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A modular toolbox to generate complex polymeric ubiquitin architectures using orthogonal sortase enzymes
被引:0
|作者:
Maximilian Fottner
Maria Weyh
Stefan Gaussmann
Dominic Schwarz
Michael Sattler
Kathrin Lang
机构:
[1] Lab for Synthetic Biochemistry,Department of Chemistry
[2] Technical University of Munich,undefined
[3] Institute for Advanced Study,undefined
[4] TUM-IAS,undefined
[5] Laboratory of Organic Chemistry,undefined
[6] Department of Chemistry and Applied Biosciences,undefined
[7] ETH Zürich,undefined
[8] Bavarian NMR Center,undefined
[9] Department of Chemistry,undefined
[10] Technical University of Munich,undefined
[11] Institute of Structural Biology,undefined
[12] Helmholtz Zentrum München,undefined
来源:
Nature Communications
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/
12卷
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摘要:
The post-translational modification of proteins with ubiquitin (Ub) and Ub-like modifiers (Ubls) represents one of the most important regulators in eukaryotic biology. Polymeric Ub/Ubl chains of distinct topologies control the activity, stability, interaction and localization of almost all cellular proteins and elicit a variety of biological outputs. Our ability to characterize the roles of distinct Ub/Ubl topologies and to identify enzymes and receptors that create, recognize and remove these modifications is however hampered by the difficulty to prepare them. Here we introduce a modular toolbox (Ubl-tools) that allows the stepwise assembly of Ub/Ubl chains in a flexible and user-defined manner facilitated by orthogonal sortase enzymes. We demonstrate the universality and applicability of Ubl-tools by generating distinctly linked Ub/Ubl hybrid chains, and investigate their role in DNA damage repair. Importantly, Ubl-tools guarantees straightforward access to target proteins, site-specifically modified with distinct homo- and heterotypic (including branched) Ub chains, providing a powerful approach for studying the functional impact of these complex modifications on cellular processes.
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