Infrared multiple photon dissociation (IRMPD) spectroscopy and its potential for the clinical laboratory
Vibrational spectroscopy
Mass spectrometry
Metabolites
Medical technology
Pharmaceuticals
R855-855.5
Advances in MS Instrumentation: The Present and Future of the Clinical Lab
Infrared multiple photon dissociation spectroscopy
01 natural sciences
Post-translational modifications
0104 chemical sciences
DOI:
10.1016/j.jmsacl.2021.12.004
Publication Date:
2021-12-14T17:52:06Z
AUTHORS (2)
ABSTRACT
Infrared multiple photon dissociation (IRMPD) spectroscopy is a powerful tool used to probe the vibrational modes-and, by extension, the structure-of an ion within an ion trap mass spectrometer. Compared to traditional FTIR spectroscopy, IRMPD spectroscopy has advantages including its sensitivity and its relative ability to handle complex mixtures. While IRMPD has historically been a technique for fundamental analyses, it is increasingly being applied in a more analytical fashion. Notable recent demonstrations pertinent to the clinical laboratory and adjacent interests include analysis of modified amino acids/residues and carbohydrates, structural elucidation (including isomeric differentiation) of metabolites, identification of novel illicit drugs, and structural studies of various biomolecules and pharmaceuticals. Improvements in analysis time, coupling to commercial instruments, and integration with separations methods are all drivers toward the realization of these analytical applications. Additional improvements in these areas, along with advances in benchtop tunable IR sources and increased cross-discipline collaboration, will continue to drive innovation and widespread adoption. The goal of this tutorial article is to briefly present the fundamentals and instrumentation of IRMPD spectroscopy, as an overview of the utility of this technique for helping to answer questions relevant to clinical analysis, and to highlight limitations to widespread adoption, as well as promising directions in which the field may be heading.
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