Nature Communications 2015-01-01

Real-time intermembrane force measurements and imaging of lipid domain morphology during hemifusion.

Dong Woog Lee, Kai Kristiansen, Stephen H Donaldson, Nicholas Cadirov, Xavier Banquy, Jacob N Israelachvili

Index: Nat. Commun. 6 , 7238, (2015)

Full Text: HTML

Abstract

Membrane fusion is the core process in membrane trafficking and is essential for cellular transport of proteins and other biomacromolecules. During protein-mediated membrane fusion, membrane proteins are often excluded from the membrane-membrane contact, indicating that local structural transformations in lipid domains play a major role. However, the rearrangements of lipid domains during fusion have not been thoroughly examined. Here using a newly developed Fluorescence Surface Forces Apparatus (FL-SFA), migration of liquid-disordered clusters and depletion of liquid-ordered domains at the membrane-membrane contact are imaged in real time during hemifusion of model lipid membranes, together with simultaneous force-distance and lipid membrane thickness measurements. The load and contact time-dependent hemifusion results show that the domain rearrangements decrease the energy barrier to fusion, illustrating the significance of dynamic domain transformations in membrane fusion processes. Importantly, the FL-SFA can unambiguously correlate interaction forces and in situ imaging in many dynamic interfacial systems.

Related Compounds

Structure Name/CAS No. Articles
Chloroform Structure Chloroform
CAS:67-66-3
Methanol Structure Methanol
CAS:67-56-1
sodium nitrate Structure sodium nitrate
CAS:7631-99-4
1,2-Dipalmitoyl-sn-glycero-3-phosphoethanolamine Structure 1,2-Dipalmitoyl-sn-glycero-3-phosphoethanolamine
CAS:923-61-5