TY - JOUR
T1 - A fluorescent reporter on electrostatic DNA-ligand interactions
AU - Murade, Chandrashekhar U.
AU - Shubeita, George T.
N1 - Funding Information:
Acknowledgements. This work was supported in part by the National Science Foundation grants PHY-1505020 and PHY-1915119 to GTS. The research was partially carried out using the Core Technology Platform at New York University Abu Dhabi.
Publisher Copyright:
© 2021 Optical Society of America under the terms of the OSA Open Access Publishing Agreement.
PY - 2021
Y1 - 2021
N2 - Among the various types of interactions between biomolecules, electrostatic interactions dominate as these are long-range interactions and are often a generic first step in the recruitment of specific ligands. DNA, being a highly charged molecule, attracts a plethora of molecules. Interactions between DNA and proteins or small molecules shape the overall function of the cell. Various processes such as DNA replication, DNA repair, synthesis of mRNA, and packaging of DNA are mediated by interactions between protein molecules and DNA that are predominantly electrostatic. Here, we present a fluorescence resonance energy transfer (FRET)-based probe which can report on the electrostatic interactions between the negatively-charged DNA and positively-charged metal ions, oligopeptides, as well as DNA groove-binding drug molecules. The simplicity, sensitivity, and versatility of the DNA-based probe makes it suited for applications where specific protein-DNA interactions can be probed, and DNA-binding drugs can be discovered in high-throughput screens of compound libraries. This is particularly relevant given that some of the most potent antitumor and antimicrobial drugs associate with DNA electrostatically.
AB - Among the various types of interactions between biomolecules, electrostatic interactions dominate as these are long-range interactions and are often a generic first step in the recruitment of specific ligands. DNA, being a highly charged molecule, attracts a plethora of molecules. Interactions between DNA and proteins or small molecules shape the overall function of the cell. Various processes such as DNA replication, DNA repair, synthesis of mRNA, and packaging of DNA are mediated by interactions between protein molecules and DNA that are predominantly electrostatic. Here, we present a fluorescence resonance energy transfer (FRET)-based probe which can report on the electrostatic interactions between the negatively-charged DNA and positively-charged metal ions, oligopeptides, as well as DNA groove-binding drug molecules. The simplicity, sensitivity, and versatility of the DNA-based probe makes it suited for applications where specific protein-DNA interactions can be probed, and DNA-binding drugs can be discovered in high-throughput screens of compound libraries. This is particularly relevant given that some of the most potent antitumor and antimicrobial drugs associate with DNA electrostatically.
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U2 - 10.1364/BOE.439791
DO - 10.1364/BOE.439791
M3 - Article
AN - SCOPUS:85122023370
SN - 2156-7085
VL - 13
SP - 159
EP - 167
JO - Biomedical Optics Express
JF - Biomedical Optics Express
IS - 1
ER -