Lighting up the cell surface with evanescent wave microscopy

Trends in Cell Biology

Volumn 11, Issue 7, 2001, Pages 298-303

  Toomre, Derek ^a,b   Manstein, Dietmar J ^a  

^a MAX PLANCK INSTITUTE FOR MEDICAL RESEARCH   (Germany)

^b YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GREEN FLUORESCENT PROTEIN;

CELL MEMBRANE; CELL SURFACE; EXOCYTOSIS; FLUORESCENCE MICROSCOPY; MEMBRANE FUSION; PRIORITY JOURNAL; REVIEW; SIGNAL TRANSDUCTION; SYNAPSE VESICLE;

EID: 0035399557     PISSN: 09628924     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0962-8924(01)02027-X     Document Type: Review

References (29)

1. Total internal reflection fluorescence
2. Imaging transmitter release. II. A practical guide to evanescent-wave imaging
3. Single-molecule fluorescence detection of green fluorescence protein and application to single-protein dynamics
4. Single molecule detection in life science
5. Total internal reflection fluorescence: Applications in cellular biophysics
6. Application of total internal reflection fluorescence microscopy to study cell adhesion to biomaterials
7. A real-time view of life within 100 nm of the plasma membrane
8. Tracking single secretory granules in live chromaffin cells by evanescent-field fluorescence microscopy
9. Development of an objective lens with a high numerical aperture for light microscopy
10. Imaging constitutive exocytosis with total internal reflection fluorescence microscopy
11. Transport, capture and exocytosis of single synaptic vesicles at active zones
12. 2+ microdomains: New tools for understanding their roles in neurotransmitter release
13. Transport, docking and exocytosis of single secretory granules in live chromaffin cells
14. Tracking chromaffin granules on their way through the actin cortex
15. 2+-triggered peptide secretion in single cells imaged with green fluorescent protein and evanescent-wave microscopy
16. The last few milliseconds in the life of a secretory granule. Docking, dynamics and fusion visualized by total internal reflection fluorescence microscopy (TIRFM)
17. Multiple stimulation-dependent processes regulate the size of the releasable pool of vesicles
18. Neuropeptide release by efficient recruitment of diffusing cytoplasmic secretory vesicles
19. Observing secretory granules with a multiangle evanescent wave microscope
20. Simultaneous evanescent wave imaging of insulin vesicle membrane and cargo during a single exocytotic event
21. Fusion of constitutive membrane traffic with the cell surface observed by evanescent wave microscopy
22. Multicolour imaging of post-Golgi sorting and trafficking in live cells
23. Imaging of single fluorescent molecules and individual ATP turnovers by single myosin molecules in aqueous solution
24. Direct observation of single kinesin molecules moving along microtubules
25. Comparative single-molecule and ensemble myosin enzymology: Sulfoindocyanine ATP and ADP derivatives
26. Single-molecule imaging of EGFR signalling on the surface of living cells
27. Endocytic vesicles move at the tips of actin tails in cultured mast cells
28. Lipid rafts and signal transduction
29. Spatial sensing in fibroblasts mediated by 3′ phosphoinositides