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A Label-free Technique for the Spatio-temporal Imaging of Single Cell Secretions
Published on: November 23, 2015
Electrochemiluminescence to detect surface proteins on live cells
Yanmei Lu1, Judy Young, Y Gloria Meng
1Department of Assay and Automation Technology, Genentech Inc., South San Francisco, CA 94080, United States.
Current Opinion in Pharmacology
|September 18, 2007
Summary
A new electrochemiluminescent assay offers a high-throughput method for detecting surface proteins on live cells. This advanced technique simplifies cell analysis by eliminating centrifugation and cell detachment steps.
Area of Science:
- Biotechnology
- Cell Biology
- Analytical Chemistry
Background:
- Traditional methods like flow cytometry and ELISAs detect cell surface proteins.
- These methods often involve complex washing steps requiring centrifugation or cell detachment.
Purpose of the Study:
- To introduce and evaluate an electrochemiluminescent (ECL) assay as an alternative for surface protein detection.
- To highlight the advantages of ECL assays over conventional methods for both suspension and adherent cells.
Main Methods:
- Utilized a novel electrochemiluminescent assay with carbon surface electrodes in microwell plates.
- Assessed the binding of suspension cells and the culturing/analysis of adherent cells (human umbilical vein endothelial cells) directly in the ECL plates.
Main Results:
- Carbon surface plates effectively bind suspension cells, enabling washing with a plate washer and eliminating centrifugation.
- Adherent cells can be cultured, activated, and assayed in the same plate, removing the need for cell detachment.
- The ECL assay demonstrated a high-throughput capability for detecting surface proteins on live cells.
Conclusions:
- The electrochemiluminescent assay provides a streamlined and efficient alternative to flow cytometry and ELISAs for surface protein detection.
- This technology simplifies workflows for both suspension and adherent cell types, enhancing ease of use and throughput.
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