Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.676913
Title: Novel method for high throughput FRET screening with microfluidics
Author: Visitkul, Viput
Awarding Body: King's College London
Current Institution: King's College London (University of London)
Date of Award: 2013
Availability of Full Text:
Access through EThOS:
Access through Institution:
Abstract:
Functional imaging can provide a level of quantification that is not possible in what might be termed traditional high-content screening. This is due to the fact that the current state-of-the-art high-content screening systems take the approach of scaling-up single cell assays, and are therefore based on essentially pictorial measures as assay indicators. Such phenotypic analyses have become extremely sophisticated, advancing screening enormously, but this approach can still be somewhat subjective. Recent advances in high-content screening with functional read-outs such as FRET (by FLIM or anisotropy imaging) have enabled screening of compound libraries of inhibitors and siRNA against a known protein interaction readout but this is still relatively slow in comparison to true high throughput methodologies. In order to further increase the predictive and statistical power of functional FRET assays, we have developed a compact lifetime-based flow cytometer, utilising a commercial microfluidic chip, to screen large non-adherent cell population. Fluorescent signals from cells are detected using time correlated single photon counting (TCSPC) in the burst integrated fluorescence lifetime (BIFL) mode and used to determine the fluorescence lifetime of each cell. Initially, the system was tested using 2 μm and 10 μm highly fluorescent beads to determine optical throughput and detection efficiency. The system was validated with a number of cell lines transiently transfected with FRET standards, consisting of eGFP and mRFP1 fluorescent proteins linked by 7, 19, and 32 amino acid chains. Analysis software was developed to process detected signals in BIFL mode and chronologically save the transient burst data for each cell in a multidimensional image file. Furthermore, the system was validated using an EGFR phosphorylation assay in MCF7 cells to ascertain the sensitivity of the system for protein-protein interaction screening with a transfected protein and a labelled antibody.
Supervisor: Ameer-Beg, Simon ; Suhling, Klaus Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.676913  DOI: Not available
Share: