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dc.contributor.authorMuir, Tom W.-
dc.date.accessioned2023-09-20T02:16:11Z-
dc.date.available2023-09-20T02:16:11Z-
dc.date.issued2023-
dc.identifier.otherOER000002339vi
dc.identifier.urihttp://dlib.hust.edu.vn/handle/HUST/23181-
dc.description.abstractThe post-translational regulation of protein function is involved in most cellular processes. As such, synthetic biology tools that operate at this level provide opportunities for manipulating cellular states. Here, we deploy a proximity-triggered protein trans-splicing technology to enable the time-resolved synthesis of target proteins from pre-made parts. The modularity of the strategy allows for the addition or removal of various control elements as a function of the splicing reaction, 20 in the process permitting the cellular location and/or activity state of starting materials and products to be differentiated. The approach is applied to a diverse set of proteins, including the kinase oncofusions BCR/ABL and DNAJB1/PRKACA where dynamic cellular phosphorylation events are dissected, revealing distinct phases of signaling and identifying molecular players connecting the oncofusion to cancer transformation as novel therapeutic targets of cancer cells.vi
dc.description.urihttps://www.biorxiv.org/content/10.1101/2023.07.10.548208v1.full.pdf+htmlvi
dc.formatPDFvi
dc.language.isoenvi
dc.publisherbioRxivvi
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Vietnam*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/vn/*
dc.subjectproteinvi
dc.subjecttín hiệu tế bàovi
dc.subjectquá trình tổng hợpvi
dc.subjectphân giảivi
dc.subject.lccTP248vi
dc.titleDistinct phases of cellular signaling revealed by time-resolved protein synthesisvi
dc.typeJournal Articlevi
dc.description.noteCC BY-NC-ND 4.0vi
Appears in Collections:OER - Kỹ thuật hóa học; Công nghệ sinh học - Thực phẩm; Công nghệ môi trường

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