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
Microdomains of the C-type lectin DC-SIGN are portals for virus entry into dendritic cells(full pdf)
Alessandra Cambi, Frank de Lange, Noortje M. van Maarseveen, Monique Nijhuis, Ben Joosten, Erik M.H.P. van Dijk, Bärbel I. de Bakker, Jack A.M. Fransen, Petra H.M. Bovee-Geurts, Frank N. van Leeuwen, Niek F. Van Hulst and Carl G. Figdor
The Journal of Cell Biology
Volume 164, Number 1, 145-155, 5 January 2004
The C-type lectin dendritic cell (DC)-specific intercellular adhesion molecule grabbing non-integrin (DC-SIGN; CD209) facilitates binding and internalization of several viruses, including HIV-1, on DCs, but the underlying mechanism for being such an efficient phagocytic pathogen-recognition receptor is poorly understood. By high resolution electron microscopy, we demonstrate a direct relation between DC-SIGN function as viral receptor and its microlocalization on the plasma membrane. During development of human monocyte-derived DCs, DC-SIGN becomes organized in well-defined microdomains, with an average diameter of 200 nm. Biochemical experiments and confocal microscopy indicate that DC-SIGN microdomains reside within lipid rafts. Finally, we show that the organization of DC-SIGN in microdomains on the plasma membrane is important for binding and internalization of virus particles, suggesting that these multimolecular assemblies of DC-SIGN act as a docking site for pathogens like HIV-1 to invade the host.