Shim et al., 2012 - Google Patents
Super-resolution fluorescence imaging of organelles in live cells with photoswitchable membrane probesShim et al., 2012
View HTML- Document ID
- 15340847726210577147
- Author
- Shim S
- Xia C
- Zhong G
- Babcock H
- Vaughan J
- Huang B
- Wang X
- Xu C
- Bi G
- Zhuang X
- Publication year
- Publication venue
- Proceedings of the National Academy of Sciences
External Links
Snippet
Imaging membranes in live cells with nanometer-scale resolution promises to reveal ultrastructural dynamics of organelles that are essential for cellular functions. In this work, we identified photoswitchable membrane probes and obtained super-resolution fluorescence …
- 210000004027 cells 0 title abstract description 60
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using infra-red, visible or ultra-violet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/64—Fluorescence; Phosphorescence
- G01N21/645—Specially adapted constructive features of fluorimeters
- G01N21/6456—Spatial resolved fluorescence measurements; Imaging
- G01N21/6458—Fluorescence microscopy
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using infra-red, visible or ultra-violet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/64—Fluorescence; Phosphorescence
- G01N21/6428—Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes"
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
- G01N33/5008—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using infra-red, visible or ultra-violet light
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/65—Raman scattering
- G01N2021/653—Coherent methods [CARS]
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS, OR APPARATUS
- G02B21/00—Microscopes
- G02B21/16—Microscopes adapted for ultra-violet illumination; Fluorescence microscopes
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Shim et al. | Super-resolution fluorescence imaging of organelles in live cells with photoswitchable membrane probes | |
Burnette et al. | Bleaching/blinking assisted localization microscopy for superresolution imaging using standard fluorescent molecules | |
Wang et al. | A photostable fluorescent marker for the superresolution live imaging of the dynamic structure of the mitochondrial cristae | |
Liu et al. | Multi-color live-cell STED nanoscopy of mitochondria with a gentle inner membrane stain | |
Tuijtel et al. | Correlative cryo super-resolution light and electron microscopy on mammalian cells using fluorescent proteins | |
Beghin et al. | Localization-based super-resolution imaging meets high-content screening | |
Manley et al. | High-density mapping of single-molecule trajectories with photoactivated localization microscopy | |
Nägerl et al. | Live-cell imaging of dendritic spines by STED microscopy | |
Shroff et al. | Live-cell photoactivated localization microscopy of nanoscale adhesion dynamics | |
Robin et al. | Single-molecule analysis of cell surface dynamics in Caenorhabditis elegans embryos | |
Godin et al. | Super-resolution microscopy approaches for live cell imaging | |
Lidke et al. | Advances in high-resolution imaging–techniques for three-dimensional imaging of cellular structures | |
Rego et al. | Nonlinear structured-illumination microscopy with a photoswitchable protein reveals cellular structures at 50-nm resolution | |
Göttfert et al. | Strong signal increase in STED fluorescence microscopy by imaging regions of subdiffraction extent | |
Sauer | Localization microscopy coming of age: from concepts to biological impact | |
Zhuang | Nano-imaging with STORM | |
Lew et al. | Three-dimensional superresolution colocalization of intracellular protein superstructures and the cell surface in live Caulobacter crescentus | |
Sengupta et al. | Superresolution imaging of biological systems using photoactivated localization microscopy | |
Keller | Imaging morphogenesis: technological advances and biological insights | |
Dedecker et al. | Widely accessible method for superresolution fluorescence imaging of living systems | |
Coltharp et al. | Superresolution microscopy for microbiology | |
Kiuchi et al. | Multitarget super-resolution microscopy with high-density labeling by exchangeable probes | |
Ries et al. | Modular scanning FCS quantifies receptor-ligand interactions in living multicellular organisms | |
Biteen et al. | Three‐dimensional super‐resolution imaging of the midplane protein FtsZ in live Caulobacter crescentus cells using astigmatism | |
Hedde et al. | Online image analysis software for photoactivation localization microscopy |