Date of Graduation
Summer 2014
Degree
Master of Science in Chemistry
Department
Chemistry and Biochemistry
Committee Chair
Gary Meints
Abstract
Deoxyribonucleic acid (DNA) contains all the genetic information needed for life. It is important for the DNA integrity of the sequence and structure be maintained in order to interact properly with proteins. The purpose of this project is to determine if there are significant changes to DNA structure due to the lesion 3, N4-etheno-2'-deoxycytidine (εC). The DNA sequence I studied is [ds(5'-C-G-C-G-A-A-T-T-C-G-C-G-3') 2] as a referenced sequence since it has been well studied via 2D NMR. The εC lesion is formed by a reaction with vinyl chloride metabolites or via lipid peroxidation, and base excision repair (BER) is the main pathway to repair this lesion. In order to study this particular sequence, I used 2D solution NMR experiment such as NOESY, TOSCY and HSQC, mapping the 1H chemical shift of the damaged DNA sequence with the intensity of the NOE interactions, compared to the control sequence, to determine the impact of the lesion. My results show the structure changed at the site of lesion and its opposite base pairing partner.
Keywords
Ethenocytidine, DNA, DNA repair, BER, NMR
Subject Categories
Chemistry
Copyright
© Chunling Cao
Recommended Citation
Cao, Chunling, "1H Nmr Examination of DNA Structure Containing 3, N4-Etheno-2'-Deoxycytidine" (2014). MSU Graduate Theses/Dissertations. 2929.
https://bearworks.missouristate.edu/theses/2929
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