Imaging Intracellular Fluorescent Proteins at Nanometer Resolution
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Summary
This work introduced a method for optically imaging intracellular proteins at nanometer spatial resolution and used this method to image specific target proteins in thin sections of lysosomes and mitochondria and in fixed whole cells to image retroviral protein Gag at the plasma membrane.
- Type
- article
- Published
- 2006-09-15
- Cited by
- 8,457
- References
- 42
- OpenAlex
- https://openalex.org/W2054455698
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:807611
Keywords
Vinculin, Lamellipodium, Microscopy, Actin, Superresolution
References
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- An epidemic of complex dysmorphologic syndromes in southeast Spain?
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Cited by
- Chapter 12: Nanoscale biological fluorescence imaging: breaking the diffraction barrier.
- Does Super Resolution Fluorescence Microscopy Obsolete Previous Microscopic Approaches to Protein Co-localization?
- Recent advances using green and red fluorescent protein variants
- Fluorescent two‐photon nanolithography
- Centromeres in cell division, evolution, nuclear organization and disease
- Resolution scaling in STED microscopy.
- Fluorescence Interferometry
- Reduction of photobleaching and photodamage in single molecule detection: observing single actin monomer in skeletal myofibrils.
- Visualization and orchestration of the dynamic molecular society in cells
- Imaging Leishmania development in their host cells.
- A route to sub-diffraction-limited CARS Microscopy.
- Early T‐cell activation biophysics
- Dynamic SpoIIIE assembly mediates septal membrane fission during Bacillus subtilis sporulation.
- A photoactivatable marker protein for pulse-chase imaging with superresolution
- The use of aequorins to record and visualize Ca(2+) dynamics: from subcellular microdomains to whole organisms.
- Central dogma at the single-molecule level in living cells
- Synaptic plasticity in sleep: learning, homeostasis, and disease
- Beam position stabilization for a confocal multiphoton microscope.
- Deep Molecular Diversity of Mammalian Synapses: Why It Matters and How to Measure It
- Live‐Cell Super‐Resolution Imaging Goes Multicolor
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