Optical Sciences

Biomolecules and nanostructures

The Optical Sciences group studies the interaction of light and matter at the nanoscale. We do this by exploring ways to shape light and its environment. It's what we call active and passive control. Our current focus is on the interaction of light with biomolecules and nanostructures. We are part of Twente University's Department of Science and Technology and member of the MESA+ institute.
We participate in the EU-COST actions MP1102: Coherent Raman microscopy (MicroCor) and CM1202: Supramolecular photocatalytic water splitting (PERSPECT-H2O)

 

Nanometer-scale organization of the alpha subunits of the receptors for IL2 and IL15 in human T lymphoma cells

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Bärbel I. de Bakker, Andrea Bodnár, Erik M. H. P. van Dijk, György Vámosi, Sándor Damjanovich, Thomas A. Waldmann, Niek F. van Hulst, Attila Jenei, and María F. Garcia-Parajo
Journal of Cell Science
vol 121 issue 5 p627-633 feb 20 2008
doi:10.1242/jcs.019513

Interleukin 2 and interleukin 15 (IL2 and IL15, respectively) provide quite distinct contributions to T-cell-mediated immunity, despite having similar receptor composition and signaling machinery. As most of the proposed mechanisms underlying this apparent paradox attribute key significance to the individual α-chains of IL2 and IL15 receptors, we investigated the spatial organization of the receptors IL2Rα and IL15Rα at the nanometer scale expressed on a human CD4+ leukemia T cell line using single-molecule-sensitive near-field scanning optical microscopy (NSOM). In agreement with previous findings, we here confirm clustering of IL2Rα and IL15Rα at the submicron scale. In addition to clustering, our single-molecule data reveal that a non-negligible percentage of the receptors are organized as monomers. Only a minor fraction of IL2Rα molecules reside outside the clustered domains, whereas ~30% of IL15Rα molecules organize as monomers or small clusters, excluded from the main domain regions.
Interestingly, we also found that the packing densities per unit area of both IL2Rα and IL15Rα domains remained constant, suggesting a ‘building block’ type of assembly involving repeated structures and composition. Finally, dual-color NSOM demonstrated co-clustering of the two α-chains. Our results should aid understanding the action of the IL2R-IL15R system in T cell function and also might contribute to the more rationale design of IL2R- or IL15R-targeted immunotherapy agents for treating human leukemia.
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