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Reaction Pathways Initiated by One-electron Oxidation of Guanine: Reaction Pathways Leading to Stable End Products

8-hydroxyguanine (8-oxoG) is one of the most important products resulting from the oxidation of guanine in DNA. 8-oxoG is known as a biomarker of oxidative stress such as lung cancer. 2,5-diamino-4H-imidazol-4-one (Iz) and its hydrolysis product 2,2-diamino-4-[(2-deoxy-β-D-erythro-pentofuranosyl)-amino]-2,5-dihydrooxazol-5-one (Oz) are also important products of oxidation of guanine in DNA. Recently, novel types of dimer intermediates related to 8-oxoG and Iz have been identified in our research lab. Using high performance liquid chromatography (HPLC), LC-MS, and NMR coupled with educated hypotheses, it is possible to identify the products, X1 and X2, resulting from the oxidation of guanine and decipher the mechanisms leading to the products. Gaining a better understanding of these mechanisms could potentially lead to more effective medical treatment of conditions resulting from oxidative stress. X1 and X2 were isolated in large amounts from deoxyguanosine (dGuo) via photochemical oxidation. Subsequent testing included a comparison of the effects of different pH values as well as determination of the lifetimes for the X2 product during hydrolysis and reactions with amines. It was shown from the results that X1 undergoes further oxidation to produce X2.

Identiferoai:union.ndltd.org:ETSU/oai:dc.etsu.edu:honors-1805
Date01 May 2021
CreatorsCutright, Zach
PublisherDigital Commons @ East Tennessee State University
Source SetsEast Tennessee State University
Detected LanguageEnglish
Typetext
Formatapplication/pdf
SourceUndergraduate Honors Theses
RightsCopyright by the authors., http://creativecommons.org/licenses/by-nc-nd/3.0/

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