Literature DB >> 20553008

Increase in surface hydrophobicity of the cataract-associated P23T mutant of human gammaD-crystallin is responsible for its dramatically lower, retrograde solubility.

Ajay Pande1, Kalyan S Ghosh, Priya R Banerjee, Jayanti Pande.   

Abstract

The cataract-associated Pro23 to Thr (P23T) mutation in human gammaD-crystallin (HGD) has a variety of phenotypes and is geographically widespread. Therefore, there is considerable interest in understanding the molecular basis of cataract formation due to this mutation. We showed earlier [Pande, A., et al. (2005) Biochemistry 44, 2491-2500] that the probable basis of opacity in this case is the severely compromised, retrograde solubility and aggregation of P23T relative to HGD. The dramatic solubility change occurs even as the structure of the mutant protein remains essentially unchanged in vitro. We proposed that the retrograde solubility and aggregation of P23T were mediated by net hydrophobic, protein-protein interactions. On the basis of these initial findings for P23T and related mutants, and the subsequent finding that they show atypical phase behavior [McManus, J. J., et al. (2007) Proc. Natl. Acad. Sci. U.S.A. 104, 16856-16861], we concluded that the protein clusters formed in solutions of the mutant proteins were held together by net hydrophobic, anisotropic interactions. Here we show, using chemical probes, that the surface hydrophobicities of these mutants are inversely related to their solubility. Furthermore, by probing the isolated N-terminal domains of HGD and P23T directly, we find that the increase in the surface hydrophobicity of P23T is localized in the N-terminal domain. Modeling studies suggest the presence of sticky patches on the surface of the N-terminal domain that could be engaged in the formation of protein clusters via hydrophobic protein-protein interactions. This work thus provides direct evidence of the dominant role played by net hydrophobic and anisotropic protein-protein interactions in the aggregation of P23T.

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Year:  2010        PMID: 20553008      PMCID: PMC2913551          DOI: 10.1021/bi100664s

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


  28 in total

1.  Novel mutations in the gamma-crystallin genes cause autosomal dominant congenital cataracts.

Authors:  S T Santhiya; M Shyam Manohar; D Rawlley; P Vijayalakshmi; P Namperumalsamy; P M Gopinath; J Löster; J Graw
Journal:  J Med Genet       Date:  2002-05       Impact factor: 6.318

2.  Structure and thermodynamics of colloidal protein cluster formation: comparison of square-well and simple dipolar models.

Authors:  Teresa M Young; Christopher J Roberts
Journal:  J Chem Phys       Date:  2009-09-28       Impact factor: 3.488

3.  Molecular basis of a progressive juvenile-onset hereditary cataract.

Authors:  A Pande; J Pande; N Asherie; A Lomakin; O Ogun; J A King; N H Lubsen; D Walton; G B Benedek
Journal:  Proc Natl Acad Sci U S A       Date:  2000-02-29       Impact factor: 11.205

4.  Gamma-D crystallin gene (CRYGD) mutation causes autosomal dominant congenital cerulean cataracts.

Authors:  E Nandrot; C Slingsby; A Basak; M Cherif-Chefchaouni; B Benazzouz; Y Hajaji; S Boutayeb; O Gribouval; L Arbogast; A Berraho; M Abitbol; L Hilal
Journal:  J Med Genet       Date:  2003-04       Impact factor: 6.318

5.  Dimer formation from 1-amino-8-naphthalenesulfonate catalyzed by bovine serum albumin. A new fluorescent molecule with exceptional binding properties.

Authors:  C G Rosen; G Weber
Journal:  Biochemistry       Date:  1969-10       Impact factor: 3.162

6.  High-resolution X-ray crystal structures of human gammaD crystallin (1.25 A) and the R58H mutant (1.15 A) associated with aculeiform cataract.

