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“Introduction The atomic force microscope (AFM), with its picoNewton force sensitivity and AZD3965 nanometer

spatial resolution, provides a powerful tool for exploring intermolecular forces at the single-molecule level and for mapping the topography and organisation of membrane proteins under physiological conditions (Fotiadis et al. 2002; Müller and Dufrêne 2008). AFM studies BVD-523 cell line of bacterial photosynthetic membranes have revealed the membrane organisation of light-harvesting and reaction centre complexes (Scheuring et al. 2007; Sturgis et al. 2009), but this study was made possible by prior knowledge of the structures of these complexes, which made their identification relatively straightforward. However, a different

approach is needed in the absence of reliable structural information and a combination of topographical and functional AFM imaging can circumvent this ‘recognition’ problem, most notably the PicoTREC work (combining topography and antibody-mediated protein recognition) of Hinterdorfer and co-workers (Ebner et al. 2005; Hinterdorfer and Dufrêne 2006; Chtcheglova et al. 2007) and force–volume imaging (Ludwig et al. 1997). Both methods have advantages and drawbacks; the former method lacks high time resolution, thus rendering dynamic

processes effectively invisible, the latter method is reliant upon an antibody (which can be highly variable for polyclonal antibodies) to reliably recognise an antigenic motif and it also cannot quantitatively measure the interaction forces. Here, we present an imaging approach that relies upon a native protein–protein interaction found in bacterial photosynthesis, in this case the reversible binding of an extrinsic cytochrome, (cyt) c 2, to its intrinsic Phosphoprotein phosphatase membrane partner, the photosynthetic reaction centre-light-harvesting 1-PufX (RC-LH1-PufX) complex. This AFM-based imaging method is able to map the location of surface-attached RC-LH1-PufX complexes and to measure the interaction forces involved. Cyclic photosynthetic electron transfer involves the light-induced transfer of electrons from the primary electron donor, a specialised bacteriochlorophyll dimer within the reaction centre (RC), through a series of electron acceptors to reduce a reversibly bound secondary quinone acceptor QB.