Summary of ssbd-repos-000279

SSBD:database
URL

Name
ssbd-repos-000279 (279-Suzuki-CaspaseActivity)
URL
DOI
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Title
Live imaging of caspase cascades activity in apoptosis-induced HeLa cells.
Description
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Submited Date
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Release Date
2023-07-20
Updated Date
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License
Funding information
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File formats
Data size
5.6 GB

Organism
Homo sapiens
Strain
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Cell Line
HeLa cell
Genes
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Proteins
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GO Molecular Function (MF)
cysteine-type endopeptidase activity involved in apoptotic process, cysteine-type endopeptidase activity
GO Biological Process (BP)
execution phase of apoptosis
GO Cellular Component (CC)
caspase complex
Study Type
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Imaging Methods
fluorescence microscopy, confocal microscopy

Method Summary
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Related paper(s)

Miho Suzuki, Yutaka Shindo, Ryu Yamanaka, Kotaro Oka (2022) Live imaging of apoptotic signaling flow using tunable combinatorial FRET-based bioprobes for cell population analysis of caspase cascades., Scientific reports, Volume 12, Number 1, pp. 21160

Published in 2022 Dec 7 (Electronic publication in Dec. 7, 2022, midnight )

(Abstract) Understanding cellular signaling flow is required to comprehend living organisms. Various live cell imaging tools have been developed but challenges remain due to complex cross-talk between pathways and response heterogeneities among cells. We have focused on multiplex live cell imaging for statistical analysis to address the difficulties and developed simple multiple fluorescence imaging system to quantify cell signaling at single-cell resolution using Forster Resonance Energy Transfer (FRET)-based chimeric molecular sensors comprised of fluorescent proteins and dyes. The dye-fluorescent protein conjugate is robust for a wide selection of combinations, facilitating rearrangement for coordinating emission profile of molecular sensors to adjust for visualization conditions, target phenomena, and simultaneous use. As the molecular sensor could exhibit highly sensitive in detection for protease activity, we customized molecular sensor of caspase-9 and combine the established sensor for caspase-3 to validate the system by observation of caspase-9 and -3 dynamics simultaneously, key signaling flow of apoptosis. We found cumulative caspase-9 activity rather than reaction rate inversely regulated caspase-3 execution times for apoptotic cell death. Imaging-derived statistics were thus applied to discern the dominating aspects of apoptotic signaling unavailable by common live cell imaging and proteomics protein analysis. Adopted to various visualization targets, the technique can discriminate between rivalling explanations and should help unravel other protease involved signaling pathways.

Contact(s)
Miho Suzuki
Organization(s)
Graduate School of Science and Engineering, Saitama University , Department of Applied Chemistry
Image Data Contributors
Quantitative Data Contributors

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