Literature DB >> 17279772

Cleavage of the C-terminal serine of human alphaA-crystallin produces alphaA1-172 with increased chaperone activity and oligomeric size.

Atya Aziz1, Puttur Santhoshkumar, Krishna K Sharma, Edathara C Abraham.   

Abstract

This study aimed to study the oligomeric size, structure, hydrodynamic properties, and chaperone function of the C-terminally truncated human alphaA-crystallin mutants with special emphasis on alphaA1-172 which is the cleavage product of the Ser172-Ser173 bond, unique to human lenses and constituting a major part of alphaA-crystallin. Various truncated forms of human alphaA-crystallins were prepared by site-directed mutagenesis. The proteins were expressed in Escherichia coli BL21(DE3) pLysS cells and purified by size exclusion column chromatography. Molecular masses and the other hydrodynamic properties were determined by dynamic light scattering measurements. The secondary and tertiary structural changes were assessed by far- and near-UV CD spectra measurements, respectively. Chaperone activity was determined by using ADH, insulin, and betaL-crystallin as the target proteins. alphaAlpha1-172 exhibited a significant increase in oligomeric size, i.e., 866 kDa by light scattering measurements as compared to 702 kDa in alphaA-wt. alphaAlpha1-172 and alphaA-wt had similar secondary structure, but the former exhibited slightly altered tertiary structure. The most interesting observation was that alphaAlpha1-172 behaved as a 28-46% better chaperone than alphaA-wt. The oligomeric size and structure of alphaAlpha1-168 were similar to those of alphaA-wt, while the chaperone activity was decreased by 12-23%. alphaAlpha1-162, on the other hand, had an oligomeric size of 400 kDa, a decrease in chaperone activity of 80-100%, and significantly altered secondary and tertiary structures. The data show that the overall chaperone function of alphaA-crystallin will be significantly improved by the presence of the major truncated product alphaAlpha1-172. This will be beneficial to the lens undergoing oxidative stress. Since alphaAlpha1-168 and alphaAlpha1-162 are present only in small amounts, their effect would be minimal.

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Year:  2007        PMID: 17279772     DOI: 10.1021/bi0618722

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  16 in total

Review 1.  Spatiotemporal changes in the human lens proteome: Critical insights into long-lived proteins.

Authors:  Kevin L Schey; Zhen Wang; Michael G Friedrich; Donita L Garland; Roger J W Truscott
Journal:  Prog Retin Eye Res       Date:  2019-11-06       Impact factor: 21.198

2.  Quaternary structural parameters of the congenital cataract causing mutants of αA-crystallin.

Authors:  Rajshekhar Kore; Rebecca A Hedges; Lalita Oonthonpan; Puttur Santhoshkumar; Krishna K Sharma; Edathara C Abraham
Journal:  Mol Cell Biochem       Date:  2011-11-02       Impact factor: 3.396

3.  Deletion of (54)FLRAPSWF(61) residues decreases the oligomeric size and enhances the chaperone function of alphaB-crystallin.

Authors:  Puttur Santhoshkumar; Raju Murugesan; K Krishna Sharma
Journal:  Biochemistry       Date:  2009-06-16       Impact factor: 3.162

4.  Age-related changes in the spatial distribution of human lens alpha-crystallin products by MALDI imaging mass spectrometry.

Authors:  Angus C Grey; Kevin L Schey
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-04-22       Impact factor: 4.799

5.  Reversal of chaperone activity loss of glycated alphaA-crystallin by a crosslink breaker.

Authors:  Poppy Datta; Latha Kallur; Edathara C Abraham
Journal:  Mol Cell Biochem       Date:  2008-06-03       Impact factor: 3.396

6.  C-Terminal truncation affects subunit exchange of human alphaA-crystallin with alphaB-crystallin.

Authors:  Latha S Kallur; Atya Aziz; Edathara C Abraham
Journal:  Mol Cell Biochem       Date:  2007-10-02       Impact factor: 3.396

Review 7.  Lens aging: effects of crystallins.

Authors:  K Krishna Sharma; Puttur Santhoshkumar
Journal:  Biochim Biophys Acta       Date:  2009-05-20

8.  Functional Rescue of Cataract-Causing αA-G98R-Crystallin by Targeted Compensatory Suppressor Mutations in Human αA-Crystallin.

Authors:  Ashutosh S Phadte; Sundararajan Mahalingam; Puttur Santhoshkumar; Krishna K Sharma
Journal:  Biochemistry       Date:  2019-09-20       Impact factor: 3.162

Review 9.  α-Crystallins in the Vertebrate Eye Lens: Complex Oligomers and Molecular Chaperones.

Authors:  Marc A Sprague-Piercy; Megan A Rocha; Ashley O Kwok; Rachel W Martin
Journal:  Annu Rev Phys Chem       Date:  2020-12-15       Impact factor: 12.703

10.  Structural and functional roles of deamidation of N146 and/or truncation of NH2- or COOH-termini in human αB-crystallin.

Authors:  C O Asomugha; R Gupta; O P Srivastava
Journal:  Mol Vis       Date:  2011-09-14       Impact factor: 2.367

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