2018 Vol. 4, No. 3

Cover Story
ATP-binding cassette (ABC) transporters are found in all forms of life from microbes to humans,and transport a wide variety of substrates across the cell membrane using the energy released from ATP hydrolysis and an alternating-access mechanism.MsbA is a homodimeric ABC exporter from Gram-negative bacteria,and transports amphipathic substrates including precursors of lipopolysaccharides from the inner leaflet to the outer leaflet of the cytoplasmic membrane.Despite extensive structural and functional studies,controversies remain regarding the dynamic properties of the conformational changes of MsbA during its transport cycle in the lipid environment.Here,the authors used single-molecule fluorescence resonance energy transfer (smFRET) to explore the dynamic behaviors of MsbA in detergent micelles,nanodiscs,and proteoliposomes.MsbA reconstituted into liposomes showed higher transition frequency between different states on the cytoplasmic side,whereas detergent-solubilized MsbA showed higher transition frequency on the periplasmic side.Three major states were identified from this smFRET study in the functional cycle of MsbA,including an intermediate conformation between the fully opened and fully closed cytoplasmic conformations,associated with both ATP binding and hydrolysis.
Proton transfer during class-A GPCR activation: do the CWxP motif and the membrane potential act in concert?
Evaluation of RNA secondary structure prediction for both base-pairing and topology
Three-dimensional electron spin resonance imaging of endogenous nitric oxide radicals generated in living plants
The application of CorrSightTM in correlative light and electron microscopy of vitrified biological specimens
Single-molecule fluorescence studies on the conformational change of the ABC transporter MsbA