FP6Individual fellowship2007–2010

NEUROANALYTCHEM · Ultra-small analytical techniques applied to single cell neurochemistry

FP6 — Marie Curie Actions (Human Resources and Mobility)

Duration
2007-05-01 → 2010-04-30
EU contribution
€691,470
Participants
1
Scheme
EIF

Lines connect the coordinator with its partners. CORDIS does not always give exact coordinates for projects before 2014. These points are placed at city or country level.

Results in brief

Final Activity Report Summary - NEUROANALYTCHEM (Ultrasmall analytical techniques applied to single cell neurochemistry)

The Marie Curie Chair was used to train new scientists and to develop several new analytical chemistry methods. Major progress was made in developing new methods of mass spectrometry imaging of lipids on single cells and to use this to understand the way by which cells use different lipids to control their function. Significant progress was also made in developing new electrochemical tools to measure neurotransmitters coming from single cells during cell-to-cell communication. In a third area, new approaches to measure the levels of transmitters and metabolites in the dissected brains of fruit flies and also to directly measure the transmitter levels in the brain during function of the live fly have been developed and published. Our most recent new technology has been to develop a method we call electrochemical cytometry allowing us to measure the amounts of transmitters in single vesicles in a high-throughput manner so we can determine the levels in thousands of vesicles in one run taking only a few hours. This method is sensitive to 1800 molecules in a single vesicle. This work opens the door for quantitative measurements of individual neuronal cells while they communicate with other cells in a network, and the vesicles they use to communicate with, in models of diseases like Parkinson's and Alzheimer's disease. It is analytical techniques like these that will be a part of future breakthroughs in these areas. During this three-year period published 30 peer-reviewed papers in highly respectable journals including Proceedings of the National Academy of Science, Analytical Chemistry and ACS Chemical Neuroscience as well as 4 invited papers/book chapters and the researcher gave 32 invited presentations on this work around the world.

Data: CORDIS, © European Union

Project objective

It is proposed to develop and apply ultra-small volume analytical chemistry techniques to measure molecules important in single cell neurochemistry and neurobiology. The importance of this work to the scientific community lies in that it defines the limits for measurements in small biological environments and it provides a means to examine molecular mechanisms of neuronal function and dysfunction (ilness). Techniques using microelectrode electrochemistry will be used to measure release of transmitters from single cells. Separations with micrometer and nanometer inner diameter capillary electrophoresis will be used to measure neurochemicals in spatially localized regions of cells and organelles. Mass spectrometry imaging with submicrometer resolution will be developed to measure and determine the function of lipid domains in cell membranes. It is my goal to unify these techniques and measurements to provide a comprehensive view of the location, function and importance of membrane lipids regulating communicatio n via exocytosis. In addition, we will relate this function to the role of exocytosis proteins in regulating the exocytosis event. This project will involve new developments in each technique area and applied analytical chemistry for bioanalytical measurem ents in neurochemistry.

Original text from CORDIS.

Participants

  • GÖTEBORG UNIVERSITY · GÖTEBORGCoordinatorCity levelSweden

Links

Data: CORDIS, © European Union