ABSTRACT
In this work we present how to entirely remove the scattering ambiguity present in existing multiphoton multifocal systems. This is achieved through the development and implementation of single-element detection systems that incorporate high-speed photon-counting electronics. These systems can be used to image entire volumes in the time it takes to perform a single transverse scan (four depths simultaneously at a rate of 30 Hz). In addition, this capability is further exploited to accomplish single-element detection of multiple modalities (two photon excited fluorescence and second harmonic generation) and to perform efficient image deconvolution. Finally, we demonstrate a new system that promises to significantly simplify this promising technology.
Subject(s)
Microscopy, Fluorescence, Multiphoton/methods , Molecular Imaging/methods , Scattering, Radiation , Animals , Cellulose/metabolism , Drosophila melanogaster/cytology , Image Processing, Computer-Assisted , Luminescent Proteins/metabolism , Starch/chemistry , Zea mays/chemistry , Red Fluorescent ProteinABSTRACT
Multifocal multiphoton microscopy (MMM) in the biological and medical sciences has become an important tool for obtaining high resolution images at video rates. While current implementations of MMM achieve very high frame rates, they are limited in their applicability to essentially those biological samples that exhibit little or no scattering. In this paper, we report on a method for MMM in which imaging detection is not necessary (single element point detection is implemented), and is therefore fully compatible for use in imaging through scattering media. Further, we demonstrate that this method leads to a new type of MMM wherein it is possible to simultaneously obtain multiple images and view differences in excitation parameters in a single shot.
ABSTRACT
We present a prism-based spectrometer integrated into a multifocal, multiphoton microscope. The multifocal configuration facilitates interrogation of samples under different excitation conditions. Notably, the image plane of the microscope and the image plane of the spectrometer are coincident eliminating the need for an intermediate image plane containing an entrance slit. An EM-CCD detector provides sufficient gain for spectral interrogation of single-emitters. We employ this spectrometer to observe spectral shifts in the two-photon excitation fluorescence emission of single CdSe nanodots as a function of excitation polarization.
Subject(s)
Microscopy, Fluorescence, Multiphoton/instrumentation , Spectrophotometry/instrumentation , Cadmium Compounds/chemistry , Cadmium Compounds/radiation effects , Optical Devices , Quantum Dots , Selenium Compounds/chemistry , Selenium Compounds/radiation effectsABSTRACT
A challenge for nonlinear imaging in living tissue is to maximize the total fluorescent yield from each fluorophore. We investigated the emission rates of three fluorophores-rhodamine B, a red fluorescent protein, and CdSe quantum dots-while manipulating the phase of the laser excitation pulse at the focus. In all cases a transform-limited pulse maximized the total yield to insure the highest signal-to-noise ratio. Further, we find evidence of fluorescence antibleaching in quantum dot samples.
Subject(s)
Luminescent Proteins/chemistry , Microscopy, Confocal/methods , Microscopy, Fluorescence/methods , Quantum Dots , Rhodamines/chemistry , Biology/instrumentation , Cadmium Compounds/chemistry , Models, Theoretical , Photobleaching , Plant Cells , Selenium Compounds/chemistry , Red Fluorescent ProteinABSTRACT
We present the application of remote focusing to multiphoton laser scanning microscopy and utilize this technology to demonstrate simultaneous, programmable multi-layer imaging. Remote focusing is used to independently control the axial location of multiple focal planes that can be simultaneously imaged with single element detection. This facilitates volumetric multiphoton imaging in scattering specimens and can be practically scaled to a large number of focal planes. Further, it is demonstrated that the remote focusing control can be synchronized with the lateral scan directions, enabling imaging in orthogonal scan planes.
