Automated Optically Guided System for Chemical Analysis of Single Plant and Algae Cells Using Laser Microdissection/Liquid Vortex Capture/Mass Spectrometry

• Published in: Frontiers in plant science Vol. 9; p. 1211
• Main Authors: Cahill, John F, Kertesz, Vilmos
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Research Foundation 20.08.2018; Frontiers Media S.A
• Subjects: algae; BASIC BIOLOGICAL SCIENCES; classification; laser microdissection; liquid capture; mass spectrometry; Plant Science; single cell; single cell; algae; laser microdissection; mass spectrometry; automated analysis; classification; liquid capture; high throughput
• ISSN: 1664-462X; 1664-462X
• DOI: 10.3389/fpls.2018.01211

Current analytical methods are not capable of providing rapid, sensitive, and comprehensive chemical analysis of a wide range of cellular constitutes of single cells (e.g., lipids, metabolites, proteins, etc.) from dispersed cell suspensions and thin tissues. This capability is important for a number of critical applications, including discovery of cellular mechanisms for coping with chemical or environmental stress and cellular response to drug treatment, to name a few. Here we introduce an optically guided platform and methodology for rapid, automated recognition, sampling, and chemical analysis of surface confined individual cells utilizing a novel hybrid laser capture microdissection/liquid vortex capture/mass spectrometry system. The system enabled automated analysis of single cells by reliably detecting and sampling them either through laser ablation from a glass microscope slide or by cutting the entire cell out of a poly(ethylene naphthalate)-coated membrane substrate that the cellular sample is deposited on. Proof of principle experiments were performed using thin tissues of and cultured and cell suspensions as model systems for single cell analysis using the developed method. Reliable, hands-off laser ablation sampling coupled to liquid vortex capture/mass spectrometry analysis was conducted for hundreds of individual cells in connected tissue. In addition, more than 300 individual and cells were analyzed automatically and sampled using laser microdissection sampling with the same liquid vortex capture/mass spectrometry analysis system. Principal component analysis-linear discriminant analysis, applied to each mass spectral dataset, was used to determine the accuracy of differentiation of the different algae cell lines.