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Profiling and verifying the substrates of E3 ubiquitin ligase Rsp5 in yeast cells

Yeast is an essential model organism for studying protein ubiquitination pathways; however, identifying the direct substrates of E3 in the cell presents a challenge. Here, we present a protocol for using the orthogonal ubiquitin transfer (OUT) cascade to profile the substrate specificity of yeast E3...

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Autores principales: Fang, Shuai, Chen, Geng, Wang, Yiyang, Ganti, Rakhee, Chernova, Tatiana A., Zhou, Li, Jacobs, Savannah E., Duong, Duc, Kiyokawa, Hiroaki, Chernoff, Yury O., Li, Ming, Shcherbik, Natalia, Zhao, Bo, Yin, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10440593/
https://www.ncbi.nlm.nih.gov/pubmed/37561636
http://dx.doi.org/10.1016/j.xpro.2023.102489
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author Fang, Shuai
Chen, Geng
Wang, Yiyang
Ganti, Rakhee
Chernova, Tatiana A.
Zhou, Li
Jacobs, Savannah E.
Duong, Duc
Kiyokawa, Hiroaki
Chernoff, Yury O.
Li, Ming
Shcherbik, Natalia
Zhao, Bo
Yin, Jun
author_facet Fang, Shuai
Chen, Geng
Wang, Yiyang
Ganti, Rakhee
Chernova, Tatiana A.
Zhou, Li
Jacobs, Savannah E.
Duong, Duc
Kiyokawa, Hiroaki
Chernoff, Yury O.
Li, Ming
Shcherbik, Natalia
Zhao, Bo
Yin, Jun
author_sort Fang, Shuai
collection PubMed
description Yeast is an essential model organism for studying protein ubiquitination pathways; however, identifying the direct substrates of E3 in the cell presents a challenge. Here, we present a protocol for using the orthogonal ubiquitin transfer (OUT) cascade to profile the substrate specificity of yeast E3 Rsp5. We describe steps for OUT profiling, proteomics analysis, in vitro and in cell ubiquitination, and stability assay. The protocol can be adapted for identifying and verifying the ubiquitination targets of other E3s in yeast. For complete details on the use and execution of this protocol, please refer to Wang et al.(1)
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spelling pubmed-104405932023-08-22 Profiling and verifying the substrates of E3 ubiquitin ligase Rsp5 in yeast cells Fang, Shuai Chen, Geng Wang, Yiyang Ganti, Rakhee Chernova, Tatiana A. Zhou, Li Jacobs, Savannah E. Duong, Duc Kiyokawa, Hiroaki Chernoff, Yury O. Li, Ming Shcherbik, Natalia Zhao, Bo Yin, Jun STAR Protoc Protocol Yeast is an essential model organism for studying protein ubiquitination pathways; however, identifying the direct substrates of E3 in the cell presents a challenge. Here, we present a protocol for using the orthogonal ubiquitin transfer (OUT) cascade to profile the substrate specificity of yeast E3 Rsp5. We describe steps for OUT profiling, proteomics analysis, in vitro and in cell ubiquitination, and stability assay. The protocol can be adapted for identifying and verifying the ubiquitination targets of other E3s in yeast. For complete details on the use and execution of this protocol, please refer to Wang et al.(1) Elsevier 2023-08-09 /pmc/articles/PMC10440593/ /pubmed/37561636 http://dx.doi.org/10.1016/j.xpro.2023.102489 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Fang, Shuai
Chen, Geng
Wang, Yiyang
Ganti, Rakhee
Chernova, Tatiana A.
Zhou, Li
Jacobs, Savannah E.
Duong, Duc
Kiyokawa, Hiroaki
Chernoff, Yury O.
Li, Ming
Shcherbik, Natalia
Zhao, Bo
Yin, Jun
Profiling and verifying the substrates of E3 ubiquitin ligase Rsp5 in yeast cells
title Profiling and verifying the substrates of E3 ubiquitin ligase Rsp5 in yeast cells
title_full Profiling and verifying the substrates of E3 ubiquitin ligase Rsp5 in yeast cells
title_fullStr Profiling and verifying the substrates of E3 ubiquitin ligase Rsp5 in yeast cells
title_full_unstemmed Profiling and verifying the substrates of E3 ubiquitin ligase Rsp5 in yeast cells
title_short Profiling and verifying the substrates of E3 ubiquitin ligase Rsp5 in yeast cells
title_sort profiling and verifying the substrates of e3 ubiquitin ligase rsp5 in yeast cells
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10440593/
https://www.ncbi.nlm.nih.gov/pubmed/37561636
http://dx.doi.org/10.1016/j.xpro.2023.102489
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