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Updated: Aug 13, 2025

Quantitative Proteomics Workflow using Multiple Reaction Monitoring Based Detection of Proteins from Human Brain Tissue
Published on: August 28, 2021
An LC-MS/MS method for simultaneous analysis of up to six monoamines from brain tissues
Sejal Davla1, Edward Daly2, Jenn Nedow2
1Centre for Research in Neuroscience, Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada; Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada; Integrated Program in Neuroscience, McGill University, Montreal, Quebec, Canada; Brain Repair and Integrative Neuroscience (BRaIN) Program, Research Institute of the McGill University Health Centre, Montreal, Quebec, Canada.
Researchers developed a new LC-MS/MS method to simultaneously quantify six key monoamines, including dopamine and serotonin, in insect and mouse brain tissues. This technique offers precise measurement of crucial neurochemicals for brain function studies.
Area of Science:
- Neuroscience
- Analytical Chemistry
- Biochemistry
Background:
- Monoamines like dopamine and serotonin are vital neuromodulators regulating mood, movement, sleep, and cognition across species.
- The nervous system, from mammals to insects, contains diverse monoamines with varying polarity, posing analytical challenges.
- Accurate quantification of these neurochemicals is essential for understanding brain function and dysfunction.
Purpose of the Study:
- To develop and validate a single-run liquid chromatography-tandem mass spectrometry (LC-MS/MS) method.
- To quantify six distinct monoamines: dopamine (DA), serotonin (5-HT), octopamine (OA), tyramine (TA), melatonin (MT), and N-acetylserotonin (NAS).
- To enable simultaneous analysis of these neurochemicals in precious biological specimens like Drosophila and mouse brain extracts.
Main Methods:
- Liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS).
- Extraction of monoamines from dissected Drosophila and mouse brain tissues.
- Quantitative analysis covering an analytical range of 0.25 to 5.0 ng/mL.
Main Results:
- Successful simultaneous quantification of six key monoamines in a single LC-MS/MS run.
- Demonstrated method's applicability to both insect (Drosophila) and mammalian (mouse) brain tissues.
- Established an analytical range suitable for detecting neurochemical levels in biological samples.
Conclusions:
- The developed LC-MS/MS method provides a robust and efficient tool for simultaneous monoamine quantification.
- This methodology is valuable for neuroscientific research involving comparative studies across species.
- Enables precise measurement of critical neuroactive compounds from limited biological samples.
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