A reporter of UV intensity delivered to the cytosol during photolytic uncaging.
نویسندگان
چکیده
Photolytic uncaging of biologically-active molecules within cells is a powerful technique. However, the delivery of uncaging light into the cytosol can vary between cell types, individual cells of the same type, and different loci within an individual cell because of optical differences in absorbance and light-scattering properties of the cytoplasm. Here, we demonstrate a simple technique for monitoring the magnitude of cytosolic ultraviolet delivery during uncaging, which also leaves a quantitative and persistent record of this within the cells. The simple method shown here provides a much needed universal monitor of the delivery of ultraviolet light to molecules within the cytosol, providing a much needed parameter for the correct interpretation of uncaging experiments.
منابع مشابه
In vitro and in vivo uncaging and bioluminescence imaging by using photocaged upconversion nanoparticles.
High temporal and spatial regulation of cellular activities, biological pathways, and gene expression is critical in complex biological processes. One remarkable technique that enables such control is the use of light to manipulate compounds that are photoactive (or photocaged) in various biological systems. Previously, this strategy has been used to map cellular functions, monitor the expressi...
متن کاملHigh efficient degradation of Cefixime using UV/TiO2 photocatalytic process: A comparison between photocatalytic and photolytic
Introduction: The existence of pharmaceuticals in aquatic ecosystem, their persistence and possible effects on living organisms and inefficient systems in removal of these compounds from water and wastewater are a growing concern. In this research, the UV/TiO2 photocatalytic degradation of Cefixime was investigated so as to identify if this method was efficient for removal of Cefixime or not. ...
متن کاملTwo-photon uncaging with fluorescence reporting: evaluation of the o-hydroxycinnamic platform.
This paper evaluates the o-hydroxycinnamic platform for designing efficient caging groups with fluorescence reporting upon one- and two-photon excitation. The model cinnamates are easily prepared in one step by coupling commercial or readily available synthons. They exhibit a large one-photon absorption that can be tuned in the near-UV range. Uncaging after one-photon excitation was investigate...
متن کاملMulti-photon Intracellular Sodium Imaging Combined with UV-mediated Focal Uncaging of Glutamate in CA1 Pyramidal Neurons
Multi-photon fluorescence microscopy has enabled the analysis of morphological and physiological parameters of brain cells in the intact tissue with high spatial and temporal resolution. Combined with electrophysiology, it is widely used to study activity-related calcium signals in small subcellular compartments such as dendrites and dendritic spines. In addition to calcium transients, synaptic...
متن کاملSource of nuclear calcium signals.
Transient increases of Ca2+ concentration in the nucleus regulate gene expression and other nuclear processes. We investigated whether nuclear Ca2+ signals could be regulated independently of the cytoplasm or were controlled by cytoplasmic Ca2+ signals. A fluorescent Ca2+ indicator that is targeted to the nucleus was synthesized by coupling a nuclear localization peptide to Calcium Green dextra...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Biophysical journal
دوره 98 7 شماره
صفحات -
تاریخ انتشار 2010