Publication | Closed Access
Practical Chemical Synthesis of Atypical Ubiquitin Chains by Using an Isopeptide‐Linked Ub Isomer
21
Citations
39
References
2017
Year
Diversity Oriented SynthesisAtypical UbiquitinBiochemistryProtein AssemblyAtypical Ubiquitin ChainsAccessible PremadeDiversity-oriented SynthesisNatural SciencesBioconjugationMolecular BiologyIsopeptide‐linked Ub IsomerPeptide SynthesisPractical Chemical SynthesisAnalytical UltracentrifugationChemical BiologyAbstract Chemical UbiquitinationMacromolecular AssembliesSmall Molecules
Abstract Chemical ubiquitination is an effective approach for accessing structurally defined, atypical ubiquitin (Ub) chains that are difficult to prepare by other techniques. Herein, we describe a strategy that uses a readily accessible premade isopeptide‐linked 76‐mer (isoUb), which has an N‐terminal Cys and a C‐terminal hydrazide, as the key building block to assemble atypical Ub chains in a modular fashion. This method avoids the use of auxiliary‐modified Lys and instead employs the canonical and therefore more robust Cys‐based native chemical ligation technique. The efficiency and capacity of this isoUb‐based strategy is exemplified by the cost‐effective synthesis of several linkage‐ and length‐defined atypical Ub chains, including K27‐linked tetra‐Ub and K11/K48‐branched tri‐, tetra‐, penta‐, and hexa‐Ubs.
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