Protocol for detecting and quantifying hATF4-HA in non-stress versus stress conditions using automated and quantitative Jess western blotting
Language English Country United States Media print-electronic
Document type Journal Article
PubMed
39570747
PubMed Central
PMC11617455
DOI
10.1016/j.xpro.2024.103454
PII: S2666-1667(24)00619-1
Knihovny.cz E-resources
- Keywords
- cell culture, gene expression, protein expression and purification,
- MeSH
- Stress, Physiological * physiology MeSH
- HEK293 Cells MeSH
- Hemagglutinins genetics metabolism MeSH
- Humans MeSH
- Activating Transcription Factor 4 * metabolism genetics MeSH
- Blotting, Western * methods MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- ATF4 protein, human MeSH Browser
- Hemagglutinins MeSH
- Activating Transcription Factor 4 * MeSH
Activating transcription factor 4 (ATF4) is a key player in the integrated stress response, whose expression is subject to tight translational control. Studying its stress-provoked induction, accompanied by the general translational shutdown, is intricate because the expression of reference genes declines rapidly, and finding appropriate normalization controls is challenging. We present a protocol for human hemagglutinin-tagged ATF4 (hATF4-HA) detection and high-throughput quantification in non-stress versus stress conditions using automated and quantitative western blotting. We describe steps for seeding cells, transfecting plasmids, thapsigargin treatment, sample preparation, and target protein detection. For complete details on the use and execution of this protocol, please refer to Smirnova et al.1.
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Smirnova A.M., Hronová V., Mohammad M.P., Herrmannová A., Gunišová S., Petráčková D., Halada P., Coufal Š., Świrski M., Rendleman J., et al. Stem-loop-induced ribosome queuing in the uORF2/ATF4 overlap fine-tunes stress-induced human ATF4 translational control. Cell Rep. 2024;43 doi: 10.1016/j.celrep.2024.113976. PubMed DOI PMC
Herrmannová A., Prilepskaja T., Wagner S., Sikrova D., Zeman J., Poncova K., Valasek L.S. Adapted formaldehyde gradient cross-linking protocol implicates human eIF3d and eIF3c, k and l subunits in the 43S and 48S pre-initiation complex assembly, respectively. Nucleic Acids Res. 2020;48:1969–1984. doi: 10.1093/nar/gkz1185. PubMed DOI PMC
Pfaffl M.W. A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res. 2001;29 doi: 10.1093/nar/29.9.e45. PubMed DOI PMC