TY - JOUR
T1 - Single-fluorophore imaging with an unmodified epifluorescence microscope and conventional video camera
AU - Adachi, K.
AU - Kinosita, K.
AU - Ando, T.
PY - 1999
Y1 - 1999
N2 - Single fluorophores in aqueous solution were imaged in real time with a conventional silicon-intensified target video camera connected to an unmodified commercial microscope (IX70, Olympus) with epifluorescence excitation with a high-pressure mercury lamp. Neither a powerful laser nor an extremely sensitive video camera was required. Three experimental systems were used to demonstrate quantitatively that individual, moving or stationary Cy3 fluorophores could be imaged with the microscope: Cy3-gelsolin attached to an actin filament sliding over heavy meromyosin, sliding actin filaments sparsely labelled with Cy3, and heavy meromyosin labelled with one or two Cy3 fluorophores. The results should encourage many laboratories to attempt 'single-molecule physiology' in which the functions and mechanisms of molecular machines are studied at the single-molecule level in an environment where the biological machines are fully active.
AB - Single fluorophores in aqueous solution were imaged in real time with a conventional silicon-intensified target video camera connected to an unmodified commercial microscope (IX70, Olympus) with epifluorescence excitation with a high-pressure mercury lamp. Neither a powerful laser nor an extremely sensitive video camera was required. Three experimental systems were used to demonstrate quantitatively that individual, moving or stationary Cy3 fluorophores could be imaged with the microscope: Cy3-gelsolin attached to an actin filament sliding over heavy meromyosin, sliding actin filaments sparsely labelled with Cy3, and heavy meromyosin labelled with one or two Cy3 fluorophores. The results should encourage many laboratories to attempt 'single-molecule physiology' in which the functions and mechanisms of molecular machines are studied at the single-molecule level in an environment where the biological machines are fully active.
KW - Cy3
KW - Epifluorescence microscope
KW - Single-molecule imaging
KW - SIT camera
UR - http://www.scopus.com/inward/record.url?scp=0032811041&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0032811041&partnerID=8YFLogxK
U2 - 10.1046/j.1365-2818.1999.00482.x
DO - 10.1046/j.1365-2818.1999.00482.x
M3 - Article
AN - SCOPUS:0032811041
SN - 0022-2720
VL - 195
SP - 125
EP - 132
JO - Journal of Microscopy
JF - Journal of Microscopy
IS - 2
ER -