TY - JOUR
T1 - Sample deposition onto cryo-EM grids
T2 - From sprays to jets and back
AU - Klebl, David P.
AU - Monteiro, Diana C. F.
AU - Kontziampasis, Dimitrios
AU - Kopf, Florian
AU - Sobott, Frank
AU - White, Howard D.
AU - Trebbin, Martin
AU - Muench, Stephen P.
N1 - Funding Information:
We kindly thank Dr Guido Meier for granting us access to the laser lithography instrument and Dr Elena Konig for help with the instrument. All EM data were collected at the Astbury Biostructure Laboratory and we thank the support scientists for their help in data collection setup. The following funding is acknowledged: American Heart Association (grant No. AMR21-236078 to Howard D. White); National Institutes of Health (grant No. 171261 to Howard D. White); Biotechnology and Biological Sciences Research Council (grant No. BB/P026397/1 to Stephen P. Muench); Wellcome Trust (grant No. 108466/Z/15/Z); Bundesminis-terium für Bildung und Forschung (grant No. 05K16GUI to Martin Trebbin); Deutsche Forschungsgemeinschaft [grant No. EX-1074 (194651731) to Martin Trebbin].
Copyright:
© Klebl et al. 2020.
PY - 2020/4/1
Y1 - 2020/4/1
N2 - Despite the great strides made in the field of single-particle cryogenic electron microscopy (cryo-EM) in microscope design, direct electron detectors and new processing suites, the area of sample preparation is still far from ideal. Traditionally, sample preparation involves blotting, which has been used to achieve high resolution, particularly for well behaved samples such as apoferritin. However, this approach is flawed since the blotting process can have adverse effects on some proteins and protein complexes, and the long blot time increases exposure to the damaging air-water interface. To overcome these problems, new blotless approaches have been designed for the direct deposition of the sample on the grid. Here, different methods of producing droplets for sample deposition are compared. Using gas dynamic virtual nozzles, small and high-velocity droplets were deposited on cryo-EM grids, which spread sufficiently for high-resolution cryo-EM imaging. For those wishing to pursue a similar approach, an overview is given of the current use of spray technology for cryo-EM grid preparation and areas for enhancement are pointed out. It is further shown how the broad aspects of sprayer design and operation conditions can be utilized to improve grid quality reproducibly.
AB - Despite the great strides made in the field of single-particle cryogenic electron microscopy (cryo-EM) in microscope design, direct electron detectors and new processing suites, the area of sample preparation is still far from ideal. Traditionally, sample preparation involves blotting, which has been used to achieve high resolution, particularly for well behaved samples such as apoferritin. However, this approach is flawed since the blotting process can have adverse effects on some proteins and protein complexes, and the long blot time increases exposure to the damaging air-water interface. To overcome these problems, new blotless approaches have been designed for the direct deposition of the sample on the grid. Here, different methods of producing droplets for sample deposition are compared. Using gas dynamic virtual nozzles, small and high-velocity droplets were deposited on cryo-EM grids, which spread sufficiently for high-resolution cryo-EM imaging. For those wishing to pursue a similar approach, an overview is given of the current use of spray technology for cryo-EM grid preparation and areas for enhancement are pointed out. It is further shown how the broad aspects of sprayer design and operation conditions can be utilized to improve grid quality reproducibly.
KW - cryo-EM
KW - gas dynamic virtual nozzle
KW - microfluidics
KW - sample preparation
KW - structure determination
KW - time-resolved
UR - http://www.scopus.com/inward/record.url?scp=85083072154&partnerID=8YFLogxK
U2 - 10.1107/S2059798320002958
DO - 10.1107/S2059798320002958
M3 - Article
C2 - 32254058
AN - SCOPUS:85083072154
SN - 2059-7983
VL - D76
SP - 340
EP - 349
JO - Acta Crystallographica Section D: Structural Biology
JF - Acta Crystallographica Section D: Structural Biology
IS - Part 4
ER -