SPIFEE -- A pipeline for analyzing traces of live-cell fluorescence microscopy data
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To properly respond to their environment, cells adjust the activity of key regulatory proteins and rates of gene expression. Methods to detect and quantify these forms of regulatory dynamics in living cells are of central importance for understanding cellular signaling events in both physiological and pathological conditions. Current technologies in this field make use of fluorescent probes to track cell signaling dynamics. Although these technologies have been used for decades, challenges remain. In particular, the segmentation, tracking, and interpretation of single cell dynamic data are time-consuming, prone to subjective errors, and often lacking in standardization across experiments. Here, we present SPIFEE, a data pipeline that uses experiment-dependent parameters to smooth noise and quantify key features of fluorescence data from time-lapse imaging studies. Processing data in this manner enhances and accelerates quantification of live-cell gene and protein expression, simplifies data analysis, and facilitates hypothesis generation.
Author Summary
Cells adjust protein activity and gene expression levels over time to respond to changes in their environment, a process referred to as cell signaling dynamics. Quantifying cell signaling dynamics in living cells often uses fluorescent probes, such as green fluorescent protein (GFP) and its spectral variants, to track changes in gene expression or protein activity over time. Challenges inherent in analyzing fluorescence data from single cells stem from biological and experimental noise, time-consuming quantification, and subjective errors. To address these challenges, we developed a computational tool called Signal Processing and Integrated Feature Extraction (SPIFEE). The pipeline improves the quality of fluorescence data analysis by reducing noise and extracting signal features in a way that is both intuitive and objective. The pipeline provides more accurate, rapid, and unbiased quantification of time-lapse microscopy data.
