Literature DB >> 16699822

Age-related changes of alpha-crystallin aggregate in human lens.

N Fujii1, Y Shimmyo, M Sakai, Y Sadakane, T Nakamura, Y Morimoto, T Kinouchi, Y Goto, K Lampi.   

Abstract

Lens alpha-crystallin, composed of two subunits alpha A- and alpha B-crystallin, forms large aggregates in the lens of the eye. The present study investigated the aggregate of human lens alpha-crystallin from elderly and young donors. Recombinant alpha A- and alpha B-crystallins in molar ratios of alpha A to alpha B at 1:1, corresponding to the aged sample, were also studied in detail. We found by ultra-centrifugation analysis that the alpha-crystallin aggregate from elderly donors was large and heterogeneous with an average sedimentation coefficient of 30 S and a range of 20-60 S at 37 degrees C. This was higher compared to the young samples that had an average sedimentation coefficient of 17 S. The sedimentation coefficients of recombinant alpha A- and alpha B-crystallins were approximately 12 S and 15 S, respectively. Even when recombinant alpha-crystallins were mixed in molar ratios equivalent to those found in vivo, similar S values as the native aged alpha-crystallin aggregates were not obtained. Changes in the self-association of alpha-crystallin aggregate were correlated to changes in chaperone activity. Alpha-crystallin from young donors, and recombinant alpha A- and alpha B-crystallin and their mixtures showed chaperone activity, which was markedly lost in samples from the aged alpha-crystallin aggregates.

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Year:  2006        PMID: 16699822     DOI: 10.1007/s00726-006-0303-4

Source DB:  PubMed          Journal:  Amino Acids        ISSN: 0939-4451            Impact factor:   3.520


  15 in total

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Journal:  Mol Vis       Date:  2009-12-19       Impact factor: 2.367

2.  Identification of histidine residues involved in Zn(2+) binding to αA- and αB-crystallin by chemical modification and MALDI TOF mass spectrometry.

Authors:  Srabani Karmakar; K P Das
Journal:  Protein J       Date:  2012-10       Impact factor: 2.371

3.  Covalent structural changes in unfolded GroES that lead to amyloid fibril formation detected by NMR: insight into intrinsically disordered proteins.

Authors:  Hisanori Iwasa; Shunsuke Meshitsuka; Kunihiro Hongo; Tomohiro Mizobata; Yasushi Kawata
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4.  A rapid, comprehensive liquid chromatography-mass spectrometry (LC-MS)-based survey of the Asp isomers in crystallins from human cataract lenses.

Authors:  Norihiko Fujii; Hiroaki Sakaue; Hiroshi Sasaki; Noriko Fujii
Journal:  J Biol Chem       Date:  2012-09-24       Impact factor: 5.157

5.  Impact of diabetes on alpha-crystallins and other heat shock proteins in the eye.

Authors:  Erich A Heise; Patrice E Fort
Journal:  J Ocul Biol Dis Infor       Date:  2011-12-23

6.  αA-crystallin peptide SDRDKFVIFLDVKHF accumulating in aging lens impairs the function of α-crystallin and induces lens protein aggregation.

Authors:  Puttur Santhoshkumar; Murugesan Raju; K Krishna Sharma
Journal:  PLoS One       Date:  2011-04-28       Impact factor: 3.240

7.  Characterization of an antibody that recognizes peptides containing D-β-aspartyl residues.

Authors:  Kenzo Aki; Norihiko Fujii; Takeshi Saito; Noriko Fujii
Journal:  Mol Vis       Date:  2012-04-21       Impact factor: 2.367

8.  Structural features of isomerizable aspartyl residues in human α-crystallins.

Authors:  Ken-ichi Shimizu; Akiko Kita; Noriko Fujii; Kunio Miki
Journal:  Mol Vis       Date:  2012-07-04       Impact factor: 2.367

9.  Racemization in cataractous lens from diabetic and aging individuals: analysis of Asp 58 residue in αA-crystallin.

Authors:  Xiang-Jia Zhu; Ke-Ke Zhang; Wen-Wen He; Jiao Qi; Yi Lu
Journal:  Aging (Albany NY)       Date:  2021-06-07       Impact factor: 5.682

10.  Kinetics of isomerization and inversion of aspartate 58 of αA-crystallin peptide mimics under physiological conditions.

Authors:  Kenzo Aki; Norihiko Fujii; Noriko Fujii
Journal:  PLoS One       Date:  2013-03-07       Impact factor: 3.240

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