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Next generation, 'Standards-Free' Metabolite Identification Pipeline

$190,103R03FY2017CANIH

Battelle Pacific Northwest Laboratories, Richland WA

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Linked publications & trials

Abstract

Research Plan Abstract The capability to chemically identify thousands of metabolites and other chemicals in clinical samples will revolutionize the search for environmental, dietary, and metabolic determinants of disease. By comparison to near-comprehensive genetic information, comparatively little is understood of the totality of the human metabolome, largely due to insufficiencies in molecular identification methods. Through innovations in computational chemistry, we propose to overcome a significant, long standing obstacle in the field of metabolomics: the absence of methods for accurate and comprehensive identification of small molecules without relying on data from analysis of authentic chemical standards. A paradigm shift in metabolomics, we will use a gas-phase molecular property, collision cross section, that can be both accurately predicted computationally and consistently measured experimentally, and which can thus be used for comprehensive identification of the metabolome without the need for authentic chemical standards. The outcomes of this proposal directly advance the mission and goals of the NIH Common Fund by: (i) transforming metabolomics science by enabling consideration of the totality of the human metabolome through optimized identification of currently unidentifiable molecules, eventually reaching hundreds of thousands of molecules, and (ii) developing standardized computational tools to increase the national capacity for biomedical researchers to identify metabolites quickly and accurately. This work is significant because it enables comprehensive and confident chemical measurement of the metabolome. This work is innovative because it utilizes a high throughput, high accuracy, quantum-chemistry-based computational and chemical informatics platform to predict physical-chemical properties of metabolites from first principles.

View original record on NIH RePORTER →