Two-photon 3-D FIONA of individual quantum dots
Microscopy is performed by imaging individual quantum dots (QD) using two-photon (2P) microscopy of in an aqueous environment with widefield and point-scan excitations at nanometer accuracy.
1. A method of microscopy comprising the step of imaging individual quantum dots (QD) using two-photon (2P) microscopy in an aqueous environment with widefield and point-scan excitations at nanometer accuracy.
2. The method of claim 1 further comprising the step of using a thiol-containing reductant to suppress QD blinking.
3. The method of claim 1 further comprising the step of localizing the QDs with an accuracy of 2˜3 nm in all three dimensions by using a 9×9 matrix excitation hologram and an array detector
4. The method of claim 1 further comprising the step of using a holographic matrix in excitation and an electron multiplying charge coupled device (EMCCD) in detection.
5. The method of claim 1 wherein the imaging is performed at ambient (room) or cell-viability permissive temperature.
6. The method of claim 1 wherein the quantum dots are attached to a biological molecule, wherein the method images the molecule, wherein the molecule is present on or in a cell.
7. The method of claim 1 further comprising the steps of:
using a thiol-containing reductant to suppress QD blinking;
localizing the QDs with an accuracy of 2˜3 nm in all three dimensions by using a 9×9 matrix excitation hologram and an array detector; and
using a holographic matrix in excitation and an electron multiplying charge coupled device (EMCCD) in detection.
8. The method of claim 7 wherein the imaging is performed at ambient (room) or cell-viability permissive temperature.
9. The method of claim 7 wherein the quantum dots are attached to a biological molecule, wherein the method images the molecule, wherein the molecule is present on or in a cell.
10. An imaging system specifically adapted for implementing the method of claim 1 of imaging individual quantum dots (QD) using two-photon (2P) microscopy in an aqueous environment with wide-field and point-scan excitations at nanometer accuracy and comprising the components and arrangements as follows: a sample chamber, objective, a piezo stage, a CCD camera or photomultiplier tube (PMT), an IR laser, mirrors and lenses, configured so that light from the laser is directed by mirrors and focused by a lens into the back aperture of the objective and collimated through it to the sample chamber, mirrors and the piezo stage are under the objective scan the laser in x-y and z-axes, and images are transmitted to and recorded with the CCD camera or PMT.