作者: Stephen ED Webb , Michael Hirsch , Sarah R Needham , Benjamin C Coles , Kathrin M Scherer
DOI: 10.1016/J.YMETH.2015.05.009
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摘要: Although considerable progress has been made in imaging distances cells below the diffraction limit using FRET and super-resolution microscopy, methods for determining separation of macromolecules 10-50 nm range have elusive. We developed fluorophore localisation with photobleaching (FLImP), based on quantised bleaching individual protein-bound dye molecules, to quantitate molecular separations oligomers nanoscale clusters. demonstrate benefits our method studying nanometric organisation epidermal growth factor receptor cells.