A genetically-encoded fluorescent biosensor for visualization of acetyl-CoA in live cells, Smith et al, PancACe HeLa time lapse experiments, original images

Published: 23 December 2024| Version 1 | DOI: 10.17632/rjs429tkz9.1
Contributor:
Katharine Diehl

Description

These data are raw image files from fluorescence microscopy analysis of HeLa cells in the study "A genetically-encoded fluorescent biosensor for visualization of acetyl-CoA in live cells," Smith et al. The processed data derived from these images is provided in the manuscript and in the supplemental data files published with it. Likewise, detailed protocols for data collection and image analysis are provided in the manuscript and supplemental files. The Python script used for batch processing of images via Fiji is available at https://github.com/Adamcolligan/pancace (DOI: 10.5281/zenodo.14532573). These images are from the time lapse experiments described in Figure S10 and Data File S5 of the publication. The files are in the .tif format as they were directly exported from Leica Application Suite X. Important filename information: Well- Every filename has a designation for the well in the microplate that was imaged (e.g., B2, B3, B4, C2). The spreadsheet included herein and Data File S5 of the publication provide a key for which well contained which experimental condition. Note that some wells were not utilized in every experiment and that some wells contained experimental conditions that were not ultimately published and so were excluded from inclusion herein. Position- The position denotes the area within the well that was imaged ("Position1"). Typically, 10 positions were collected per well. Time- The order in which the image was taken is described by "tx" in the filename (e.g., t00, t01, t02). The microscope cycled through measuring all the positions/wells in the same order in an interval of 15 min total. Images without any "tx" in the filename were taken before the media change was performed to begin the time lapse experiment. Channel designation- There are two images for each Position within each Well. Channel 00 ("ch_00") denotes the image collected with excitation light of 405 nm. Channel 01 ("ch_01") denotes the image collected with excitation light of 488 nm. For both channel images, light of 515 nm was detected.

Files

Institutions

University of Utah

Categories

Microscopy, Biosensor, Confocal Microscopy, Fluorescence Microscopy, Optical Biosensor

Funding

National Institute of General Medical Sciences

R35GM143080

Licence