Transmission electron cryomicroscopy(Redirected from Cryoelectron microscopy)
Transmission electron cryomicroscopy (CryoTEM), commonly known as cryo-EM, is a form of cryogenic electron microscopy, more specifically a type of transmission electron microscopy (TEM) where the sample is studied at cryogenic temperatures (generally liquid-nitrogen temperatures). Cryo-EM is gaining popularity in structural biology.
The utility of transmission electron cryomicroscopy stems from the fact that it allows the observation of specimens that have not been stained or fixed in any way, showing them in their native environment. This is in contrast to X-ray crystallography, which requires crystallizing the specimen, which can be difficult, and placing them in non-physiological environments, which can occasionally lead to functionally irrelevant conformational changes.
Recent advances in detector technology and software algorithms have allowed for the determination of macromolecular structures at near-atomic resolution by cryo-EM. These include viruses, ribosomes, mitochondria, ion channels, and enzyme complexes. As of 2018, cryo-EM can be applied to structures as small as hemoglobin (64 kDa) and with resolutions up to 1.8 Å. Cryo-EM structures currently represent just under 2% of structures deposited in the Protein Data Bank, although this number is rapidly increasing as more and more cryo-EM structures are published each year. An application of cryo-EM is cryo-electron tomography (cryo-ET), where a 3D reconstruction of the sample is created from tilted 2D images.
The original rationale for CryoTEM was as a means to fight radiation damage for biological specimens. The amount of radiation required to collect an image of a specimen in the electron microscope is high enough to be a potential source of specimen damage for delicate structures. In addition, the high vacuum required on the column of an electron microscope makes the environment for the sample quite harsh.
The problem of the vacuum was partially solved by the introduction of negative stains but even with negative stains biological samples are prone to structural collapse upon dehydration of the specimen. Embedding the samples in ice below the sublimation temperature was a possibility that was contemplated early on, but water tends to arrange into a crystalline lattice of lower density upon freezing and this can destroy the structure of anything that is embedded in it.
In the early 1980s, several groups studying solid state physics were attempting to produce vitreous ice by different means, such as high pressure freezing or flash freezing. In a seminal paper in 1984, the group led by Jacques Dubochet at the European Molecular Biology Laboratory showed images of adenovirus embedded in a vitrified layer of water. This paper is generally considered to mark the origin of Cryo-EM, and the technique has been developed to the point of becoming routine at numerous laboratories throughout the world.
The energy of the electrons used for imaging (80-300 kV) is high enough that covalent bonds can be broken. When imaging specimens vulnerable to radiation damage, it is necessary to limit the electron exposure used to acquire the image. These low exposures require that the images of thousands or even millions of identical frozen molecules be selected, aligned, and averaged to obtain high-resolution maps, using specialized software. A significant improvement in structural features was achieved in 2012 by the introduction of direct electron detectors and better computational algorithms.
In 2015, Bridget Carragher and colleagues at the Scripps National Resource for Automated Molecular Microscopy used techniques she and Clint Potter developed to determine the first cryo-EM structure with a resolution finer than 3 Å, thereby elevating CryoTEM as a tool comparable to and potentially superior to traditional x-ray crystallography techniques. Since then, higher resolutions have been achieved, including a 2.2 Å structure of bacterial enzyme β-galactosidase in 2015 and a 1.8 Å structure of glutamate dehydrogenase in 2016. Cryo-EM has also been used to determine the structure of various viruses, including the Zika virus, and has been applied to large complexes such as the spliceosome. In 2017, the Nobel Prize in Chemistry was awarded jointly to Jacques Dubochet, Joachim Frank and Richard Henderson, "for developing cryo-electron microscopy for the high-resolution structure determination of biomolecules in solution".
The biological material is spread on an electron microscopy grid and is preserved in a frozen-hydrated state by rapid freezing, usually in liquid ethane near liquid nitrogen temperature. By maintaining specimens at liquid nitrogen temperature or colder, they can be introduced into the high-vacuum of the electron microscope column. Most biological specimens are extremely radiosensitive, so they must be imaged with low-dose techniques (usefully, the low temperature of transmission electron cryomicroscopy provides an additional protective factor against radiation damage).
Consequently, the images are extremely noisy. For some biological systems it is possible to average images to increase the signal-to-noise ratio and retrieve high-resolution information about the specimen using the technique known as single particle analysis. This approach in general requires that the things being averaged are identical, although some limited conformational heterogeneity can now be studied (e.g. ribosome). Three-dimensional reconstructions from CryoTEM images of protein complexes and viruses have been solved to sub-nanometer or near-atomic resolution, allowing new insights into the structure and biology of these large assemblies.
