@article{Kuru_E-2024_212962,
title = {Rapid discovery and evolution of nanosensors containing fluorogenic amino acids},
author = {Kuru, E. and Rittichier, J. and Flores, A. and Rout, S. and Han, I. and Reese, A. and Bartlett, T. and Bernier, S. and Galpin, J. and Marchand, J. and Bedell, W. and Robinson-McCarthy, L. and Ahern, C. and Bernhardt, T. and Rudner, D. and Collins, J. and Vendrell, M. and Church, G. and de Puig, H. and de Moliner, F.},
month = {sep},
year = {2024},
abstract = {Binding-activated optical sensors are powerful tools for imaging, diagnostics, and biomolecular sensing. However, biosensor discovery is slow and requires tedious steps in rational design, screening, and characterization. Here we report on a platform that streamlines biosensor discovery and unlocks directed nanosensor evolution through genetically encodable fluorogenic amino acids (FgAAs). Building on the classical knowledge-based semisynthetic approach, we engineer ~15 kDa nanosensors that recognize specific proteins, peptides, and small molecules with up to 100-fold fluorescence increases and subsecond kinetics, allowing real-time and wash-free target sensing and live-cell bioimaging. An optimized genetic code expansion chemistry with FgAAs further enables rapid (~3 h) ribosomal nanosensor discovery via the cell-free translation of hundreds of candidates in parallel and directed nanosensor evolution with improved variant-specific sensitivities (up to ~250-fold) for SARS-CoV-2 antigens. Altogether, this platform could accelerate the discovery of fluorogenic nanosensors and pave the way to modify proteins with other non-standard functionalities for diverse applications.},
volume = {15},
journal = {Nature Communications},
publisher = {Springer Nature},
url = {https://doi.org/10.1038/s41467-024-50956-z},
}
