Nature Communications (Oct 2018)
Chemical and structural studies provide a mechanistic basis for recognition of the MYC G-quadruplex
- David R. Calabrese,
- Xiang Chen,
- Elena C. Leon,
- Snehal M. Gaikwad,
- Zaw Phyo,
- William M. Hewitt,
- Stephanie Alden,
- Thomas A. Hilimire,
- Fahu He,
- Aleksandra M. Michalowski,
- John K. Simmons,
- Lindsey B. Saunders,
- Shuling Zhang,
- Daniel Connors,
- Kylie J. Walters,
- Beverly A. Mock,
- John S. Schneekloth
Affiliations
- David R. Calabrese
- Chemical Biology Laboratory, National Cancer Institute
- Xiang Chen
- Structural Biophysics Laboratory, National Cancer Institute
- Elena C. Leon
- Laboratory of Cancer Biology and Genetics, National Cancer Institute
- Snehal M. Gaikwad
- Laboratory of Cancer Biology and Genetics, National Cancer Institute
- Zaw Phyo
- Laboratory of Cancer Biology and Genetics, National Cancer Institute
- William M. Hewitt
- Chemical Biology Laboratory, National Cancer Institute
- Stephanie Alden
- Chemical Biology Laboratory, National Cancer Institute
- Thomas A. Hilimire
- Chemical Biology Laboratory, National Cancer Institute
- Fahu He
- Structural Biophysics Laboratory, National Cancer Institute
- Aleksandra M. Michalowski
- Laboratory of Cancer Biology and Genetics, National Cancer Institute
- John K. Simmons
- Laboratory of Cancer Biology and Genetics, National Cancer Institute
- Lindsey B. Saunders
- Chemical Biology Laboratory, National Cancer Institute
- Shuling Zhang
- Laboratory of Cancer Biology and Genetics, National Cancer Institute
- Daniel Connors
- Laboratory of Cancer Biology and Genetics, National Cancer Institute
- Kylie J. Walters
- Structural Biophysics Laboratory, National Cancer Institute
- Beverly A. Mock
- Laboratory of Cancer Biology and Genetics, National Cancer Institute
- John S. Schneekloth
- Chemical Biology Laboratory, National Cancer Institute
- DOI
- https://doi.org/10.1038/s41467-018-06315-w
- Journal volume & issue
-
Vol. 9,
no. 1
pp. 1 – 15
Abstract
Targeting noncoding nucleic acids with small molecules represents an important and significant challenge in chemical biology and drug discovery. Here the authors characterize DC-34, a small molecule that exhibits selective binding to specific G4 structures, and provide a structural basis for its selectivity