To date the fields of biophysics, biochemistry, molecular and cellular biology and have established exhaustive correlations between the lipid composition of membranes and its impact on membrane properties and protein function. However, in addition to composition the shape of cellular membranes appears to be a well-conserved phenotype in evolution. The characteristic membrane topology of organelles e.g. the folded structure of the endoplasmatic reticulum, is strictly retained in most types of cells. Nevertheless we largely ignore what are the consequences of membrane shape/curvature to biological functions that make it so critical for sustaining life. The lack of information on the significance of membrane shape has predominantly been due to the absence of reliable assays that allow us to perform systematic experiments as a function of membrane shape/curvature. We have recently demonstrated the possibility to construct a high throughput array of unique nanoscale membrane curvatures. The assay is based on unilamellar liposomes of different diameters (30 nm to 700 nm), and therefore curvature, that are immobilized on a surface at dilute densities allowing for imaging of single liposomes with fluorescence microscopy.Here I will discuss published and unpublished data on two important classes of biomolecular interactions that exhibited dramatic curvature dependence: i) SNARE-mediated docking of single lipid vesicles and ii) membrane anchoring of lipidated proteins, and reveal previously unsuspected consequences of membrane curvature to biological function.
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