Influence of the geometry of fluorescently labelled DNA constructs on fluorescence anisotropy assay

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Publikace nespadá pod Fakultu sportovních studií, ale pod Přírodovědeckou fakultu. Oficiální stránka publikace je na webu muni.cz.
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BROM Tomáš REDDAVIDE Francesco V HEIDEN Stephan THOMPSON Michael ZHANG Yixin

Rok publikování 2020
Druh Článek v odborném periodiku
Časopis / Zdroj Biochemical and biophysical research communications
Fakulta / Pracoviště MU

Přírodovědecká fakulta

Citace
www https://www.sciencedirect.com/science/article/pii/S0006291X2030749X
Doi http://dx.doi.org/10.1016/j.bbrc.2020.04.025
Klíčová slova Fluorescence anisotropy; DNA-Encoded chemical library; Drug discovery; Hit validation; Small molecules
Přiložené soubory
Popis DNA-encoded chemical libraries (DECLs) are powerful tools for modern drug discovery. A DECL is apooled mixture of small molecule compounds, each of which is tagged with a unique DNA sequencewhich functions as a barcode. After incubation with a drug target and washing to remove non-binders,the bound molecules are eluted and submitted for DNA sequencing to determine which molecules arebinding the target. While the DECL technology itself is ultra-high throughput, the following re-synthesisof identified compounds for orthogonal validation experiments remains the bottleneck. Using existingDNA-small molecule conjugates directly for affinity measurements, as opposed to complete compoundresynthesis, could accelerate the discovery process. To this end, we have tested various geometries offluorescently-labelled DNA constructs forfluorescence anisotropy (FA) experiments. Minimizing thedistance between thefluorescent moiety and ligand can maximize the correlation between ligand-protein interaction and corresponding change influorophore rotational freedom, thus leading tolarger, easier to interpret changes in FA values. However, close proximity can also cause artifacts due topotentially promiscuous interactions betweenfluorophore and protein. By balancing these two oppositeeffects, we have identified applicablefluorescently labelled DNA constructs displaying either a singleligand or pairs of fragments for affinity measurement using a FA assay.
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