Jakobs et al., 2020 - Google Patents
Light microscopy of mitochondria at the nanoscaleJakobs et al., 2020
View PDF- Document ID
- 15042233639028446757
- Author
- Jakobs S
- Stephan T
- Ilgen P
- Brüser C
- Publication year
- Publication venue
- Annual review of biophysics
External Links
Snippet
Mitochondria are essential for eukaryotic life. These double-membrane organelles often form highly dynamic tubular networks interacting with many cellular structures. Their highly convoluted contiguous inner membrane compartmentalizes the organelle, which is crucial …
- 210000003470 Mitochondria 0 title abstract description 100
Classifications
-
- 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
- G01N33/502—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 for testing non-proliferative effects
-
- 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
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS, OR APPARATUS
- G02B21/00—Microscopes
- G02B21/0004—Microscopes specially adapted for specific applications
- G02B21/002—Scanning microscopes
- G02B21/0024—Confocal scanning microscopes (CSOMs) or confocal "macroscopes"; Accessories which are not restricted to use with CSOMs, e.g. sample holders
- G02B21/0052—Optical details of the image generation
- G02B21/0076—Optical details of the image generation arrangements using fluorescence or luminescence
-
- 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 |
|---|---|---|
| Jakobs et al. | Light microscopy of mitochondria at the nanoscale | |
| Sahl et al. | Fluorescence nanoscopy in cell biology | |
| Möckl et al. | Super-resolution microscopy with single molecules in biology and beyond–essentials, current trends, and future challenges | |
| Spahn et al. | Whole-cell, 3D, and multicolor STED imaging with exchangeable fluorophores | |
| Liu et al. | Multi-color live-cell STED nanoscopy of mitochondria with a gentle inner membrane stain | |
| Lavis | Chemistry is dead. Long live chemistry! | |
| Huang et al. | Super-resolution fluorescence microscopy | |
| Lidke et al. | Advances in high-resolution imaging–techniques for three-dimensional imaging of cellular structures | |
| Godin et al. | Super-resolution microscopy approaches for live cell imaging | |
| van de Linde et al. | Live-cell super-resolution imaging with synthetic fluorophores | |
| Hell et al. | The 2015 super-resolution microscopy roadmap | |
| Müller et al. | STED microscopy and its applications: new insights into cellular processes on the nanoscale | |
| Huang et al. | Molecular-level investigation of the structure, transformation, and bioactivity of single living fission yeast cells by time-and space-resolved Raman spectroscopy | |
| Kahya et al. | Fluorescence correlation studies of lipid domains in model membranes | |
| Joo et al. | Advances in single-molecule fluorescence methods for molecular biology | |
| Sezgin et al. | Elucidating membrane structure and protein behavior using giant plasma membrane vesicles | |
| Tyson et al. | Extremely bright, near-IR emitting spontaneously blinking fluorophores enable ratiometric multicolor nanoscopy in live cells | |
| Begemann et al. | Correlative light electron microscopy: connecting synaptic structure and function | |
| Sánchez et al. | Lipid− protein interactions revealed by two-photon microscopy and fluorescence correlation spectroscopy | |
| Auer et al. | Nanometer‐scale multiplexed super‐resolution imaging with an economic 3D‐DNA‐PAINT microscope | |
| Herbert et al. | Single-molecule localization super-resolution microscopy: deeper and faster | |
| Thompson et al. | HIDE probes: A new toolkit for visualizing organelle dynamics, longer and at super-resolution | |
| Lo et al. | Novel super-resolution capable mitochondrial probe, MitoRed AIE, enables assessment of real-time molecular mitochondrial dynamics | |
| De Keersmaecker et al. | Mapping transient protein interactions at the nanoscale in living mammalian cells | |
| Yang et al. | Green fluorescent probe for imaging His6-tagged proteins inside living cells |