Synthesis of Substituted Flavone Derivatives for Triplex Binding

Poster Number

19C

Lead Author Major

Biochemistry

Lead Author Status

Sophomore

Format

Poster Presentation

Faculty Mentor Name

Liang Xue

Faculty Mentor Department

Chemistry Department

Graduate Student Mentor Name

Nghia Tran

Graduate Student Mentor Department

Chemistry Department

Additional Mentors

Landy Gu, l_gu2@u.pacific.edu, Chemistry Department

Vanessa Rangel, v_rangel1@u.pacific.edu, Chemistry Department

Abstract/Artist Statement

Triplex DNA is a DNA structure composed of three strands of DNA. Triplexes can form intramolecularly and intermolecularly. Intramolecular triplex formation occurs when a DNA strand folds on itself and forms Hoogsteen H-bonds. Intermolecular triplex formation occurs when a third external strand is introduced and binds to the duplex, and forms Hoogsteen bonds. This third strand is known as a triplex-forming oligonucleotide (TFO). Triplex research has become more relevant because of its potential for antigene therapy. The binding of TFOs to specific regions of the DNA can alter the transcription and translation of certain genes. This can be used to silence certain regions of the DNA responsible for genetic diseases and even cancer. Previously, our group found that 5-substituted quercetin derivatives strongly bind to triplex DNA while having minimal impact on duplex DNA. In this report, I will present the synthesis of quercetin derivatives with an amino-containing side chain at different positions and evaluate their ability to stabilize triplex DNA using thermal denaturation monitored by UV.

Location

Information Commons, William Knox Holt Memorial Library and Learning Center

Start Date

29-4-2023 10:00 AM

End Date

29-4-2023 1:00 PM

This document is currently not available here.

Share

COinS
 
Apr 29th, 10:00 AM Apr 29th, 1:00 PM

Synthesis of Substituted Flavone Derivatives for Triplex Binding

Information Commons, William Knox Holt Memorial Library and Learning Center

Triplex DNA is a DNA structure composed of three strands of DNA. Triplexes can form intramolecularly and intermolecularly. Intramolecular triplex formation occurs when a DNA strand folds on itself and forms Hoogsteen H-bonds. Intermolecular triplex formation occurs when a third external strand is introduced and binds to the duplex, and forms Hoogsteen bonds. This third strand is known as a triplex-forming oligonucleotide (TFO). Triplex research has become more relevant because of its potential for antigene therapy. The binding of TFOs to specific regions of the DNA can alter the transcription and translation of certain genes. This can be used to silence certain regions of the DNA responsible for genetic diseases and even cancer. Previously, our group found that 5-substituted quercetin derivatives strongly bind to triplex DNA while having minimal impact on duplex DNA. In this report, I will present the synthesis of quercetin derivatives with an amino-containing side chain at different positions and evaluate their ability to stabilize triplex DNA using thermal denaturation monitored by UV.