Continuous cell sorting in a flow based on single cell resonance Raman spectra. Issue 8 (14th March 2016)

• Record Type: Journal Article
• Authors: McIlvenna, David; Huang, Wei E.; Davison, Paul; Glidle, Andrew; Cooper, Jon; Yin, Huabing
• Is Part Of: Lab on a chip. Volume 16:Issue 8(2016)
• Page Start: 1420
• Page End: 1429
• Publication Date: 2016-03-14
• Subjects: Miniature electronic equipment -- Periodicals; Combinatorial chemistry -- Periodicals; Biotechnology -- Periodicals; 543.0813
• DOI: 10.1039/c6lc00251j
• Languages: English
• ISSNs: 1473-0197

Abstract

Abstract : A chip-based Raman activated cell sorting system is developed, which demonstrates continuous and automated sorting of individual cells in a flow, based on their intrinsic resonance Raman spectra. This platform allows the isolation of cells in their native fluid with the ability to achieve high accuracy sorting of 96.3%. Abstract : Single cell Raman spectroscopy measures a spectral fingerprint of the biochemistry of cells, and provides a powerful method for label-free detection of living cells without the involvement of a chemical labelling strategy. However, as the intrinsic Raman signals of cells are inherently weak, there is a significant challenge in discriminating and isolating cells in a flowing stream. Here we report an integrated Raman-microfluidic system for continuous sorting of a stream of cyanobacteria, Synechocystis sp. PCC6803. These carotenoid-containing microorganisms provide an elegant model system enabling us to determine the sorting accuracy using the subtly different resonance Raman spectra of microorganism cultured in a 12 C or 13 C carbon source. Central to the implementation of continuous flow sorting is the use of "pressure dividers" that eliminate fluctuations in flow in the detection region. This has enabled us to stabilise the flow profile sufficiently to allow automated operation with synchronisation of Raman acquisition, real-time classification and sorting at flow rates of ca. <100 μm s −1, without the need to "trap" the cells. We demonstrate the flexibility of this approach in sorting mixed cell populations with the ability to achieve 96.3% purity of the selected cells at a speed of 0.5 Hz.