Journal
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
Volume 1832, Issue 2, Pages 302-311Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.bbadis.2012.11.005
Keywords
beta B1-crystallin; Inherited mutation; Congenital cataract-microcornea syndrome; Molecular dynamic simulation; Protein aggregation; Limited proteolysis
Funding
- National Key Basic Research and Development (973) Program of China [2010CB912402]
- National Natural Science Foundation of China [30970559]
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Congenital hereditary cataract, which is mainly caused by the deposition of crystallins in light-scattering particles, is one of the leading causes of newborn blindness in human beings. Recently, an autosomal dominant congenital cataract-microcornea syndrome in a Chinese family has been associated with the S129R mutation in beta B1-crystallin. To investigate the underlying molecular mechanism, we examined the effect of the mutation on beta B1-crystallin structure and thermal stability. Biophysical experiments indicated that the mutation impaired the oligomerization of beta B1-crystallin and shifted the dimer-monomer equilibrium to monomer. Molecular dynamic simulations revealed that the mutation altered the hydrogen-bonding network and hydrophobic interactions in the subunit interface of the dimeric protein, which resulted in the opening of the tightly associated interacting sites to allow the infiltration of the solvent molecules into the interface. Despite the disruption of beta B1-crystallin assembly, the thermal stability of beta B1-crystallin was increased by the mutation accompanied by the reduction of thermal aggregation at high temperatures. Further analysis indicated that the mutation significantly increased the sensitivity of beta B1-crystallin to trypsin hydrolysis. The digested fragments of the mutant were prone to aggregate and unable to protect beta B1-crystallin against aggregation. These results indicated that the thermal stability-beneficial mutation S129R in beta B1-crystallin provided an excellent model for discovering molecular mechanisms apart from solubility and stability. Our results also highlighted that the increased sensitivity of mutated crystallins towards proteases might play a crucial role in the pathogenesis of congenital hereditary cataract and associated syndrome. (C) 2012 Elsevier B.V. All rights reserved.
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