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Table 1 Analysis of ASLV-A entry into and fusion with acidic endosomes

From: Pinpointing retrovirus entry sites in cells expressing alternatively spliced receptor isoforms by single virus imaging

Cell lines

Number of EcpH quenching events

EcpH quenching events followed by mKate2 release

% Fused

TVA800

37

11

29.7

TVA950

45

9

20.0

  1. ASLV-A pseudoviruses co-labeled with EcpH-ICAM and Gag-mKate2 were allowed to enter and fuse with TVA800 or TVA950 cells. The number of particles undergoing fusion (mKate2 release) was determined and normalized to the number of particles entering acidic compartments (EcpH quenching).