Literature DB >> 9688580

Subunit exchange of lens alpha-crystallin: a fluorescence energy transfer study with the fluorescent labeled alphaA-crystallin mutant W9F as a probe.

T X Sun1, N J Akhtar, J J Liang.   

Abstract

A Trp-free alphaA-crystallin mutant (W9F) was prepared by site-directed mutation. This mutant appears to be identical to the wild-type in terms of conformation (secondary and tertiary structures). W9F was labeled with a sulfhydryl-specific fluorescent probe, 2-(4'-maleimidylanilino) naphthalene-6-sulfonate (MIANS), and used in a subunit exchange between alphaA- and alphaA-crystallins as well as between alphaA- and alphaB-crystallins, studied by measurement of fluorescence resonance energy transfer. Energy transfer was observed between Trp (donor, with emission maximum at 336 nm) of wild-type alphaA- or alphaB-crystallin and MIANS (acceptor, with absorption maximum at 313 nm) of labeled W9F when subunit exchange occurred. Time-dependent decrease of Trp and increase of MIANS fluorescence were recorded. The exchange was faster at 37 degrees C than at 25 degrees C. The energy transfer efficiency was greater between homogeneous subunits (alphaA-alphaA) than between heterogeneous subunits (alphaA-alphaB). A previous exchange study with isoelectric focusing indicated a complete but slow exchange between alphaA and alphaB subunits. The present study showed that the exchange was a fast process, and the different energy transfer efficiencies between alphaA-alphaA and alphaA-alphaB indicated that alphaA- and alphaB-crystallins were not necessarily structurally equivalent.

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Year:  1998        PMID: 9688580     DOI: 10.1016/s0014-5793(98)00707-8

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  9 in total

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Authors:  J J Liang; T X Sun; N J Akhtar
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3.  Fluorescence resonance energy transfer study of subunit exchange in human lens crystallins and congenital cataract crystallin mutants.

Authors:  Jack J Liang; Bing-Fen Liu
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4.  Cell penetration peptides for enhanced entry of αB-crystallin into lens cells.

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5.  Structural and functional changes in the alpha A-crystallin R116C mutant in hereditary cataracts.

Authors:  B A Cobb; J M Petrash
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6.  Interactions and chaperone function of alphaA-crystallin with T5P gammaC-crystallin mutant.

Authors:  Jack J-N Liang
Journal:  Protein Sci       Date:  2004-09       Impact factor: 6.725

7.  Chemical modulation of the chaperone function of human alphaA-crystallin.

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8.  AlphaA-crystallin R49Cneo mutation influences the architecture of lens fiber cell membranes and causes posterior and nuclear cataracts in mice.

Authors:  Usha P Andley
Journal:  BMC Ophthalmol       Date:  2009-07-20       Impact factor: 2.209

9.  Confocal fluorescence resonance energy transfer microscopy study of protein-protein interactions of lens crystallins in living cells.

Authors:  Bing-Fen Liu; Kumarasamy Anbarasu; Jack J-N Liang
Journal:  Mol Vis       Date:  2007-06-14       Impact factor: 2.367

  9 in total

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