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Chapter 6 Protein Sorting in the Secretory Pathway
This chapter focuses on protein sorting in the secretory pathway. From primary and secondary biosynthetic sites in the cytosol and mitochondrial matrix, respectively, proteins and lipids are distributed to more than 30 final destinations in membranes or membrane-bound spaces, where they carry out th...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academic Press Inc. Published by Elsevier Inc.
1985
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7146842/ https://www.ncbi.nlm.nih.gov/pubmed/32287478 http://dx.doi.org/10.1016/S0070-2161(08)60328-7 |
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author | Rodriguez-Boulan, Enrique Misek, David E. Salas, Dora Vega De Salas, Pedro J.I. Bard, Enzo |
author_facet | Rodriguez-Boulan, Enrique Misek, David E. Salas, Dora Vega De Salas, Pedro J.I. Bard, Enzo |
author_sort | Rodriguez-Boulan, Enrique |
collection | PubMed |
description | This chapter focuses on protein sorting in the secretory pathway. From primary and secondary biosynthetic sites in the cytosol and mitochondrial matrix, respectively, proteins and lipids are distributed to more than 30 final destinations in membranes or membrane-bound spaces, where they carry out their programmed function. Molecular sorting is defined, in its most general sense, as the sum of the mechanisms that determine the distribution of a given molecule from its site of synthesis to its site of function in the cell. The final site of residence of a protein in a eukaryotic cell is determined by a combination of various factors, acting in concert: (1) site of synthesis, (2) sorting signals or zip codes, (3) signal recognition or decoding mechanisms, (4) cotranslational or posttranslational mechanisms for translocation across membranes, (5) specific fusion–fission interactions between intracellular vesicular compartments, and (6) restrictions to the lateral mobility in the plane of the bilayer. Improvements in cell fractionation, protein separation, and immune precipitation procedures in the past decade have made them possible. Very little is known about the mechanisms that mediate the localization and concentration of specific proteins and lipids within organelles. Various experimental model systems have become available for their study. The advent of recombinant DNA technology has shortened the time needed for obtaining the primary structure of proteins to a few months. |
format | Online Article Text |
id | pubmed-7146842 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1985 |
publisher | Academic Press Inc. Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71468422020-04-10 Chapter 6 Protein Sorting in the Secretory Pathway Rodriguez-Boulan, Enrique Misek, David E. Salas, Dora Vega De Salas, Pedro J.I. Bard, Enzo Curr Top Membr Transp Article This chapter focuses on protein sorting in the secretory pathway. From primary and secondary biosynthetic sites in the cytosol and mitochondrial matrix, respectively, proteins and lipids are distributed to more than 30 final destinations in membranes or membrane-bound spaces, where they carry out their programmed function. Molecular sorting is defined, in its most general sense, as the sum of the mechanisms that determine the distribution of a given molecule from its site of synthesis to its site of function in the cell. The final site of residence of a protein in a eukaryotic cell is determined by a combination of various factors, acting in concert: (1) site of synthesis, (2) sorting signals or zip codes, (3) signal recognition or decoding mechanisms, (4) cotranslational or posttranslational mechanisms for translocation across membranes, (5) specific fusion–fission interactions between intracellular vesicular compartments, and (6) restrictions to the lateral mobility in the plane of the bilayer. Improvements in cell fractionation, protein separation, and immune precipitation procedures in the past decade have made them possible. Very little is known about the mechanisms that mediate the localization and concentration of specific proteins and lipids within organelles. Various experimental model systems have become available for their study. The advent of recombinant DNA technology has shortened the time needed for obtaining the primary structure of proteins to a few months. Academic Press Inc. Published by Elsevier Inc. 1985 2008-05-30 /pmc/articles/PMC7146842/ /pubmed/32287478 http://dx.doi.org/10.1016/S0070-2161(08)60328-7 Text en © 1985 Academic Press Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Rodriguez-Boulan, Enrique Misek, David E. Salas, Dora Vega De Salas, Pedro J.I. Bard, Enzo Chapter 6 Protein Sorting in the Secretory Pathway |
title | Chapter 6 Protein Sorting in the Secretory Pathway |
title_full | Chapter 6 Protein Sorting in the Secretory Pathway |
title_fullStr | Chapter 6 Protein Sorting in the Secretory Pathway |
title_full_unstemmed | Chapter 6 Protein Sorting in the Secretory Pathway |
title_short | Chapter 6 Protein Sorting in the Secretory Pathway |
title_sort | chapter 6 protein sorting in the secretory pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7146842/ https://www.ncbi.nlm.nih.gov/pubmed/32287478 http://dx.doi.org/10.1016/S0070-2161(08)60328-7 |
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