Microchip platforms for multiplex single-cell functional proteomics with applications to immunology and cancer research
Abstract
Single-cell functional proteomics assays can connect genomic information to biological function through quantitative and multiplex protein measurements. Tools for single-cell proteomics have developed rapidly over the past 5 years and are providing approaches for directly elucidating phosphoprotein signaling networks in cancer cells or for capturing high-resolution snapshots of immune system function in patients with various disease conditions. We discuss advances in single-cell proteomics platforms, with an emphasis on microchip methods. These methods can provide a direct correlation of morphological, functional and molecular signatures at the single-cell level. We also provide examples of how those platforms are being applied to both fundamental biology and clinical studies, focusing on immune-system monitoring and phosphoprotein signaling networks in cancer.
Additional Information
© 2013 BioMed Central Ltd. Published: 29 August 2013. Some of the work reviewed here was supported by the National Cancer Institute (5U54 CA119347 and R01 CA170689-01 to JRH) and the National Institutes of Health (NIH 1 U01 CA164252-01 to RF and U54 CA143798 to RF).Attached Files
Published - Wei_2013.pdf
Files
Name | Size | Download all |
---|---|---|
md5:fca2576b3ec8f5483ae68cae22c790ea
|
2.5 MB | Preview Download |
Additional details
- PMCID
- PMC3978720
- Eprint ID
- 41134
- Resolver ID
- CaltechAUTHORS:20130906-082857317
- NIH
- 5U54 CA119347
- NIH
- R01 CA170689-01
- NIH
- 1 U01 CA164252-01
- NIH
- U54 CA143798
- National Cancer Institute
- Created
-
2013-09-16Created from EPrint's datestamp field
- Updated
-
2021-11-10Created from EPrint's last_modified field