Prof. Enrico Gratton, Founder and Principle Investigator
Laboratory of Fluorescence Dynamics, University of California, Irvine
The lab of Prof. Enrico Gratton at the University of California, Irvine, is interested in the dynamics of the cell interior. The group investigates this using microscopy combined with mathematical approaches such as ﬂuorescence correlation spectroscopy. As the founder and Principle Investigator of the Laboratory of Fluorescence Dynamics, Prof. Gratton’s team has developed numerous ﬂuorescence-based methods to measure diverse cell properties. This includes measurement of the absolute concentrations of molecules within cellular compartments, detection of aggregation of proteins and the detection of barriers to diffusion. Prof. Gratton also developed Globals for Images, a set of software packages to perform this analysis.
To reliably detect the incredibly small ﬂuctuations in image signal required for ﬂuorescence correlation spectroscopy – on the order of 10 electrons of signal – stable and predictable noise characteristics are necessary. Noise is an inherent feature of camera sensors and is corrected to reveal ﬂuorescent ﬂuctuations which are detected and measured. Typical experiments using EMCCD cameras require the noise characteristics, including correlated noise and light-independent pixel variance, to be mapped before every experiment to account for instability in the camera noise over time. After fast, time series ﬂuorescence imaging, the previously mapped noise is removed to detect the variance due to ﬂuorescent ﬂuctuations in each pixel, and allowed mathematical analysis of the signal. With ﬂuctuations in signal being less than 10 electrons in amplitude, high camera sensitivity and being able to accurately correct for the noise are crucial in providing the necessary signal to noise for this analysis.
Prof. Gratton now uses the Prime 95B back illuminated Scientific CMOS camera to take advantage of the stable noise and uncorrelated pixel noise properties.