Analysis of ordered arrays of protein, such as 2-D crystals of transmembrane proteins or helical arrays of proteins, also allows a kind of averaging which can provide high-resolution information about the specimen. This technique is called electron crystallography.
The thin film method is limited to thin specimens (typically < 500 nm) because the electrons cannot cross thicker samples without multiple scattering events. Thicker specimens can be vitrified by plunge freezing (cryofixation) in ethane (up to tens of μm in thickness) or more commonly by high pressure freezing (up to hundreds of μm). They can then be cut in thin sections (40 to 200 nm thick) with a diamond knife in a cryoultramicrotome at temperatures lower than -135 °C (devitrification temperature). The sections are collected on an electron microscope grid and are imaged in the same manner as specimen vitrified in thin film. This technique is called transmission electron cryomicroscopy of vitreous sections (CEMOVIS) or transmission electron cryomicroscopy of frozen-hydrated sections.
In addition to allowing vitrified biological samples to be imaged, CryoTEM can also be used to image material specimens that are too volatile in vacuum to image using standard, room temperature electron microscopy. For example, vitrified sections of liquid-solid interfaces can be extracted for analysis by CryoTEM, and sulfur, which is prone to sublimation in the vacuum of electron microscopes, can be stabilized and imaged in CryoTEM.
A variety of techniques can be used in CryoTEM. Popular techniques include:
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- Kühlbrandt W (August 2014). "Cryo-EM enters a new era". eLife. 3: e03678. doi:10.7554/elife.03678. PMC 4131193. PMID 25122623.
- Callaway E (September 2015). "The revolution will not be crystallized: a new method sweeps through structural biology". Nature. 525 (7568): 172–4. Bibcode:2015Natur.525..172C. doi:10.1038/525172a. PMID 26354465.
- Khoshouei M, Radjainia M, Baumeister W, Danev R (June 2017). "Cryo-EM structure of haemoglobin at 3.2 Å determined with the Volta phase plate". Nature Communications. 8: 16099. doi:10.1038/ncomms16099. PMID 28665412.
- Merk A, Bartesaghi A, Banerjee S, Falconieri V, Rao P, Davis MI, Pragani R, Boxer MB, Earl LA, Milne JL, Subramaniam S (June 2016). "Breaking Cryo-EM Resolution Barriers to Facilitate Drug Discovery". Cell. 165 (7): 1698–1707. doi:10.1016/j.cell.2016.05.040. PMID 27238019.
- "PDB Data Distribution by Experimental Method and Molecular Type". www.rcsb.org. Retrieved 2018-12-22.
- "PDB Statistics: Growth of Structures from 3DEM Experiments Released per Year". www.rcsb.org. Retrieved 2018-12-22.
- Adrian M, Dubochet J, Lepault J, McDowall AW (1984). "Cryo-electron microscopy of viruses". Nature. 308 (5954): 32–6. Bibcode:1984Natur.308...32A. doi:10.1038/308032a0. PMID 6322001.
- Dellisanti, Cosma (2015). "A barrier-breaking resolution". Nature Structural & Molecular Biology. 22 (5): 361. doi:10.1038/nsmb.3025.
- Campbell MG, Veesler D, Cheng A, Potter CS, Carragher B (March 2015). "2.8 Å resolution reconstruction of the Thermoplasma acidophilum 20S proteasome using cryo-electron microscopy". eLife. 4. doi:10.7554/eLife.06380. PMC 4391500. PMID 25760083.
- Bartesaghi A, Merk A, Banerjee S, Matthies D, Wu X, Milne JL, Subramaniam S (June 2015). "2.2 Å resolution cryo-EM structure of β-galactosidase in complex with a cell-permeant inhibitor". Science. 348 (6239): 1147–51. doi:10.1126/science.aab1576. PMID 25953817.
- Vonck J, Mills DJ (October 2017). "Advances in high-resolution cryo-EM of oligomeric enzymes". Current Opinion in Structural Biology. 46: 48–54. doi:10.1016/j.sbi.2017.05.016. PMID 28624735.
- Sirohi D, Chen Z, Sun L, Klose T, Pierson TC, Rossmann MG, Kuhn RJ (April 2016). "The 3.8 Å resolution cryo-EM structure of Zika virus". Science. 352 (6284): 467–70. doi:10.1126/science.aaf5316. PMC 4845755. PMID 27033547.
- Cheng Y (August 2018). "Single-particle cryo-EM-How did it get here and where will it go". Science. 361 (6405): 876–880. doi:10.1126/science.aat4346. PMID 30166484.
- "The 2017 Nobel Prize in Chemistry - Press Release". www.nobelprize.org. 4 October 2017. Retrieved 4 October 2017.
