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Cytosolic Delivery of Functional Ubiquitin

Author(s)
Giancola, JoLynn B; Okon, Aniekan; Li, Yanfeng; Strieter, Eric R; Raines, Ronald T
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Abstract
The proteostasis network involves complex protein signaling cascades. The tagging of proteins with ubiquitin is central to thedegradation of cellular proteins, but understanding its exact role in processing proteins is complicated by the complexity andextent of its utilization within cells. Here, we describe the application of a traceless protein delivery strategy to effect the uptakeof exogenous ubiquitin into the cytosol of human cells. We find that coadministration of the endosomolytic peptides L17E and,especially, L17ER 4 provides not only cytosolic access to ubiquitin but also its functional incorporation into endogenous proteins.By enabling the study of semisynthetic ubiquitin variants in the human cytosol, this strategy could advance the field of ubiquitinbiology.
Date issued
2025-05-08
URI
https://hdl.handle.net/1721.1/162870
Department
Massachusetts Institute of Technology. Department of Chemistry
Journal
Journal of Peptide Science
Publisher
Wiley
Citation
Giancola, J., Okon, A., Li, Y., Strieter, E. and Raines, R. (2025), Cytosolic Delivery of Functional Ubiquitin. J Pept Sci, 31: e70026.
Version: Final published version

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