Infrared Microscopy of Biochemistry and Metabolism in Single Living Eukaryotic Cells

TL;DR

Infrared microscopy enables real-time biochemical and metabolic analysis of single living eukaryotic cells, offering a versatile and high-throughput approach for metabolomics, toxicology, and pharmacology research.

Contribution

This review highlights recent methodological advances and proof-of-concept experiments in using IR microscopy for live cell biochemical and metabolic studies.

Findings

IR microscopy can detect specific biomolecules in live cells

The technique allows real-time monitoring of metabolic turnover

Current limitations include spatial resolution and sensitivity

Abstract

The turn of the millennium has seen a growing interest in the study of live cells by infrared (IR) spectroscopy, driven by the versatility, wealth of molecular information, and potential for high-throughput screening of the technique. Measurements on individual cells, either isolated or within a multi-cellular structure, provide information that is not available from ensemble samples. The present review discusses the use of infrared (IR) microscopy to analyse live single cells from a biochemical perspective, seeking information on real-time processes. The emphasis is on the use of the technique to quantify metabolic turnover, with the aim of providing a complementary method for metabolomics, and for toxicological and pharmacological studies. The work highlights the methodological advances and proof-of-concept experiments that took place over the past few years in this direction. It discusses current advantages and limitations of the technique, including the possibility of detecting specific biomolecules and their reactivity, and it concludes with a brief outline of future perspectives.