[3dem] LaB6 to cryo - upgrade suggestions

Ludtke, Steven J. sludtke at bcm.edu
Fri Jun 7 13:44:03 PDT 2019


Hi Andrei,
Our core has a 2100 with LAB6 for screening with a DE-12 and a Gatan cryoholder. It is a very nice screening instrument. Potentially good for perhaps 6-10 Å on cryo specimens if everything is optimal, but we generally move to a better instrument as soon as we confirm we have good grids.

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Steven Ludtke, Ph.D. <sludtke at bcm.edu<mailto:sludtke at bcm.edu>>                      Baylor College of Medicine
Charles C. Bell Jr., Professor of Structural Biology
Dept. of Biochemistry and Molecular Biology                      (www.bcm.edu/biochem<http://www.bcm.edu/biochem>)
Academic Director, CryoEM Core                                        (cryoem.bcm.edu<http://cryoem.bcm.edu>)
Co-Director CIBR Center                                    (www.bcm.edu/research/cibr<http://www.bcm.edu/research/cibr>)



On Jun 7, 2019, at 7:25 PM, Andrei Moiseenko <postmoiseenko at gmail.com<mailto:postmoiseenko at gmail.com>> wrote:

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Dear all,
I consider upgrading my microscope to a cryo-em. My purpose is to use it as a screening device and also for low-resolution single particle data acquisition. But I am not sure if our configuration can possibly fit this purpose, so I’m seeking for an advise.
What we already have:
1.       JEOL JEM-2100: 200kV, Cs 1.4, Сс 1.8, LaB6 gun
2.       Anticontaminator: JEOL cryo-fin (not a twin-blade style).
3.       Pretty fine Thon rings up to 5A at -1mkm defocus
4.       Three condenser lenses, nice parallel illumination
5.       Stable 1.0-1.1 eV electron energy spread, measured from EELS ZLP
6.       Already set up single particle acquisition with serialEM for negative stained samples.
What we consider to get:
1.       Direct Electron DE-20 instead of a 2k CCD
2.       Gatan cryo-transfer holder.
I would appreciate any opinion on this upgrade. Does it seem reasonable or not?
I will also be very grateful for any suggestions about highest possible resolution on such a system and about any important limitations that we should be aware of.

Best regards,
Andrey Moiseenko
Electron Microscopy Lab @ Biology Department
Moscow State University
postmoiseenko at gmail.com<mailto:postmoiseenko at gmail.com>
skype: callmoiseenko
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