共 116 条
Protein misfolding and aggregation in cataract disease and prospects for prevention
被引:342
作者:

Moreau, Kate L.
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机构:
MIT, Dept Biol, Cambridge, MA 02139 USA MIT, Dept Biol, Cambridge, MA 02139 USA

King, Jonathan A.
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h-index: 0
机构:
MIT, Dept Biol, Cambridge, MA 02139 USA MIT, Dept Biol, Cambridge, MA 02139 USA
机构:
[1] MIT, Dept Biol, Cambridge, MA 02139 USA
关键词:
GAMMA-D-CRYSTALLIN;
AGE-RELATED-CHANGES;
AMYLOID FIBRIL FORMATION;
OXIDIZED BETA-B3-CRYSTALLIN PEPTIDE;
SELENITE-INDUCED CATARACTOGENESIS;
ALPHA-B-CRYSTALLIN;
HUMAN LENS;
IN-VITRO;
C-CRYSTALLIN;
MASS-SPECTROMETRY;
D O I:
10.1016/j.molmed.2012.03.005
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:
The transparency of the eye lens depends on maintaining the native tertiary structures and solubility of the lens crystallin proteins over a lifetime. Cataract, the leading cause of blindness worldwide, is caused by protein aggregation within the protected lens environment. With age, covalent protein damage accumulates through pathways thought to include UV radiation, oxidation, deamidation, and truncations. Experiments suggest that the resulting protein destabilization leads to partially unfolded, aggregation-prone intermediates and the formation of insoluble, light-scattering protein aggregates. These aggregates either include or overwhelm the protein chaperone content of the lens. Here, we review the causes of cataract and nonsurgical methods being investigated to inhibit or delay cataract development, including natural product-based therapies, modulators of oxidation, and protein aggregation inhibitors.
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页码:273 / 282
页数:10
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