Issue 34, 2017

pH-Responsive quencher-free molecular beacon systems containing 2′-deoxyuridine units labeled with fluorene derivatives

Abstract

Three fluorescent nucleosides—UFL, UAF, and UDAF, containing fluorene, 2-aminofluorene, and 2-dimethylaminofluorene units, respectively, covalently attached to 2′-deoxyuridine—have been incorporated into the central positions of oligodeoxynucleotides (ODNs) to examine the effects of their flanking bases (FBs) and pH on the emission properties upon hybridization with fully matched and single-base-mismatched targets. The ODN containing UFL and cytosine-FBs in the pH range from 5.5 to 8.0 and the ODN containing UDAF and cytosine-FBs under slightly acidic conditions (pH 6.0–6.5) exhibited dramatic increases in fluorescence only upon duplex formation with their fully matched target DNAs.

Graphical abstract: pH-Responsive quencher-free molecular beacon systems containing 2′-deoxyuridine units labeled with fluorene derivatives

Supplementary files

Article information

Article type
Paper
Submitted
11 Jul 2017
Accepted
09 Aug 2017
First published
09 Aug 2017

Org. Biomol. Chem., 2017,15, 7165-7172

pH-Responsive quencher-free molecular beacon systems containing 2′-deoxyuridine units labeled with fluorene derivatives

J. W. Lee, Y. Son, J. Y. Hwang, Y. Park and G. T. Hwang, Org. Biomol. Chem., 2017, 15, 7165 DOI: 10.1039/C7OB01703K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements