August 1998
Volume 39, Issue 9
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Articles  |   August 1998
Aggregation in aqueous solutions of bovine lens gamma-crystallins: special role of gamma(s).
Author Affiliations
  • C Liu
    Department of Physics and Center for Materials Sciences and Engineering, Massachusetts Institute of Technology, Cambridge 02139, USA.
  • J Pande
    Department of Physics and Center for Materials Sciences and Engineering, Massachusetts Institute of Technology, Cambridge 02139, USA.
  • A Lomakin
    Department of Physics and Center for Materials Sciences and Engineering, Massachusetts Institute of Technology, Cambridge 02139, USA.
  • O Ogun
    Department of Physics and Center for Materials Sciences and Engineering, Massachusetts Institute of Technology, Cambridge 02139, USA.
  • G B Benedek
    Department of Physics and Center for Materials Sciences and Engineering, Massachusetts Institute of Technology, Cambridge 02139, USA.
Investigative Ophthalmology & Visual Science August 1998, Vol.39, 1609-1619. doi:
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      C Liu, J Pande, A Lomakin, O Ogun, G B Benedek; Aggregation in aqueous solutions of bovine lens gamma-crystallins: special role of gamma(s).. Invest. Ophthalmol. Vis. Sci. 1998;39(9):1609-1619.

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Abstract

PURPOSE: To study the aggregation of bovine gamma-crystallins in aqueous solutions and the effect of gamma(s)-crystallin on the aggregation of other gamma-crystallins. METHODS: Aggregation in aqueous solutions of gamma(s)-, gammaII-, and gammaIVa-crystallin was monitored by quasielastic light scattering. Aggregation in mixtures of gamma(s)- and gammaII-crystallin, and gamma(s)- and gammaIVa-crystallin, was also monitored by light scattering. RESULTS: All of the gamma-crystallins studied formed large aggregates (or "megamers") in aqueous solutions. However, each protein differed in the relative rates of formation of megamers. Gamma(s)-crystallin formed megamers much more slowly than gammaII- and gammaIVa-crystallin. In solutions containing mixtures of gammaII and gamma(s), and gammaIVa and gamma(s), gamma(s)-crystallin significantly suppressed the aggregation of gammaII- and gammaIVa-crystallin. Megamerization seemed to be associated with thiol oxidation in these proteins. CONCLUSIONS: Gamma-crystallins undergo aggregation in which a small fraction of the proteins form a few large aggregates, whereas the larger proportion of the proteins remain monomeric. This suggests that the megamerization is preceded by an initial modification of the protein. The modification is associated with the thiol groups, and only such modified protein species participate in megamerization. The presence of gamma(s) significantly slows the megamerization of gammaII- and gammaIVa-crystallin. This fact, together with the previous finding that gamma(s) strongly reduces the phase separation temperatures of the gamma-crystallins, suggests that gamma(s)-crystallin plays an important role in suppressing the formation of light-scattering elements and helps maintain lens transparency.

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