Pharmacological chaperone for α-crystallin partially restores transparency in cataract models

Author:

Makley Leah N.1,McMenimen Kathryn A.1,DeVree Brian T.2,Goldman Joshua W.3,McGlasson Brittney N.3,Rajagopal Ponni4,Dunyak Bryan M.1,McQuade Thomas J.5,Thompson Andrea D.1,Sunahara Roger2,Klevit Rachel E.4,Andley Usha P.3,Gestwicki Jason E.15

Affiliation:

1. Departments of Pathology, Biological Chemistry, and Medicinal Chemistry and the Life Sciences Institute, University of Michigan, Ann Arbor, MI, USA.

2. Department of Pharmacology, University of Michigan, Ann Arbor, MI, USA.

3. Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, MO, USA.

4. Department of Biochemistry, University of Washington, Seattle, WA, USA.

5. Center for Chemical Genomics, University of Michigan, Ann Arbor, MI, USA.

Abstract

A visionary approach to transparency Cataracts are the most common cause of vision loss, especially in our ever-increasing elderly population. Cataracts arise when crystallin, a major protein component of the eye lens, begins to aggregate, which causes the lens to become cloudy. Makley et al. explored whether small molecules that reverse this aggregation might have therapeutic potential for treating cataracts, which normally require surgery (see the Perspective by Quinlan). They used a screening method that monitors the effect of ligands on temperature-dependent protein unfolding and identified several compounds that bind and stabilize the soluble form of crystallin. In proof-of-concept studies, one of these compounds improved lens transparency in mice. Science , this issue p. 674 ; see also p. 636

Funder

NIH

American Foundation for Pharmaceutical Education

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference29 articles.

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4. Amyloid Fibril Formation by Lens Crystallin Proteins and Its Implications for Cataract Formation

5. Characterisation of Amyloid Fibril Formation by Small Heat-shock Chaperone Proteins Human αA-, αB- and R120G αB-Crystallins

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