Bioactivity Profiling with Parallel Mass Spectrometry Reveals an Assemblage of Green Tea Metabolites Affording Protection against Human Huntingtin and α-Synuclein Toxicity

Russell B. Williams, Will R. Gutekunst, P. Matthew Joyner, Wenzhen Duan, Qing Li, Christopher A. Ross, Todd D. Williams§ and Robert H. Cichewicz*
Natural Products Discovery Group, Department of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma 73019, Division of Neurobiology, Department of Psychiatry, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287, and Mass Spectrometry Lab, University of Kansas, Lawrence, Kansas 66045
J. Agric. Food Chem., 2007, 55 (23), pp 9450–9456
DOI: 10.1021/jf072241x
Publication Date (Web): October 19, 2007
Copyright © 2007 American Chemical Society

University of Oklahoma.

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Johns Hopkins University School of Medicine.

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University of Kansas.

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* To whom correspondence should be addressed. Telephone: (405) 325-6969 . Fax: (405) 325-6111. E-mail: rhcichewicz@ou.edu.

Abstract

Abstract Image

Aberrant protein aggregation and misfolding are key pathological features of many neurodegenerative disorders, including Huntington’s and Parkinson’s diseases. Compounds that offer protection from toxicity associated with aggregation-prone neurodegenerative proteins may have applications for the treatment of a multitude of disorders. A high-throughput bioassay system with parallel electrospray ionization mass spectrometry screening has been designed for critical evaluation of milligram quantities of natural product extracts, including dietary substances, for compounds of pharmacological relevance to the treatment of human neurodegenerative diseases. Using Saccharomyces cerevisiae strains engineered to express mutant human huntingtin and α-synuclein, we are able to identify extracts and compounds that protect cells from toxicity associated with these proteins. Applying this screening paradigm, we determined that a bioactive green tea extract contains an assemblage of catechins that were individually characterized for their respective protective effects against huntingtin and α-synuclein toxicity.

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History

  • Published In Issue November 14, 2007
  • Article ASAPOctober 19, 2007
  • Received: July 25, 2007
    Accepted: September 14, 2007
    Revised: September 13, 2007

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