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Hybridization-Sensitive Fluorescent Probes for DNA and RNA by a Modular “Click” Approach

Gebhard, Julian ORCID iD icon 1; Hirsch, Lara 1; Schwechheimer, Christian 1; Wagenknecht, Hans-Achim 1
1 Institut für Organische Chemie (IOC), Karlsruher Institut für Technologie (KIT)

Abstract:

Fluorescent DNA probes were prepared in a modular approach using the “click” post-synthetic modification strategy. The new glycol-based module and DNA building block place just two carbons between the phosphodiester bridges and anchor the dye by an additional alkyne group. This creates a stereocenter in the middle of this artificial nucleoside substitute. Both enantiomers and a variety of photostable cyanine–styryl dyes as well as thiazole orange derivatives were screened as “clicked” conjugates in different surrounding DNA sequences. The combination of the (S)-configured DNA anchor and the cyanylated cyanine–styryl dye shows the highest fluorescence light-up effect of 9.2 and a brightness of approximately 11,000 M–1 cm–1. This hybridization sensitivity and fluorescence readout were further developed utilizing electron transfer and energy transfer processes. The combination of the hybridization-sensitive DNA building block with the nucleotide of 5-nitroindole as an electron acceptor and a quencher increases the light-up effect to 20 with the DNA target and to 15 with the RNA target. The fluorescence readout could significantly be enhanced to values between 50 and 360 by the use of energy transfer to a second DNA probe with commercially available dyes, like Cy3.5, Cy5, and Atto590, as energy acceptors at the 5′-end. ... mehr


Verlagsausgabe §
DOI: 10.5445/IR/1000150130
Veröffentlicht am 23.08.2022
Originalveröffentlichung
DOI: 10.1021/acs.bioconjchem.2c00241
Scopus
Zitationen: 8
Dimensions
Zitationen: 8
Cover der Publikation
Zugehörige Institution(en) am KIT Institut für Organische Chemie (IOC)
Publikationstyp Zeitschriftenaufsatz
Publikationsjahr 2022
Sprache Englisch
Identifikator ISSN: 1043-1802, 1520-4812
KITopen-ID: 1000150130
Erschienen in Bioconjugate Chemistry
Verlag American Chemical Society (ACS)
Band 33
Heft 9
Seiten 1634–1642
Vorab online veröffentlicht am 22.08.2022
Nachgewiesen in Dimensions
Web of Science
Scopus
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