Compounds for fluorescence sensing of duplex formation
AssigneeSan Diego State University Research Foundation
InventorsByron W. Purse, Dillon Burns, Kristine Teppang, Raymond Lee, Melissa Lokensgard
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AssigneeSan Diego State University Research Foundation
InventorsByron W. Purse, Dillon Burns, Kristine Teppang, Raymond Lee, Melissa Lokensgard
Estimating the term…
Herein reported are new tricyclic cytidine compounds, such as 8-diethylamino-tC (8-DEA-tC), that respond to DNA and/or RNA duplex formation with up to a 20-fold increase in fluorescent quantum yield as compared with the free nucleoside, depending on neighboring bases. This turn-on response to duplex formation is by far the greatest of any reported nucleoside analogue that can participate in Watson-Crick base pairing. Measurements of the quantum yield of 8-DEA-tC mispaired with adenosine and, separately, opposite an abasic site show that there is almost no fluorescence increase without the formation of correct Watson-Crick hydrogen bonds. Kinetic isotope effects from the use of deuterated buffer show that the duplex protects 8-DEA-tC against quenching by excited state proton transfer. DFT calculations provide a rationale for the observed photophysical properties that is dependent on duplex integrity and the electronic structure of the analogue.
A compound of Formula I:
A compound of Formula I:
Dependencies are inferred from the claim text.