000217161 001__ 217161
000217161 005__ 20190317000416.0
000217161 0247_ $$2doi$$a10.5075/epfl-thesis-6905
000217161 02470 $$2urn$$aurn:nbn:ch:bel-epfl-thesis6905-4
000217161 02471 $$2nebis$$a10605860
000217161 037__ $$aTHESIS 000217161 041__$$aeng
000217161 088__ $$a6905 000217161 245__$$aNanoscopy in nonlinear scanning fluorescence imaging systems
000217161 269__ $$a2016 000217161 260__$$aLausanne$$bEPFL$$c2016
000217161 300__ $$a133 000217161 336__$$aTheses
000217161 502__ $$aProf. Bart Deplancke (président) ; Prof. Demetri Psaltis (directeur de thèse) ; Prof. Aleksandra Radenovic, Prof. Rachel Grange, Dr Colin Sheppard (rapporteurs) 000217161 520__$$aIn the last 30 years, superresolution in optical microscopy has been a major field of research. During this time, different techniques have been created to break the diffraction limit in order to make observations at a nanometric scale. Given that optical microscopy is non-invasive, those superresolution methods pave the way for a better understanding of biological mechanism at a molecular level. Most of those methods are based on a nonlinear interaction between the excitation light intensity and the sample response (often fluorescent signal). In the same time, nanodiamonds containing fluorescent defects have been proven to be a choice probe for superresolution nanos-copy since they exhibit a strong and stable fluorescent signal even under high light intensities exposure (often required to obtain nonlinear photoresponse). Nanodiamonds containing Nitrogen Vacancy (NV) defects that exhibit a red fluorescent signal had been previously shown to be a viable biomarker for STED superresolved image. First, we demonstrated that green fluorescent nanodia-monds containing Nitrogen-Vacancy-Nitrogen (NVN) defects can be used with a Stimulated Emission Depletion (STED) superreso-lution microscope. Then, we implemented a STED microscope in our lab and compared the properties of NVN and NV centers for STED imaging. We conclude that even if nanodiamonds with NVN defects are less intense, they can be used as a second color nonbleaching biomarker. To illustrate the potential use of green nanodiamonds as bio-compatible probe, we superresolved them internalized into a cell with STED microscopy. Second, we tried to work on one of the main limitation in STED nanoscopy: the lack of information in the axial direction within a single scan. We combined our home made STED microscope with a Double Helix phase mask that modifies the detection point spread function in order to obtain axial localization of the superresolved emitters. We achieved three dimensional localization of nanometric fluorescent emitters but we note that photobleaching was the main limitation of this approach with organic dyes. We discussed different solutions to limit the photobleaching and their feasibility.  We also worked on a different superresolution technique that we named Computational Nonlinear Saturated (CNS) microscopy. We showed that with digital post treatment of the acquired data, a nonlinear photoresponse can be harnessed to any scanning microscope equipped with a camera detector to enhance the resolution. We demonstrated that increasing the excitation power and inducing fluorescence saturation, it is possible to break the diffraction limit in a conventional confocal microscope (after data post-treatment). However, with this method, we did not obtain a gain in resolution as high as with other superresolution tech-niques involving fluorescence saturation, such as saturated structured illumination microscopy. To understand the origin of this limitation, we carried out simulation to investigate the performance of CNS microscopy in noisy environments compared with wide field techniques. We propose alternative implementation and quantify the possible resolution gain with simulations. Finally, we demonstrated how a technique, initially created for optical microscopy, can be adapted to lensless endoscopic imaging...
000217161 6531_ $$aSuperresolution microscopy 000217161 6531_$$aDouble-helix localization
000217161 6531_ $$aEndoscopic imaging 000217161 700__$$0245216$$aLaporte, Grégoire Pierre Jean$$g201753
000217161 720_2 $$0244715$$aPsaltis, Demetri$$edir.$$g174684
000217161 8564_ $$s23597912$$uhttps://infoscience.epfl.ch/record/217161/files/EPFL_TH6905.pdf$$yn/a$$zn/a
000217161 909C0 $$0252333$$pLO$$xU11723 000217161 909CO$$ooai:infoscience.tind.io:217161$$pthesis$$pthesis-bn2018$$pDOI$$pSTI$$qDOI2$$qGLOBAL_SET
000217161 917Z8 $$x108898 000217161 917Z8$$x108898
000217161 918__ $$aSTI$$cIMT$$dEDBB 000217161 919__$$aLO
000217161 920__ $$a2016-3-11$$b2016
000217161 970__ $$a6905/THESES 000217161 973__$$aEPFL$$sPUBLISHED 000217161 980__$$aTHESIS