Novel DNA-binding ligands with sequence selectivity based on hydrophobic structure.

3Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

We have developed diamino-bistetrahydrofuran compounds (diamino-bisTHF) as new DNA binding molecules. Diamino-bisTHF (3:RR8) stabilized GC-rich duplex DNA with sequence specificity. DNA binding affinity increased as the alkyl chain was lengthened, indicating that the hydrophobic interaction is essential for DNA binding. It was also found that DNA binding affinity of the ligands depends on the stereochemistry of the amino group. In thermodynamic evaluation, diamino-bisTHF (3:RR8) showed a high affinity to the 12 bp duplex at a molar ratio of 1:1.

Cite

CITATION STYLE

APA

Shibata, T., Torigoe, H., Shibata, Y., Maeda, M., & Sasaki, S. (1999). Novel DNA-binding ligands with sequence selectivity based on hydrophobic structure. Nucleic Acids Symposium Series, (42), 251–252. https://doi.org/10.1093/nass/42.1.251

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free