AI Article Synopsis

  • pH-sensitive fluorescent proteins provide a novel way to monitor pH levels in and outside cells, but there are few options for ratiometric sensors that can be easily purified.
  • Researchers successfully fused the protein CoGFP_V0 with epidermal growth factor (EGF), creating two effective pH sensors (EGF-CoGFP-mTagBFP2 and EGF-CoGFP-mCRISPRed) that exhibit a wide pH detection range and maintain their fluorescence properties.
  • These sensors enable detailed intracellular pH mapping through live-cell microscopy, track pH changes in microfluidic environments, and enhance ratiometric flow cytometry, offering insights into internalization rates for evaluating protein-drug conjugates in cancer treatment.

Article Abstract

pH-sensitive fluorescent proteins as genetically encoded pH sensors are promising tools for monitoring intra- and extracellular pH. However, there is a lack of ratiometric pH sensors, which offer a good dynamic range and can be purified and applied extracellularly to investigate uptake. In our study, the bright fluorescent protein CoGFP_V0 was C-terminally fused to the ligand epidermal growth factor (EGF) and retained its dual-excitation and dual-emission properties as a purified protein. The tandem fluorescent variants EGF-CoGFP-mTagBFP2 (pK' = 6.6) and EGF-CoGFP-mCRISPRed (pK' = 6.1) revealed high dynamic ranges between pH 4.0 and 7.5. Using live-cell fluorescence microscopy, both pH sensor molecules permitted the conversion of fluorescence intensity ratios to detailed intracellular pH maps, which revealed pH gradients within endocytic vesicles. Additionally, extracellular binding of the pH sensors to cells expressing the EGF receptor (EGFR) enabled the tracking of pH shifts inside cultivation chambers of a microfluidic device. Furthermore, the dual-emission properties of EGF-CoGFP-mCRISPRed upon 488 nm excitation make this pH sensor a valuable tool for ratiometric flow cytometry. This high-throughput method allowed for the determination of internalization rates, which represents a promising kinetic parameter for the in vitro characterization of protein-drug conjugates in cancer therapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9138566PMC
http://dx.doi.org/10.3390/bios12050271DOI Listing

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