Identification of Tunable, Environmentally Responsive Fluorogenic Dyes by High-Throughput Screening

Small molecule dyes remain essential biological tools, yet only a handful of environmentally responsive fluorogenic small molecules are available for routine characterization of protein state. Here, we report the development and execution of a high throughput screen to identify compounds that increase in fluorescence in response to binding of lipophilic sites of proteins. This effort yielded two small molecules that potently indicate the presence of a range of common proteins and outperform common dyes in differential scanning fluorimetry experiments. Structure activity relationship studies revealed that these two scaffolds can be tuned both for their quantum yields and emission wavelengths. This work affords a straightforward framework for the discovery of new fluorophores and adds two fluorogenic probes to the toolbox for studying protein state.

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Publication Details

Journal
ACS Chemical Biology
Published
2024-09-09
DOI
https://doi.org/10.1021/acschembio.4c00373
Citations
3
Primary Topic
Advanced Biosensing Techniques and Applications
Type
article
Field-Weighted Citation Impact
0.70

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article

Identification of Tunable, Environmentally Responsive Fluorogenic Dyes by High-Throughput Screening

Michael J. Bollong, Shaochen You, Chloris Li-Ma, Thu Nguyen
3 citations
ACS Chemical Biology
Advanced Biosensing Techniques and Applications
0.70
article

Identification of Tunable, Environmentally Responsive Fluorogenic Dyes by High-Throughput Screening

Michael J. Bollong, Shaochen You, Chloris Li-Ma, Thu Nguyen
article en
3 citations

Abstract

Small molecule dyes remain essential biological tools, yet only a handful of environmentally responsive fluorogenic small molecules are available for routine characterization of protein state. Here, we report the development and execution of a high throughput screen to identify compounds that increase in fluorescence in response to binding of lipophilic sites of proteins. This effort yielded two small molecules that potently indicate the presence of a range of common proteins and outperform common dyes in differential scanning fluorimetry experiments. Structure activity relationship studies revealed that these two scaffolds can be tuned both for their quantum yields and emission wavelengths. This work affords a straightforward framework for the discovery of new fluorophores and adds two fluorogenic probes to the toolbox for studying protein state.

ACS Chemical BiologyVol. 19(9)
Scripps Institution of Oceanography (US), Scripps (United States) (US)
National Institutes of Health, National Institute of General Medical Sciences
Zero hunger
Openalex Percentile: Top 30%
Advanced Biosensing Techniques and Applications
0.70
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