A single-phase flow microfluidic cell sorter for multiparameter screening to assist the directed evolution of Ca<sup>2+</sup> sensors.
basic_science · Level V
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- Record sourced from PubMed, PMID 31641712.
- Also identified by DOI 10.1039/c9lc00779b.
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Abstract
We introduce a single-phase flow microfluidic cell sorter with a two-point detection system capable of two-parameter screening to assist with directed evolution of a fluorescent protein based Ca<sup>2+</sup> sensor expressed in bacterial cells. The new cell sorting system utilizes two fluorescence microscopes to obtain signals at two different points along a flow path in which a change in concentration of the analyte, Ca<sup>2+</sup>, is induced. The two detectors thus determine the magnitude of fluorescence change of the sensor following the reaction, along with the overall brightness of the sensor. A design for a 3D focusing flow was configured to enhance the spatial control of cells and signal pair-matching. The cell sorter screens the sensors at a moderate throughput, 10 cells per s and 10<sup>5</sup> cells per round, enriching top variants for the subsequent manual screening with higher accuracy. Our new μFACS greatly accelerates the directed evolution of genetically encoded Ca<sup>2+</sup> sensors compared to the previous version with single point detection for brightness-based screening. Two rounds of directed evolution led to a variant, named Y-GECO2f, which exhibits a 26% increase in brightness and a greater than 300% larger Ca<sup>2+</sup>-dependent fluorescence change in vitro relative to the variant before evolution.
Medical subject headings
- Calcium
- Flow Cytometry
- Microfluidic Analytical Techniques