State Univ, Div Biol, Manhattan, KS 66506 USA
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
关键词:
D O I:
暂无
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.