Correlative Fluorescence and Raman Microscopy to Define Mitotic Stages at the Single-Cell Level: Opportunities and Limitations in the AI Era.

Journal: Biosensors
Published Date:

Abstract

Nowadays, morphology and molecular analyses at the single-cell level have a fundamental role in understanding biology better. These methods are utilized for cell phenotyping and in-depth studies of cellular processes, such as mitosis. Fluorescence microscopy and optical spectroscopy techniques, including Raman micro-spectroscopy, allow researchers to examine biological samples at the single-cell level in a non-destructive manner. Fluorescence microscopy can give detailed morphological information about the localization of stained molecules, while Raman microscopy can produce label-free images at the subcellular level; thus, it can reveal the spatial distribution of molecular fingerprints, even in live samples. Accordingly, the combination of correlative fluorescence and Raman microscopy (CFRM) offers a unique approach for studying cellular stages at the single-cell level. However, subcellular spectral maps are complex and challenging to interpret. Artificial intelligence (AI) may serve as a valuable solution to characterize the molecular backgrounds of phenotypes and biological processes by finding the characteristic patterns in spectral maps. The major contributions of the manuscript are: () it gives a comprehensive review of the literature focusing on AI techniques in Raman-based cellular phenotyping; () via the presentation of a case study, a new neural network-based approach is described, and the opportunities and limitations of AI, specifically deep learning, are discussed regarding the analysis of Raman spectroscopy data to classify mitotic cellular stages based on their spectral maps.

Authors

  • Csaba Voros
    Synthetic and Systems Biology Unit, Biological Research Centre (BRC), Temesvári krt. 62, H-6726 Szeged, Hungary.
  • Dávid Bauer
    Department of Cardiology, University Hospital Královské Vinohrady, Prague, Czech Republic.
  • Ede Migh
    Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Istvan Grexa
    Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Attila Gergely Végh
    Institute of Biophysics, Biological Research Centre (BRC), Temesvári krt. 62, H-6726 Szeged, Hungary.
  • Balázs Szalontai
    Institute of Biophysics, Biological Research Centre (BRC), Temesvári krt. 62, H-6726 Szeged, Hungary.
  • Gastone Castellani
    Department of Specialised, Diagnostic and Experimental Medicine, University of Bologna, 40126, Bologna, BO, Italy.
  • Tivadar Danka
    Institute of Biochemistry, Biological Research Centre of the Hungarian Academy of Sciences, H-6726 Szeged, Hungary.
  • Sašo Džeroski
    Dept. of Knowledge Technologies, Jožef Stefan Institute, Jamova 39, 1000 Ljubljana, Slovenia.
  • Krisztian Koos
    Synthetic and Systems Biology Unit, Hungarian Academy of Sciences, Biological Research Center (BRC), Temesvári körút 62, Szeged 6726, Hungary.
  • Filippo Piccinini
    Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Meldola, FC, Italy.
  • Péter Horváth
    Department of Pulmonology, Semmelweis University, Budapest, Hungary.