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doi:10.22028/D291-38421
Titel: | Mapping the Degradable Kinome Provides a Resource for Expedited Degrader Development |
VerfasserIn: | Donovan, Katherine A. Ferguson, Fleur M. Bushman, Jonathan W. Eleuteri, Nicholas A. Bhunia, Debabrata Ryu, SeongShick Tan, Li Shi, Kun Yue, Hong Liu, Xiaoxi Dobrovolsky, Dennis Jiang, Baishan Wang, Jinhua Hao, Mingfeng You, Inchul Teng, Mingxing Liang, Yanke Hatcher, John Li, Zhengnian Manz, Theresa D. Groendyke, Brian Hu, Wanyi Nam, Yunju Sengupta, Sandip Cho, Hanna Shin, Injae Agius, Michael P. Ghobrial, Irene M. Ma, Michelle W. Che, Jianwei Buhrlage, Sara J. Sim, Taebo Gray, Nathanael S. Fischer, Eric S. |
Sprache: | Englisch |
Titel: | Cell |
Bandnummer: | 183 |
Heft: | 6 |
Seiten: | 1714–1731 |
Verlag/Plattform: | Elsevier |
Erscheinungsjahr: | 2020 |
Freie Schlagwörter: | ubiquitin PROTAC IMiD kinase degrader ubiquitin proteasome system targeted degradation E3 ligase |
DDC-Sachgruppe: | 500 Naturwissenschaften |
Dokumenttyp: | Journalartikel / Zeitschriftenartikel |
Abstract: | Targeted protein degradation (TPD) refers to the use of small molecules to induce ubiquitin-dependent degradation of proteins. TPD is of interest in drug development, as it can address previously inaccessible targets. However, degrader discovery and optimization remains an inefficient process due to a lack of understanding of the relative importance of the key molecular events required to induce target degradation. Here, we use chemo-proteomics to annotate the degradable kinome. Our expansive dataset provides chemical leads for 200 kinases and demonstrates that the current practice of starting from the highest potency binder is an ineffective method for discovering active compounds. We develop multitargeted degraders to answer fundamental questions about the ubiquitin proteasome system, uncovering that kinase degradation is p97 dependent. This work will not only fuel kinase degrader discovery, but also provides a blueprint for evaluating targeted degradation across entire gene families to accelerate understanding of TPD beyond the kinome. |
DOI der Erstveröffentlichung: | 10.1016/j.cell.2020.10.038 |
URL der Erstveröffentlichung: | http://dx.doi.org/10.1016/j.cell.2020.10.038 |
Link zu diesem Datensatz: | urn:nbn:de:bsz:291--ds-384218 hdl:20.500.11880/34670 http://dx.doi.org/10.22028/D291-38421 |
ISSN: | 0092-8674 |
Datum des Eintrags: | 7-Dez-2022 |
Bezeichnung des in Beziehung stehenden Objekts: | Supplemental Information |
In Beziehung stehendes Objekt: | https://ars.els-cdn.com/content/image/1-s2.0-S0092867420314458-mmc1.pdf https://ars.els-cdn.com/content/image/1-s2.0-S0092867420314458-mmc2.pdf https://ars.els-cdn.com/content/image/1-s2.0-S0092867420314458-mmc3.xlsx https://ars.els-cdn.com/content/image/1-s2.0-S0092867420314458-mmc4.xlsx https://ars.els-cdn.com/content/image/1-s2.0-S0092867420314458-mmc5.xlsx https://ars.els-cdn.com/content/image/1-s2.0-S0092867420314458-mmc6.xlsx https://ars.els-cdn.com/content/image/1-s2.0-S0092867420314458-mmc7.xlsx https://ars.els-cdn.com/content/image/1-s2.0-S0092867420314458-mmc8.xlsx https://ars.els-cdn.com/content/image/1-s2.0-S0092867420314458-mmc9.xlsx https://ars.els-cdn.com/content/image/1-s2.0-S0092867420314458-mmc10.xlsx https://ars.els-cdn.com/content/image/1-s2.0-S0092867420314458-mmc11.xlsx https://ars.els-cdn.com/content/image/1-s2.0-S0092867420314458-mmc12.xlsx |
Fakultät: | NT - Naturwissenschaftlich- Technische Fakultät |
Fachrichtung: | NT - Pharmazie |
Professur: | NT - Prof. Dr. Christian Ducho |
Sammlung: | SciDok - Der Wissenschaftsserver der Universität des Saarlandes |
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