Séminaire du Prof Alteens - UCL
Nanomechanical Mapping of Virus Binding Sites to Animal Cells
Jeudi 08 mars 2018 à 15h00 – Salle Vésale 030
David Alsteens – Email: david.alsteens@uclouvain.be
Université catholique de Louvain, Croix du sud 4-5, bt L7.07.06, 1348 Louvain-La-Neuve, Belgium
Currently, there is a growing need for methods that can quantify and map the molecular interactions of biological samples, both with high-force sensitivity and high spatial resolution. Force-distance (FD) curve-based atomic force microscopy is a valuable tool to simultaneously contour the surface and map the biophysical properties of biological samples at the nanoscale. We will report the use of advanced FD-based technology combined with chemically functionalized tips to probe the localization and interactions of chemical and biological sites on single native proteins and on living cells at high-resolution. I will present how an atomic force and confocal microscopy set-up allows the surface receptor landscape of cells to be imaged and the virus binding events within the first millisecond of contact with the cell to be mapped at high resolution (<50 nm)1. I will also highlight theoretical approaches to contour the free-energy landscape of early binding events between an engineered virus and cell surface receptors. Owing to its key capabilities (quantitative mapping, resolution of a few nanometers, and true correlation with topography)2-3, this novel biochemically sensitive imaging technique is a powerful complement to other advanced AFM modes for quantitative, high-resolution bioimaging.
Combination of AFM and fluorescence microscopy to map vírus binding sites on living mammalian cells
References:
[1] D. Alsteens et al. Nat. Nanotechnol. 12 (2017) 177-183.
[2] D. Alsteens et al. Nat. Rev. Materials 2 (2017) 17008.
[3] D. Alsteens et al. Nat. Methods 12 (2015) 845-851.
