TY - JOUR
T1 - Advances in tomography
T2 - Probing the molecular architecture of cells
AU - Fridman, Karen
AU - Mader, Asaf
AU - Zwerger, Monika
AU - Elia, Natalie
AU - Medalia, Ohad
N1 - Funding Information:
The authors work is supported by the Swiss National Science Foundation (SNSF), the National Center for Competence in Research in Structural Biology, a Swiss National Science Foundation grant (SNSF 31003A_141083/1) and an European Research Council (ERC) Starting Grant (243047 INCEL).
PY - 2012/11/1
Y1 - 2012/11/1
N2 - Visualizing the dynamic molecular architecture of cells is instrumental for answering fundamental questions in cellular and structural biology. Although modern microscopy techniques, including fluorescence and conventional electron microscopy, have allowed us to gain insights into the molecular organization of cells, they are limited in their ability to visualize multicomponent complexes in their native environment. Cryo-electron tomography (cryo-ET) allows cells, and the macromolecular assemblies contained within, to be reconstructed in situ, at a resolution of 2-6 nm. By combining cryo-ET with super-resolution fluorescence microscopy approaches, it should be possible to localize proteins with high precision inside cells and so elucidate a more realistic view of cellular processes. Thus, cryo-ET may bridge the resolution gap between cellular and structural biology.
AB - Visualizing the dynamic molecular architecture of cells is instrumental for answering fundamental questions in cellular and structural biology. Although modern microscopy techniques, including fluorescence and conventional electron microscopy, have allowed us to gain insights into the molecular organization of cells, they are limited in their ability to visualize multicomponent complexes in their native environment. Cryo-electron tomography (cryo-ET) allows cells, and the macromolecular assemblies contained within, to be reconstructed in situ, at a resolution of 2-6 nm. By combining cryo-ET with super-resolution fluorescence microscopy approaches, it should be possible to localize proteins with high precision inside cells and so elucidate a more realistic view of cellular processes. Thus, cryo-ET may bridge the resolution gap between cellular and structural biology.
UR - http://www.scopus.com/inward/record.url?scp=84867870229&partnerID=8YFLogxK
U2 - 10.1038/nrm3453
DO - 10.1038/nrm3453
M3 - Review article
C2 - 23047735
AN - SCOPUS:84867870229
SN - 1471-0072
VL - 13
SP - 736
EP - 742
JO - Nature Reviews Molecular Cell Biology
JF - Nature Reviews Molecular Cell Biology
IS - 11
ER -