Where in the cell is my protein?. (21st June 2021)
- Record Type:
- Journal Article
- Title:
- Where in the cell is my protein?. (21st June 2021)
- Main Title:
- Where in the cell is my protein?
- Authors:
- DeRosier, David J.
- Abstract:
- Abstract: The application of cryo-correlative light and cryo-electron microscopy (cryo-CLEM) gives us a way to locate structures of interest in the electron microscope. In brief, the structures of interest are fluorescently tagged, and images from the cryo-fluorescent microscope (cryo-FM) maps are superimposed on those from the cryo-electron microscope (cryo-EM). By enhancing cryo-FM to include single-molecule localization microscopy (SMLM), we can achieve much better localization. The introduction of cryo-SMLM increased the yield of photons from fluorophores, which can benefit localization efforts. Dahlberg and Moerner (2021, Annual Review of Physical Chemistry, 72, 253–278) have a recent broad and elegant review of super-resolution cryo-CLEM. This paper focuses on cryo(F)PALM/STORM for the cryo-electron tomography community. I explore the current challenges to increase the accuracy of localization by SMLM and the mapping of those positions onto cryo-EM images and maps. There is much to consider: we need to know if the excitation of fluorophores damages the structures we seek to visualize. We need to determine if higher numerical aperture (NA) objectives, which add complexity to image analysis but increase resolution and the efficiency of photon collection, are better than lower NA objectives, which pose fewer problems. We need to figure out the best way to determine the axial position of fluorophores. We need to have better ways of aligning maps determined by FM with thoseAbstract: The application of cryo-correlative light and cryo-electron microscopy (cryo-CLEM) gives us a way to locate structures of interest in the electron microscope. In brief, the structures of interest are fluorescently tagged, and images from the cryo-fluorescent microscope (cryo-FM) maps are superimposed on those from the cryo-electron microscope (cryo-EM). By enhancing cryo-FM to include single-molecule localization microscopy (SMLM), we can achieve much better localization. The introduction of cryo-SMLM increased the yield of photons from fluorophores, which can benefit localization efforts. Dahlberg and Moerner (2021, Annual Review of Physical Chemistry, 72, 253–278) have a recent broad and elegant review of super-resolution cryo-CLEM. This paper focuses on cryo(F)PALM/STORM for the cryo-electron tomography community. I explore the current challenges to increase the accuracy of localization by SMLM and the mapping of those positions onto cryo-EM images and maps. There is much to consider: we need to know if the excitation of fluorophores damages the structures we seek to visualize. We need to determine if higher numerical aperture (NA) objectives, which add complexity to image analysis but increase resolution and the efficiency of photon collection, are better than lower NA objectives, which pose fewer problems. We need to figure out the best way to determine the axial position of fluorophores. We need to have better ways of aligning maps determined by FM with those determined by EM. We need to improve the instrumentation to be easier to use, more accurate, and ice-contamination free. The bottom line is that we have more work to do. … (more)
- Is Part Of:
- Quarterly reviews of biophysics. Volume 54(2021)
- Journal:
- Quarterly reviews of biophysics
- Issue:
- Volume 54(2021)
- Issue Display:
- Volume 54, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 54
- Issue:
- 2021
- Issue Sort Value:
- 2021-0054-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-06-21
- Subjects:
- Cryo-CLEM -- cryo-electron microscopy -- cryo-ET -- cryo-superresolution fluorescence microscopy -- FIB-SEM microscopy -- localization of structures
Biophysics -- Periodicals
571.405 - Journal URLs:
- http://journals.cambridge.org/action/displayJournal?jid=QRB ↗
- DOI:
- 10.1017/S003358352100007X ↗
- Languages:
- English
- ISSNs:
- 0033-5835
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library HMNTS - ELD Digital store
- Ingest File:
- 18298.xml