TY - JOUR
T1 - Vitrification of thick samples for soft X-ray cryo-tomography by high pressure freezing
AU - Weiner, Allon
AU - Kapishnikov, Sergey
AU - Shimoni, Eyal
AU - Cordes, Sandra
AU - Guttmann, Peter
AU - Schneider, Gerd
AU - Elbaum, Michael
N1 - Funding Information: The authors thank Lothar Houben for discussions on tomographic reconstruction and its evaluation. Protocol developments were conducted at the Irving and Cherna Moscowitz Center for Nano and Bio-nano Imaging of the Weizmann Institute of Science. This work was supported in part by the Minerva Research Foundation, the Helen and Milton A. Kimmelman Center for Biological Structure and Assembly, the Gerhardt M.J. Schmidt Minerva Center for Supramolecular Architecture, and the Clore Center for Biological Physics. AW acknowledges receipt of the Curwen-Lowy Fellowship. We have benefited as well from the historical generosity of the Harold Perlman family. We acknowledge the Helmholtz-Zentrum Berlin - Electron storage ring BESSY II for provision of synchrotron radiation at beamline U41, with funding from the European Community’s Seventh Framework Programme ( FP7/2007-2013 ) under grant agreement no. 226716 .
PY - 2013/1
Y1 - 2013/1
N2 - Soft X-ray cryo-microscopy (cryo-XT) offers an ideal complement to electron cryo-microscopy (cryo-EM). Cryo-XT is applicable to samples more than an order of magnitude thicker than cryo-EM, albeit at a more modest resolution of tens of nanometers. Furthermore, the natural contrast obtained in the "water-window" by differential absorption by organic matter vs water yields detailed images of organelles, membranes, protein complexes, and other cellular components. Cryo-XT is thus ideally suited for tomography of eukaryotic cells. The increase in sample thickness places more stringent demands on sample preparation, however. The standard method for cryo-EM, i.e., plunging to a cryogenic fluid such as liquid ethane, is no longer ideally suited to obtain vitrification of thick samples for cryo-XT. High pressure freezing is an alternative approach, most closely associated with freeze-substitution and embedding, or with electron cryo-microscopy of vitreous sections (CEMOVIS). We show here that high pressure freezing can be adapted to soft X-ray tomography of whole vitrified samples, yielding a highly reliable method that avoids crystallization artifacts and potentially offers improved imaging conditions in samples not amenable to plunge-freezing.
AB - Soft X-ray cryo-microscopy (cryo-XT) offers an ideal complement to electron cryo-microscopy (cryo-EM). Cryo-XT is applicable to samples more than an order of magnitude thicker than cryo-EM, albeit at a more modest resolution of tens of nanometers. Furthermore, the natural contrast obtained in the "water-window" by differential absorption by organic matter vs water yields detailed images of organelles, membranes, protein complexes, and other cellular components. Cryo-XT is thus ideally suited for tomography of eukaryotic cells. The increase in sample thickness places more stringent demands on sample preparation, however. The standard method for cryo-EM, i.e., plunging to a cryogenic fluid such as liquid ethane, is no longer ideally suited to obtain vitrification of thick samples for cryo-XT. High pressure freezing is an alternative approach, most closely associated with freeze-substitution and embedding, or with electron cryo-microscopy of vitreous sections (CEMOVIS). We show here that high pressure freezing can be adapted to soft X-ray tomography of whole vitrified samples, yielding a highly reliable method that avoids crystallization artifacts and potentially offers improved imaging conditions in samples not amenable to plunge-freezing.
KW - Electron cryo-microscopy
KW - High pressure freezing
KW - Plasmodium
KW - Tomography
KW - Water-window
KW - X-ray microscopy
UR - https://www.scopus.com/pages/publications/84870894574
U2 - 10.1016/j.jsb.2012.10.005
DO - 10.1016/j.jsb.2012.10.005
M3 - Article
C2 - 23079478
SN - 1047-8477
VL - 181
SP - 77
EP - 81
JO - Journal of Structural Biology
JF - Journal of Structural Biology
IS - 1
ER -