A permissive geometry model for TCR–CD3 activation
Trends in Biochemical Sciences, ISSN: 0968-0004, Vol: 33, Issue: 2, Page: 51-57
2008
- 38Citations
- 55Captures
- 1Mentions
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations38
- Citation Indexes38
- 38
- CrossRef36
- Captures55
- Readers55
- 55
- Mentions1
- References1
- Wikipedia1
Article Description
The T cell antigen receptor (TCR–CD3) is the most complex receptor known to date, consisting of eight transmembrane subunits. Its activation by an antigen is the initial step in an immune response. Here, we present the permissive geometry model explaining how antigen binding initiates intracellular signalling cascades. We propose that a dimeric antigen imposes its geometry on two TCR–CD3 receptors by simultaneously binding to both. This causes the TCRαβ subunits to rotate with respect to each other leading to displacement of the ectodomains of the associated CD3 dimers. This results in a scissor-like movement of the CD3 dimers that opens the cytoplasmic tails for interaction with signalling proteins, thus initiating signalling cascades.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0968000408000029; http://dx.doi.org/10.1016/j.tibs.2007.10.008; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=38949089676&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/18201888; https://linkinghub.elsevier.com/retrieve/pii/S0968000408000029
Elsevier BV
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