Authors:  Ajit Basak; Orval Bateman; Christine Slingsby; Ajay Pande; Neer Asherie; Olutayo Ogun; George B Benedek; Jayanti Pande
Journal:  J Mol Biol       Date:  2003-05-16       Impact factor: 5.469

7.  The P23T cataract mutation causes loss of solubility of folded gammaD-crystallin.

Authors:  P Evans; K Wyatt; G J Wistow; O A Bateman; B A Wallace; C Slingsby
Journal:  J Mol Biol       Date:  2004-10-15       Impact factor: 5.469

8.  Special fasciculiform cataract caused by a mutation in the gammaD-crystallin gene.

Authors:  Xingchao Shentu; Ke Yao; Wen Xu; Shu Zheng; Songnian Hu; Xiaohua Gong
Journal:  Mol Vis       Date:  2004-03-29       Impact factor: 2.367

9.  A missense mutation in the gammaD crystallin gene (CRYGD) associated with autosomal dominant "coral-like" cataract linked to chromosome 2q.

Authors:  Donna S Mackay; Usha P Andley; Alan Shiels
Journal:  Mol Vis       Date:  2004-03-17       Impact factor: 2.367

10.  Autosomal dominant coralliform cataract related to a missense mutation of the gammaD-crystallin gene.

Authors:  Wei-zhen Xu; Shu Zheng; Shi-jie Xu; Wei Huang; Ke Yao; Su-zhan Zhang
Journal:  Chin Med J (Engl)       Date:  2004-05       Impact factor: 2.628

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  24 in total

1.  Blind attraction: the mechanism of an inherited congenital cataract.

Authors:  Neer Asherie
Journal:  Proc Natl Acad Sci U S A       Date:  2010-12-28       Impact factor: 11.205

2.  Cataract-linked γD-crystallin mutants have weak affinity to lens chaperones α-crystallins.

Authors:  Sanjay Mishra; Richard A Stein; Hassane S McHaourab
Journal:  FEBS Lett       Date:  2012-01-28       Impact factor: 4.124

3.  Increased hydrophobicity and decreased backbone flexibility explain the lower solubility of a cataract-linked mutant of γD-crystallin.

Authors:  Priya R Banerjee; Shadakshara S Puttamadappa; Ajay Pande; Alexander Shekhtman; Jayanti Pande
Journal:  J Mol Biol       Date:  2011-07-30       Impact factor: 5.469

4.  Temperature-Dependent Interactions Explain Normal and Inverted Solubility in a γD-Crystallin Mutant.

Authors:  Amir R Khan; Susan James; Michelle K Quinn; Irem Altan; Patrick Charbonneau; Jennifer J McManus
Journal:  Biophys J       Date:  2019-07-19       Impact factor: 4.033

5.  Structural and biochemical characterization of the childhood cataract-associated R76S mutant of human γD-crystallin.

Authors:  Fangling Ji; Jinwon Jung; Angela M Gronenborn
Journal:  Biochemistry       Date:  2012-03-14       Impact factor: 3.162

6.  Cataract-associated mutant E107A of human gammaD-crystallin shows increased attraction to alpha-crystallin and enhanced light scattering.

Authors:  Priya R Banerjee; Ajay Pande; Julita Patrosz; George M Thurston; Jayanti Pande
Journal:  Proc Natl Acad Sci U S A       Date:  2010-12-20       Impact factor: 11.205

7.  The cataract-associated V41M mutant of human γS-crystallin shows specific structural changes that directly enhance local surface hydrophobicity.

Authors:  Somireddy Venkata Bharat; Alexander Shekhtman; Jayanti Pande
Journal:  Biochem Biophys Res Commun       Date:  2013-11-25       Impact factor: 3.575

8.  Crystal structure of the cataract-causing P23T γD-crystallin mutant.

Authors:  Fangling Ji; Leonardus M I Koharudin; Jinwon Jung; Angela M Gronenborn
Journal:  Proteins       Date:  2013-06-17

9.  Aggregation of Trp > Glu point mutants of human gamma-D crystallin provides a model for hereditary or UV-induced cataract.

Authors:  Eugene Serebryany; Takumi Takata; Erika Erickson; Nathaniel Schafheimer; Yongting Wang; Jonathan A King
Journal:  Protein Sci       Date:  2016-04-18       Impact factor: 6.725

Review 10.  Mutations and mechanisms in congenital and age-related cataracts.

Authors:  Alan Shiels; J Fielding Hejtmancik
Journal:  Exp Eye Res       Date:  2016-06-19       Impact factor: 3.467

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