Interferometric fluorescent super-resolution microscopy resolves 3D cellular ultrastructure
Howard Hughes Medical Institute · Janelia Research Campus · +7 more institutions
Abstract
Understanding molecular-scale architecture of cells requires determination of 3D locations of specific proteins with accuracy matching their nanometer-length scale. Existing electron and light microscopy techniques are limited either in molecular specificity or resolution. Here, we introduce interferometric photoactivated localization microscopy (iPALM), the combination of photoactivated localization microscopy with single-photon, simultaneous multiphase interferometry that provides sub-20-nm 3D protein localization with optimal molecular specificity. We demonstrate measurement of the 25-nm microtubule diameter, resolve the dorsal and ventral plasma membranes, and visualize the arrangement of integrin…
Citation impact
- FWCI
- 77.74
- Percentile
- 100%
- References
- 34
Authors
12- GSGleb ShtengelCorresponding
Howard Hughes Medical Institute, Janelia Research Campus
- JAJames A. Galbraith
National Institute of Neurological Disorders and Stroke
- CGCatherine G. Galbraith
National Institute of Dental and Craniofacial Research
- JLJennifer Lippincott‐Schwartz
Health and Human Development (2HD) Research Network
- JMJennifer M. Gillette
Health and Human Development (2HD) Research Network
Topics & keywords
- Microscopy
- Electron microscope
- Resolution (logic)
- Super-resolution microscopy
- Fluorescence microscope
- Endoplasmic reticulum
- Biophysics
- Ultrastructure