Journal article
Single-molecule level analysis of the subunit composition of the T cell receptor on live T cells
- Abstract:
- The T cell receptor (TCR) expressed on most T cells is a protein complex consisting of TCRαβ heterodimers that bind antigen and cluster of differentiation (CD) 3εδ, εγ, and ζζ dimers that initiate signaling. A long-standing controversy concerns whether there is one, or more than one, αβ heterodimer per complex. We used a form of single-molecule spectroscopy to investigate this question on live T cell hybridomas. The method relies on detecting coincident fluorescence from single molecules labeled with two different fluorophores, as the molecules diffuse through a confocal volume. The fraction of events that are coincident above the statistical background is defined as the "association quotient," Q. In control experiments, Q was significantly higher for cells incubated with wheat germ agglutinin dual-labeled with Alexa488 and Alexa647 than for cells incubated with singly labeled wheat germ agglutinin. Similarly, cells expressing the homodimer, CD28, gave larger values of Q than cells expressing the monomer, CD86, when incubated with mixtures of Alexa488- and Alexa647-labeled antibody Fab fragments. T cell hybridomas incubated with mixtures of anti-TCRβ Fab fragments labeled with each fluorophore gave a Q value indistinguishable from the Q value for CD86, indicating that the dominant form of the TCR comprises single αβ heterodimers. The values of Q obtained for CD86 and the TCR were low but nonzero, suggesting that there is transient or nonrandom confinement, or diffuse clustering of molecules at the T cell surface. This general method for analyzing the subunit composition of protein complexes could be extended to other cell surface or intracellular complexes, and other living cells. © 2007 by The National Academy of Sciences of the USA.
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- Publisher copy:
- 10.1073/pnas.0700411104
Authors
- Journal:
- Proceedings of the National Academy of Sciences of the United States of America More from this journal
- Volume:
- 104
- Issue:
- 45
- Pages:
- 17662-17667
- Publication date:
- 2007-11-06
- DOI:
- EISSN:
-
1091-6490
- ISSN:
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0027-8424
- Language:
-
English
- Keywords:
- Pubs id:
-
pubs:91024
- UUID:
-
uuid:08e39039-d341-4889-9e3a-a4dc00fffcac
- Local pid:
-
pubs:91024
- Source identifiers:
-
91024
- Deposit date:
-
2012-12-19
- ARK identifier:
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- Copyright date:
- 2007
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