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Full-Text Articles in Physical Sciences and Mathematics
A Procedure For Computing Hydrocarbon Strain Energies Using Computational Group Equivalents, With Application To 66 Molecules, Paul R. Rablen
A Procedure For Computing Hydrocarbon Strain Energies Using Computational Group Equivalents, With Application To 66 Molecules, Paul R. Rablen
Chemistry & Biochemistry Faculty Works
A method is presented for the direct computation of hydrocarbon strain energies using computational group equivalents. Parameters are provided at several high levels of electronic structure theory: W1BD, G-4, CBS-APNO, CBS-QB3, and M062X/6-31+G(2df,p). As an illustration of the procedure, strain energies are computed for 66 hydrocarbons, most of them highly strained.
Biophysical And X-Ray Structural Studies Of The (Gggtt)3ggg G-Quadruplex In Complex With N-Methyl Mesoporphyrin Ix, Linda Yingqi Lin , '20, S. Mccarthy, Barrett M. Powell , '18, Yanti Manurung , '20, Irene M. Xiang , '18, W. L. Dean, B. Chaires, Liliya A. Yatsunyk
Biophysical And X-Ray Structural Studies Of The (Gggtt)3ggg G-Quadruplex In Complex With N-Methyl Mesoporphyrin Ix, Linda Yingqi Lin , '20, S. Mccarthy, Barrett M. Powell , '18, Yanti Manurung , '20, Irene M. Xiang , '18, W. L. Dean, B. Chaires, Liliya A. Yatsunyk
Chemistry & Biochemistry Faculty Works
The G-quadruplex (GQ) is a well-studied non-canonical DNA structure formed by G-rich sequences found at telomeres and gene promoters. Biological studies suggest that GQs may play roles in regulating gene expression, DNA replication, and DNA repair. Small molecule ligands were shown to alter GQ structure and stability and thereby serve as novel therapies, particularly against cancer. In this work, we investigate the interaction of a G-rich sequence, 5’-GGGTTGGGTTGGGTTGGG-3’ (T1), with a water-soluble porphyrin, N-methyl mesoporphyrin IX (NMM) via biophysical and X-ray crystallographic studies. UV-vis and fluorescence titrations, as well as a Job plot, revealed a 1:1 binding stoichiometry with an …