(2.5pmol) in DNA binding buffer +/− 1mM AMP-PNP. For PAXX samples,
7.5pmol of PAXX was included. Complexes were equilibrated on ice for 15 min.,
diluted 1:5 with DNA binding buffer and immediately 3μL of sample applied
to a glow-discharged carbon film 400 mesh copper grid (Electron Microscopy
Sciences, Hatfield PA). The sample was washed twice with water, then stained
with 2% uranyl acetate. Excess stain was blotted off and the grids allowed to
dry before imaging on 120kV Talos microscope with a BM-Ceta camera (Thermo
Scientific).