Skip to main content
. Author manuscript; available in PMC: 2019 Jan 1.
Published in final edited form as: Methods Mol Biol. 2018;1836:261–279. doi: 10.1007/978-1-4939-8678-1_13

Table 2.

Quantification of influenza virus-liposome contacts, modified from [11].

HA Bridging Pinching Extended Interface Hemifusion Postfusion
Target Membrane Not significantly deformed Pinched and drawn to the virus envelope Running parallel with the virus envelope. Proximal leaflets may be indistinguishable Two proximal leaflets of lipid bilayers have joined and a diaphragm is composed of only the two remaining leaflets Already merged with the virus envelope
HA HAs bridge virus and liposome membrane HAs form a fringe around the dimple No density of HA can be observed at the contact sites No density of HA can be observed at the contact sites HA can adopt a variety of different conformations on the fused surface
Width of Contacts Several to 100 nm < 10 nm 10 – 100 nm ~100 nm The fused complexes may grow up to 500 nm
Internal Features Virus and liposome have not fused Virus and liposome have not fused Virus and liposome have not fused No matrix layer is present and dense clumps formed by M1 and ribonucleoprotein are observed Internal vesicles originate from multi-lamellar liposomes and dense clumps are formed by M1 and ribonucleoprotein
Example Figure 5A Figure 5B Figure 5C Figure 5D Figure 5E