Literature DB >> 20836128

Importance of eye lens α-crystallin heteropolymer with 3:1 αA to αB ratio: stability, aggregation, and modifications.

Pasumarthi Srinivas1, Akkaladevi Narahari, J Mark Petrash, Musti J Swamy, Geereddy Bhanuprakash Reddy.   

Abstract

Chaperone-like activity (CLA) of α-crystallin is essential not only for the maintenance of eye lens transparency but also in the biology of other tissues. Eye lens α-crystallin is a heteropolymer composed of two homologous subunits, αA and αB, and in most vertebrates they are present in a ratio of 3:1. The structural and functional significance of this specific ratio of α-crystallin subunits is of considerable interest in understanding its role in the eye lens transparency. Previously, we have shown that although at physiologically relevant conditions αB-crystallin has greater CLA, under stress conditions such as elevated temperatures α-crystallin heteropolymer with 3:1 αA to αB ratio displayed higher CLA (Srinivas et al., Biochem. J., 2008, 414, 453 - 460). Herein, we provide a rationale for the existence of α-crystallin heteropolymer with 3:1 αA to αB ratio in terms of structural stability, aggregation pattern, and susceptibility to posttranslational modifications that could explain the importance of the heteropolymer of α-crystallin in the eye lens. We demonstrate that αA-crystallin is not only more stable but also imparts stability to the heteropolymer by preventing the aggregation of αB-crystallin at higher temperatures by using differential scanning calorimetry, size-exclusion chromatography, and denaturant-induced unfolding methods. Further, the physiological significance of heteropolymer with higher proportion of αA subunit is substantiated by using a heteropolymer with mutant (F71L) αA-crystallin and the susceptibility of 3:1 heteropolymer to glycation-induced modifications. Thus, the existence of 3:1 heteropolymer might be vital for the eye lens transparency under diverse conditions to prevent cataract.
© 2010 IUBMB IUBMB Life.

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Year:  2010        PMID: 20836128      PMCID: PMC3615983          DOI: 10.1002/iub.373

Source DB:  PubMed          Journal:  IUBMB Life        ISSN: 1521-6543            Impact factor:   3.885


  43 in total

1.  Lens alpha-crystallin: function and structure.

Authors:  J Horwitz; M P Bova; L L Ding; D A Haley; P L Stewart
Journal:  Eye (Lond)       Date:  1999-06       Impact factor: 3.775

2.  The molecular chaperone alpha-crystallin is in kinetic competition with aggregation to stabilize a monomeric molten-globule form of alpha-lactalbumin.

Authors:  R A Lindner; T M Treweek; J A Carver
Journal:  Biochem J       Date:  2001-02-15       Impact factor: 3.857

Review 3.  Alpha-crystallin.

Authors:  Joseph Horwitz
Journal:  Exp Eye Res       Date:  2003-02       Impact factor: 3.467

4.  Cloning and characterization of a thermostable catfish alphaB-crystallin with chaperone-like activity at high temperatures.

Authors:  Chung-Ming Yu; Gu-Gang Chang; Hui-Chuan Chang; Shyh-Horng Chiou
Journal:  Exp Eye Res       Date:  2004-08       Impact factor: 3.467

5.  Heat-induced conformational change of human lens recombinant alphaA- and alphaB-crystallins.

Authors:  J J Liang; T X Sun; N J Akhtar
Journal:  Mol Vis       Date:  2000-03-02       Impact factor: 2.367

Review 6.  Crystallins, genes and cataract.

