Optical photothermal infrared spectroscopy and discrete wavenumber imaging for high content screening of single cells.

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Leibniz Institute of Photonic Technology, Member of Leibniz Research Alliance Leibniz Health Technologies, Member of the Leibniz Center for Photonics in Infection Research, 07745 Jena, Germany.

Published: November 2023

AI Article Synopsis

  • Direct mid-infrared spectroscopic imaging faces challenges like water absorption and low resolution; however, the O-PTIR technique effectively addresses these issues by enabling high-resolution imaging and spectroscopy of single cells in liquid environments.
  • In experiments with leukemia- and cancer-derived cell lines, O-PTIR was able to accurately classify cell types, achieving up to 95.4% accuracy, and revealed detailed subcellular features through specific infrared band analysis.
  • The study highlights O-PTIR's potential for high-quality spectral and imaging analysis of single cells, advancing applications in high-content screening and other biomedical fields.

Article Abstract

Major drawbacks of direct mid-infrared spectroscopic imaging of single cells in an aqueous buffer are strong water absorption, low resolution typically above 10 μm, and Mie scattering effects. This study demonstrates how an indirect detection principle can overcome these drawbacks using the optical photothermal infrared (O-PTIR) technique for high-resolution discrete wavenumber imaging and fingerprint spectroscopy of cultivated cells as a model system in a simple liquid sample chamber. The O-PTIR spectra of six leukemia- and cancer-derived cell lines showed main IR bands near 1648, 1547, 1447, 1400, 1220, and 1088 cm. Five spectra of approximately 260 single cells per cell type were averaged, the O-PTIR data set was divided into leukemia-derived cells (THP-1, HL 60, Jurkat, and Raji) and cancer cells (HeLa and HepaRG), and partial least squares linear discriminant analysis (PLS-LDA) was applied in the spectral range 800-1800 cm to train three classification models. A leukemia cancer cell model showed an accuracy of 90.0%, the HeLa HepaRG cell model had an accuracy of 95.4%, and the model for the distinction of leukemia cells had an accuracy of 75.4%. IR bands in linear discriminants (LDs) of the models were correlated with second derivative spectra that resolved more than 25 subbands. The IR and second derivative spectra of proteins, DNA, RNA and lipids were collected as references to confirm band assignments. O-PTIR images of single cells at a 200 nm step size were acquired at 1086, 1548, and 1746 cm to visualize the nucleic acid, protein, and lipid distribution, respectively. Variations in subcellular features and in the lipid-to-protein and nucleic acid-to-protein ratios were identified that were consistent with biomolecular information in LDs. In conclusion, O-PTIR can provide high-quality spectra and images with submicron resolution of single cells in aqueous buffers that offer prospects in high-content screening applications.

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http://dx.doi.org/10.1039/d3an00902eDOI Listing

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