Sub-3Å proteasome image-shift data collection¶

This data collection obtained same quality data set as stage shift at 2.5x speed with the same presets. Even more speed gain relative to super-resolution mode data collection.

The speed gain relative to previous stage shift data collection is from

1. removing iterative movement at Exposure node
2. removing queue processing at Exposure node since both need target adjustment and considerable wait time before stable imaging.
3. using counting mode. not super-resolution mode on K2.

VERY IMPORTANT: Measure the amount of beam tilt associated with the image-shift at your scope so that it is not compromising the data. Our scope is at 0.3 mrad at the 1.7 um image shift we applied in this experiment.

The Transfer Function will reduce all structure factor to 78% at these beamtilts assuming 0.167 mrad per 1 um image shift:

image shift (um)	45 degree phase modification resolution(0.78 transfer function amplitude) (Angstroms)
1	2.4
2	3.0
3	3.5
4	3.8

Instruments¶

SEMC@NYSBC Krios

1. Scope: FEI Titan-Krios, 300 kV, micro probe at low mag, nano probe at high mags
2. Camera: Gatan K2. mount below Falcon/Ceta. 1.21 Å at 29kx scope nominal mag

Grid¶

• 1.2/1.3 C-flat carbon support; 400 mesh Copper grid.

Krios-K2 Presets used for 2.8 A proteasome reconstruction in 5 hours data collection at SEMC @ NYSBC¶

• Nanoprobe was used to allow smaller beam to be used for multiple targeting on 2 um hole although not essential in this case.

Tecnai Krios 300 kV high tension, XFEG, Gun Lens 4 extraction voltage 4100, 70 um C2 aperture and 100 um objective aperture (except when obtaining grid atlas).
Gatan camera dimension 3710(w)x 3838(h) after rotation to Leginon standard. The size of the beam on the scope main viewing screen always covers the 1.2 um hole at en preset on our scope.
Pixel size is 1.10 A at 22500x scope nominal mag.:

Probe	Lens Series	Magnification:	Preset name:	Image Shift (x,y):	Dimension:	Binning:	Camera Dose (e/camera pixel/s):	Exposure Time (ms):	Specimen Dose Rate (e/A^2):	Spot Size:	Defocus (m):	C2 (um):	frame saving:	Camera
micro	LM	100	gr	Aligned	1024x1024	4	n/a	500	n/a	5	0.0	70	no	Ceta
micro	SA	400**	sq	Aligned	927x959	4	8	100	n/a	10	-2e-4	70	no	K2
nano	SA	1300**	hl	Aligned	927x959	4	8	200	0.004	11	-1.5e-4	70	no	K2
nano	SA	22500	fc	0,0	924x924	2	>=8*	500	3.3	8	-7e-7	70	no	K2
nano	SA	22500	fa	0,0	927x959	4	>=8*	250	1.65	8	-1.5e-6	70	no	K2
nano	SA	22500	en	0,0	3710x3838	1	8 e/pixel/s and ~0.7 um on the specimen	7000	46	8	(-1e-6 to -2e-6)	70	200 ms/frame

**These two magnifications are add-on to standard SA lens series made for NYSBC Krios1. May not be available at other scopes.

• Note: If the correlation or power spectrum don't work well enough for the standard Camera Dose Rate of 10 e/pixel/s for fc and fa, you may increase it more so not to have to use longer exposure time. The recommended value in literature is meant to give highest DQE at all sampling frequencies. Using a higher camera dose by 50% will certainly not damage the sensor.

• Note: no defocal pair was acquired in this experiment. Therefore, no ef preset.

Application:¶

MSI-T2 Advanced (= MSI-T + "Beam Tilt Image" for coma-free alignment + "N2 Filling" for Krios auto nitrogen filler)

Presets Manager:¶

No preset cycling (Krios has its own normalization).

Queuing usage:¶

Hole Targeting: Queuing, target at the carbon area to cover four holes.
Exposure Targeting: No Queuing. automated targeting. See Exposure Targeting Set-up for MSi-T for Four Holes

Move method to reach the targets:¶

Hole: Navigator Iterative movement: Target Tolerance: 1e-7 m; Acceptable Tolerance: 3e-7 m
Focus: Presets Manager image shift
Exposure: Presets Manager image shift

Wait time before final exposure:
3 seconds
10 seconds addition for the first target¶