- Zachman MJ, Asenath-Smith E, Estroff LA, Kourkoutis LF (December 2016). "Site-Specific Preparation of Intact Solid-Liquid Interfaces by Label-Free In Situ Localization and Cryo-Focused Ion Beam Lift-Out". Microscopy and Microanalysis. 22 (6): 1338–1349. Bibcode:2016MiMic..22.1338Z. doi:10.1017/S1431927616011892. PMID 27869059.
- Levin BD, Zachman MJ, Werner JG, Sahore R, Nguyen KX, Han Y, Xie B, Ma L, Archer LA, Giannelis EP, Wiesner U, Kourkoutis LF, Muller DA (February 2017). "Characterization of Sulfur and Nanostructured Sulfur Battery Cathodes in Electron Microscopy Without Sublimation Artifacts". Microscopy and Microanalysis. 23 (1): 155–162. Bibcode:2017MiMic..23..155L. doi:10.1017/S1431927617000058. PMID 28228169.
- Presentation on Cryoelectron Microscopy | PharmaXChange.info
- Shi D, Nannenga BL, Iadanza MG, Gonen T (November 2013). "Three-dimensional electron crystallography of protein microcrystals". eLife. 2: e01345. doi:10.7554/eLife.01345. PMC 3831942. PMID 24252878.
- Nannenga BL, Shi D, Leslie AG, Gonen T (September 2014). "High-resolution structure determination by continuous-rotation data collection in MicroED". Nature Methods. 11 (9): 927–930. doi:10.1038/nmeth.3043. PMC 4149488. PMID 25086503.
- Shi D, Nannenga BL, de la Cruz MJ, Liu J, Sawtelle S, Calero G, Reyes FE, Hattne J, Gonen T (May 2016). "The collection of MicroED data for macromolecular crystallography". Nature Protocols. 11 (5): 895–904. doi:10.1038/nprot.2016.046. PMC 5357465. PMID 27077331.
- de la Cruz MJ, Hattne J, Shi D, Seidler P, Rodriguez J, Reyes FE, Sawaya MR, Cascio D, Weiss SC, Kim SK, Hinck CS, Hinck AP, Calero G, Eisenberg D, Gonen T (February 2017). "Atomic-resolution structures from fragmented protein crystals with the cryoEM method MicroED". Nature Methods. 14 (4): 399–402. doi:10.1038/nmeth.4178. PMC 5376236. PMID 28192420.
- Fu Z, Kaledhonkar S, Borg A, Sun M, Chen B, Grassucci RA, Ehrenberg M, Frank J (December 2016). "Key Intermediates in Ribosome Recycling Visualized by Time-Resolved Cryoelectron Microscopy". Structure. 24 (12): 2092–2101. doi:10.1016/j.str.2016.09.014. PMC 5143168. PMID 27818103.
- Feng X, Fu Z, Kaledhonkar S, Jia Y, Shah B, Jin A, Liu Z, Sun M, Chen B, Grassucci RA, Ren Y, Jiang H, Frank J, Lin Q (April 2017). "A Fast and Effective Microfluidic Spraying-Plunging Method for High-Resolution Single-Particle Cryo-EM". Structure. 25 (4): 663–670.e3. doi:10.1016/j.str.2017.02.005. PMC 5382802. PMID 28286002.
- Chen B, Kaledhonkar S, Sun M, Shen B, Lu Z, Barnard D, Lu TM, Gonzalez RL, Frank J (June 2015). "Structural dynamics of ribosome subunit association studied by mixing-spraying time-resolved cryogenic electron microscopy". Structure. 23 (6): 1097–105. doi:10.1016/j.str.2015.04.007. PMC 4456197. PMID 26004440.
- Frank J (2006). Three-Dimensional Electron Microscopy of Macromolecular Assemblies. New York: Oxford University Press. ISBN 0-19-518218-9.
- van Heel M, Gowen B, Matadeen R, Orlova EV, Finn R, Pape T, Cohen D, Stark H, Schmidt R, Schatz M, Patwardhan A (November 2000). "Single-particle electron cryo-microscopy: towards atomic resolution". Quarterly Reviews of Biophysics. 33 (4): 307–69. doi:10.1017/s0033583500003644. PMID 11233408.
- "EM for Dummies". EM for Dummies. Retrieved June 9, 2006.
- The Fine Structure of a Frozen Virus - Sophisticated single-particle electron cryomicroscopy reveals unprecedented details in a virus's protein coat, Technology Review, March 19, 2008
- Getting Started in Cryo-EM - Online course from Caltech, Professor Grant Jensen
- EM Data Bank
- EMstats Trends and distributions of maps in EMDB, e.g. resolution trends