Probing single protein dynamics on liposome surfaces
It is crucial to measure position and conformational changes of a membrane-interacting protein relative to the membrane surface. This is however challenging because the thickness of a membrane is usually only about 4 nm. We developed a fluorescence method which makes use of the principle of FRET between a fluorophore and a cloud of quenchers encapsulated in a liposome, hence the name LipoFRET. LipoFRET can readily locate a fluorophore in different depths inside and at different heights above the membrane. We applied LipoFRET to study α-synuclein, a key player in the pathology of Parkinson's disease. Our approach yielded quantita-tive information about the dynamics of different regions of α-syn in lipid membranes, which has never been explored before.