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Updated: Aug 4, 2025

A TIRF Microscopy Technique for Real-time, Simultaneous Imaging of the TCR and its Associated Signaling Proteins
Published on: March 22, 2012
Imaging the T-cell receptor: new approaches, new insights
Adam M Rochussen1, Anna H Lippert1, Gillian M Griffiths1
1Cambridge Institute for Medical Research, Keith Peters Building, Biomedical Campus, Hills Road, Cambridge CB2 0XY, United Kingdom.
Abstract:
T cells recognize pathogenic antigens via the T-cell antigen receptor (TCR). This protein complex binds to antigen fragments on the surface of antigen-presenting cells. To understand how cellular activation can ensue rapidly from molecular recognition, the localization and distribution of the TCR on the surface of the resting T cell are of particular importance. Conflicting results regarding TCR distribution have emerged from recent studies using a range of imaging techniques, including total internal reflection and single-molecule localization microscopy modalities. Here, we review the differing results and the potential biases inherent in differing imaging approaches. In addition, we review studies showing the impact of differing imaging surfaces on T-cell activation.
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