Chemical Tools for Probing the Ub/Ubl Conjugation Cascades

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Abstract
Conjugation of ubiquitin (Ub) and structurally related ubiquitin‐like proteins (Ubls), essential for many cellular processes, employs multi‐step reactions orchestrated by specific E1, E2 and E3 enzymes. The E1 enzyme activates the Ub/Ubl C‐terminus in an ATP‐dependent process that results in the formation of a thioester linkage with the E1 active site cysteine. The thioester‐activated Ub/Ubl is transferred to the active site of an E2 enzyme which then interacts with an E3 enzyme to promote conjugation to the target substrate. The E1‐E2‐E3 enzymatic cascades utilize labile intermediates, extensive conformational changes, and vast combinatorial diversity of short‐lived protein‐protein complexes to conjugate Ub/Ubl to various substrates in a regulated manner. In this review, we discuss various chemical tools and methods used to study the consecutive steps of Ub/Ubl activation and conjugation, which are often too elusive for direct studies. We focus on methods developed to probe enzymatic activities and capture and characterize stable mimics of the transient intermediates and transition states, thereby providing insights into fundamental mechanisms in the Ub/Ubl conjugation pathways.
Funding Information
  • National Institutes of Health (R35GM118080)

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