Abstract:
:Electron cryo-tomography (cryoET) is currently the only technique that allows the direct observation of proteins in their native cellular environment. Sub-volume averaging of electron tomograms offers a route to increase the signal-to-noise of repetitive biological structures, such improving the information content and interpretability of tomograms. We discuss the potential for sub-volume averaging in highlighting and investigating specific processes in situ, focusing on microtubule structure and viral infection. We show that (i) in situ sub-volume averaging from single tomograms can guide and complement segmentation of biological features, (ii) the in situ determination of the structure of individual viruses is possible as they infect a cell, and (iii) novel, transient processes can be imaged with high levels of detail.
journal_name
J Struct Bioljournal_title
Journal of structural biologyauthors
Grange M,Vasishtan D,Grünewald Kdoi
10.1016/j.jsb.2016.06.024subject
Has Abstractpub_date
2017-02-01 00:00:00pages
181-190issue
2eissn
1047-8477issn
1095-8657pii
S1047-8477(16)30139-3journal_volume
197pub_type
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