Cryo-EM
May. 20, 2010
Numerous cells in our bodies are capable of active movement. They use an internal "motor" coupled with a cunning recycling system. Researchers from IMBA (Institute of Molecular Biotechnology) and IMP (Institute of Molecular Pathology) in Vienna, Austria have been able to literally freeze this process using cryo-electron tomography and to get a truthful picture of the cell's internal propulsion system. Their findings, which challenge existing textbook models, make the cover-story of the May issue of the journal Nature Cell Biology.
moreMay. 17, 2010
UCLA researchers (USA) report in the journal Cell that they have imaged a virus structure at a resolution high enough to effectively "see" atoms, the first published instance of imaging biological complexes at such a resolution. The research team, led by Hong Zhou, UCLA professor of microbiology, immunology and molecular genetics, used cryo-electron microscopy to image the structure at 3.3 angstroms. An angstrom is the smallest recognized division of a chemical element and is about the distance between the two hydrogen atoms in a water molecule.
moreMay. 05, 2010
UCLA researchers (USA) report in the journal Cell that they have imaged a virus structure at a resolution high enough to effectively "see" atoms, the first published instance of imaging biological complexes at such a resolution. The research team, led by Hong Zhou, UCLA professor of microbiology, immunology and molecular genetics, used cryo-electron microscopy to image the structure at 3.3 angstroms. An angstrom is the smallest recognized division of a chemical element and is about the distance between the two hydrogen atoms in a water molecule.
moreNov. 01, 2007
Cryo-fluorescence Microscopy. The use of a novel cryo-light microscope stage enabled C. Schwartz and her colleagues to perform correlative light and electron microscopy of vitreous samples prepared for cryo-EM. In addition to the correlative imaging aspect, photobleaching of the fluorophores is reduced the cryogenic temperatures (-140 °C) of the setup.
J. Microsc., 227, pp. 98-109
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