A tilted dataset was collected for rsCSP-Fab667 and rsCSP-Fab668 complexes by changing the stage angle to 0°, -10°, -20°, -30°, -40°, and -50°, resulting in 251 and 505 images, respectively. Particles were picked using DogPicker [49 (link)] and stacked with a box size of 160 or 192 pixels. Micrographs were CTF corrected using GCTF [50 (link)] and particles were extracted. The particle stack was imported into cryoSparc2 [51 (link)], where rounds of reference-free 2D classifications, initial model-free 3D classifications and 3D refinements were performed. 3D refinements did not have symmetry imposed. Crystal structures of Fab667 and 668 were fit to their respective nsEM maps using UCSF Chimera [52 (link)].
Cryo-EM Structure of rsCSP-Fab Complexes
A tilted dataset was collected for rsCSP-Fab667 and rsCSP-Fab668 complexes by changing the stage angle to 0°, -10°, -20°, -30°, -40°, and -50°, resulting in 251 and 505 images, respectively. Particles were picked using DogPicker [49 (link)] and stacked with a box size of 160 or 192 pixels. Micrographs were CTF corrected using GCTF [50 (link)] and particles were extracted. The particle stack was imported into cryoSparc2 [51 (link)], where rounds of reference-free 2D classifications, initial model-free 3D classifications and 3D refinements were performed. 3D refinements did not have symmetry imposed. Crystal structures of Fab667 and 668 were fit to their respective nsEM maps using UCSF Chimera [52 (link)].
Corresponding Organization : Scripps Research Institute
Other organizations : University of California, San Diego, Johns Hopkins University, Kymab (United Kingdom), Itasca Consultants (United States), Wellcome Sanger Institute, Imperial College London
Variable analysis
- Angle of the stage during data collection (0°, -10°, -20°, -30°, -40°, -50°)
- Resulting 251 and 505 images for rsCSP-Fab667 and rsCSP-Fab668 complexes, respectively
- Particle picking and stacking with box sizes of 160 or 192 pixels
- Micrograph CTF correction
- Rounds of reference-free 2D classifications, initial model-free 3D classifications, and 3D refinements in cryoSPARC2
- Fitting of crystal structures of Fab667 and Fab668 to their respective nsEM maps using UCSF Chimera
- Concentration of rsCSP-Fab667 and rsCSP-Fab668 complexes (0.01 mg/ml)
- Buffer used for dilution (1X TBS pH 7.4)
- Negative staining with 2% uranyl formate for 50 seconds
- Microscope used (Thermo Fisher Tecnai Spirit T12 (120 keV) equipped with a TVIPS CMOS 4k x 4k camera)
- Magnification (52,000x)
- Defocus value (-1.5 μm)
- Electron dose (25 e-/Å2)
- Pixel size (2.05 Å)
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