Authors:  Suraj P Bhat
Journal:  Prog Drug Res       Date:  2003

7.  AlphaB-crystallin in lens development and muscle integrity: a gene knockout approach.

Authors:  J P Brady; D L Garland; D E Green; E R Tamm; F J Giblin; E F Wawrousek
Journal:  Invest Ophthalmol Vis Sci       Date:  2001-11       Impact factor: 4.799

8.  Thermodynamic stability of human lens recombinant alphaA- and alphaB-crystallins.

Authors:  T X Sun; N J Akhtar; J J Liang
Journal:  J Biol Chem       Date:  1999-11-26       Impact factor: 5.157

9.  Temperature-dependent chaperone activity and structural properties of human alphaA- and alphaB-crystallins.

Authors:  G B Reddy; K P Das; J M Petrash; W K Surewicz
Journal:  J Biol Chem       Date:  2000-02-18       Impact factor: 5.157

10.  Differential protective activity of alpha A- and alphaB-crystallin in lens epithelial cells.

Authors:  U P Andley; Z Song; E F Wawrousek; T P Fleming; S Bassnett
Journal:  J Biol Chem       Date:  2000-11-24       Impact factor: 5.157

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  14 in total

1.  Differences in α-Crystallin isomerization reveal the activity of protein isoaspartyl methyltransferase (PIMT) in the nucleus and cortex of human lenses.

Authors:  Yana A Lyon; Georgette M Sabbah; Ryan R Julian
Journal:  Exp Eye Res       Date:  2018-03-20       Impact factor: 3.467

Review 2.  The multifaceted nature of αB-crystallin.

Authors:  Junna Hayashi; John A Carver
Journal:  Cell Stress Chaperones       Date:  2020-05-07       Impact factor: 3.667

3.  Binding of γ-crystallin substrate prevents the binding of copper and zinc ions to the molecular chaperone α-crystallin.

Authors:  Kalyan S Ghosh; Ajay Pande; Jayanti Pande
Journal:  Biochemistry       Date:  2011-03-30       Impact factor: 3.162

4.  Temperature-dependent structural and functional properties of a mutant (F71L) αA-crystallin: molecular basis for early onset of age-related cataract.

Authors:  Vakdevi Validandi; V Sudhakar Reddy; P N B S Srinivas; Niklaus H Mueller; S G Bhagyalaxmi; T Padma; J Mark Petrash; G Bhanuprakash Reddy
Journal:  FEBS Lett       Date:  2011-11-11       Impact factor: 4.124

5.  Alpha-Crystallin Association with the Model of Human and Animal Eye Lens-Lipid Membranes is Modulated by Surface Hydrophobicity of Membranes.

Authors:  Raju Timsina; Geraline Trossi-Torres; Jackson Thieme; Matthew O'Dell; Nawal K Khadka; Laxman Mainali
Journal:  Curr Eye Res       Date:  2022-03-22       Impact factor: 2.555

6.  RNA aptamers targeted for human αA-crystallin do not bind αB-crystallin, and spare the α-crystallin domain.

Authors:  Prabhat K Mallik; Hua Shi; Jayanti Pande
Journal:  Biochem Biophys Res Commun       Date:  2017-07-15       Impact factor: 3.575

7.  Aggregation and fibrillation of eye lens crystallins by homocysteinylation; implication in the eye pathological disorders.

Authors:  Sima Khazaei; Reza Yousefi; Mohammad-Mehdi Alavian-Mehr
Journal:  Protein J       Date:  2012-12       Impact factor: 2.371

8.  Interaction of Alpha-Crystallin with Phospholipid Membranes.

Authors:  Laxman Mainali; William J O'Brien; Raju Timsina
Journal:  Curr Eye Res       Date:  2020-07-12       Impact factor: 2.424

9.  Interaction of alpha-crystallin with four major phospholipids of eye lens membranes.

Authors:  Raju Timsina; Nawal K Khadka; David Maldonado; Laxman Mainali
Journal:  Exp Eye Res       Date:  2020-10-27       Impact factor: 3.467

Review 10.  Association of Alpha-Crystallin with Fiber Cell Plasma Membrane of the Eye Lens Accompanied by Light Scattering and Cataract Formation.

Authors:  Raju Timsina; Laxman Mainali
Journal:  Membranes (Basel)       Date:  2021-06-15
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