Advanced processing and analysis of conventional confocal microscopy generated scanning FCS data
نویسندگان
چکیده
Scanning Fluorescence Correlation Spectroscopy (scanning FCS) is a variant of conventional point FCS that allows molecular diffusion at multiple locations to be measured simultaneously. It enables disclosure of potential spatial heterogeneity in molecular diffusion dynamics and also the acquisition of a large amount of FCS data at the same time, providing large statistical accuracy. Here, we optimize the processing and analysis of these large-scale acquired sets of FCS data. On one hand we present FoCuS-scan, scanning FCS software that provides an end-to-end solution for processing and analysing scanning data acquired on commercial turnkey confocal systems. On the other hand, we provide a thorough characterisation of large-scale scanning FCS data over its intended time-scales and applications and propose a unique solution for the bias and variance observed when studying slowly diffusing species. Our manuscript enables researchers to straightforwardly utilise scanning FCS as a powerful technique for measuring diffusion across a broad range of physiologically relevant length scales without specialised hardware or expensive software.
منابع مشابه
Raster Image Correlation Spectroscopic Analysis of Intranuclear Molecular Dynamics
In contrast to conventional epi-illumination microscopy in confocal laser scanning microscopy images are acquired sequentially either in point scanning or line scanning mode. This scanning approach therefore contains spatio-temporal information, which can be used to obtain insight into molecular dynamics, e.g. diffusion coefficients of fluorescently labeled probes. Raster Image Correlation Spec...
متن کاملCharacterization of flow direction in microchannels and zebrafish blood vessels by scanning fluorescence correlation spectroscopy.
The investigation of flow profiles in microstructures and tissues by fluorescence correlation spectroscopy (FCS) has been a challenging topic in the past decade. Due to its inherent optical configuration, a circular focused laser beam, FCS is unable to resolve microfluidic flow directions. Earlier schemes reported the use of two laser beams or the use of nonsymmetrical laser foci to break the s...
متن کاملNon-scanning Fluorescence Confocal Microscopy using Laser Speckle Illumination
Confocal scanning microscopy (CSM) is a much used and advantageous form of microscopy. Although CSM is superior to conventional microscopy in many respects, a major disadvantage is the complexity of the scanning process and the sometimes long time to perform the scan. In this thesis a novel non-scanning fluorescence confocal microscopy is investigated. The method uses a random timevarying speck...
متن کاملO-21: Differential Expression and Epigenetic Pattern of HOX Family Genes in Cumulus Cells of Mature MII Oocytes from Patients with Polycystic Ovary Syndrome
Background Ovarian tissue cryopreservation represents a promising strategy to preserve the ovarian function in cancer patients. It is usually performed by slow freezing/rapid thawing (SF/RT). Recent studies emphasize an ultrarapid cryopreservation procedure, vitrification/warming (V/W), since it might prevent damages due to ice crystal formation. Comparative studies between the cryopreservation...
متن کاملChloroplast and Cell Imaging at Submicron Resolution by Two-Photon Excitation
Multi-photon (MPE) NIR excitation of fluorophores--attached as labels to biopolymers like proteins and nucleic acids, or bound at specific biomembrane sites-is one of the most attractive options in biological applications of laser scanning microscopy. Many of the serious problems encountered in spectroscopic measurements of living tissue, such as photodamage, light scattering and auto-fluoresce...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2017