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Fidelity of Cotranslational Protein Targeting to the Endoplasmic Reticulum

Fidelity of protein targeting is essential for the proper biogenesis and functioning of organelles. Unlike replication, transcription and translation processes, in which multiple mechanisms to recognize and reject noncognate substrates are established in energetic and molecular detail, the mechanism...

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Autores principales: Hsieh, Hao-Hsuan, Shan, Shu-ou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745203/
https://www.ncbi.nlm.nih.gov/pubmed/35008707
http://dx.doi.org/10.3390/ijms23010281
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author Hsieh, Hao-Hsuan
Shan, Shu-ou
author_facet Hsieh, Hao-Hsuan
Shan, Shu-ou
author_sort Hsieh, Hao-Hsuan
collection PubMed
description Fidelity of protein targeting is essential for the proper biogenesis and functioning of organelles. Unlike replication, transcription and translation processes, in which multiple mechanisms to recognize and reject noncognate substrates are established in energetic and molecular detail, the mechanisms by which cells achieve a high fidelity in protein localization remain incompletely understood. Signal recognition particle (SRP), a conserved pathway to mediate the localization of membrane and secretory proteins to the appropriate cellular membrane, provides a paradigm to understand the molecular basis of protein localization in the cell. In this chapter, we review recent progress in deciphering the molecular mechanisms and substrate selection of the mammalian SRP pathway, with an emphasis on the key role of the cotranslational chaperone NAC in preventing protein mistargeting to the ER and in ensuring the organelle specificity of protein localization.
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spelling pubmed-87452032022-01-11 Fidelity of Cotranslational Protein Targeting to the Endoplasmic Reticulum Hsieh, Hao-Hsuan Shan, Shu-ou Int J Mol Sci Review Fidelity of protein targeting is essential for the proper biogenesis and functioning of organelles. Unlike replication, transcription and translation processes, in which multiple mechanisms to recognize and reject noncognate substrates are established in energetic and molecular detail, the mechanisms by which cells achieve a high fidelity in protein localization remain incompletely understood. Signal recognition particle (SRP), a conserved pathway to mediate the localization of membrane and secretory proteins to the appropriate cellular membrane, provides a paradigm to understand the molecular basis of protein localization in the cell. In this chapter, we review recent progress in deciphering the molecular mechanisms and substrate selection of the mammalian SRP pathway, with an emphasis on the key role of the cotranslational chaperone NAC in preventing protein mistargeting to the ER and in ensuring the organelle specificity of protein localization. MDPI 2021-12-28 /pmc/articles/PMC8745203/ /pubmed/35008707 http://dx.doi.org/10.3390/ijms23010281 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Hsieh, Hao-Hsuan
Shan, Shu-ou
Fidelity of Cotranslational Protein Targeting to the Endoplasmic Reticulum
title Fidelity of Cotranslational Protein Targeting to the Endoplasmic Reticulum
title_full Fidelity of Cotranslational Protein Targeting to the Endoplasmic Reticulum
title_fullStr Fidelity of Cotranslational Protein Targeting to the Endoplasmic Reticulum
title_full_unstemmed Fidelity of Cotranslational Protein Targeting to the Endoplasmic Reticulum
title_short Fidelity of Cotranslational Protein Targeting to the Endoplasmic Reticulum
title_sort fidelity of cotranslational protein targeting to the endoplasmic reticulum
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745203/
https://www.ncbi.nlm.nih.gov/pubmed/35008707
http://dx.doi.org/10.3390/ijms23010281
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