Chemiluminescent sensors for quantitation of the bacterial second messenger cyclic di-GMP.

Methods Enzymol

Department of Chemistry and Henry Eyring Center for Cell and Genome Science, University of Utah, Salt Lake City, UT, United States; Department of Chemistry, University of California, Berkeley, Berkeley, CA, United States. Electronic address:

Published: June 2021

Chemiluminescent biosensors have been developed and broadly applied to mammalian cell systems for studying intracellular signaling networks. For bacteria, biosensors have largely relied on fluorescence-based systems for quantitating signaling molecules, but these designs can encounter issues in complex environments due to their reliance on external illumination. In order to circumvent these issues, we designed the first ratiometric chemiluminescent biosensors for studying a key bacterial second messenger, cyclic di-GMP. We have shown recently that these biosensors function both in vitro and in vivo for detecting changes in cyclic di-GMP levels. In this chapter, we present a practical and broadly applicable method for high-throughput quantitation of cyclic di-GMP in bacterial cell extracts using the high affinity biosensor tVYN-TmΔ that could serve as the "Bradford assay" equivalent for this bacterial signaling molecule.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8238376PMC
http://dx.doi.org/10.1016/bs.mie.2020.04.004DOI Listing

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