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A single amino acid change in the cytoplasmic domain alters the polarized delivery of influenza virus hemagglutinin
In the polarized kidney cell line MDCK, the influenza virus hemagglutinin (HA) has been well characterized as a model for apically sorted membrane glycoproteins. Previous work from our laboratory has shown that a single amino acid change in the cytoplasmic sequence of HA converts it from a protein t...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1991
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2289095/ https://www.ncbi.nlm.nih.gov/pubmed/1860878 |
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collection | PubMed |
description | In the polarized kidney cell line MDCK, the influenza virus hemagglutinin (HA) has been well characterized as a model for apically sorted membrane glycoproteins. Previous work from our laboratory has shown that a single amino acid change in the cytoplasmic sequence of HA converts it from a protein that is excluded from coated pits to one that is efficiently internalized. Using trypsin or antibodies to mark protein on the surface, we have shown in MDCK cells that HA containing this mutation is no longer transported to the apical surface but instead is delivered directly to the basolateral plasma membrane. We propose that a cytoplasmic feature similar to an endocytosis signal can cause exclusive basolateral delivery. |
format | Text |
id | pubmed-2289095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1991 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22890952008-05-01 A single amino acid change in the cytoplasmic domain alters the polarized delivery of influenza virus hemagglutinin J Cell Biol Articles In the polarized kidney cell line MDCK, the influenza virus hemagglutinin (HA) has been well characterized as a model for apically sorted membrane glycoproteins. Previous work from our laboratory has shown that a single amino acid change in the cytoplasmic sequence of HA converts it from a protein that is excluded from coated pits to one that is efficiently internalized. Using trypsin or antibodies to mark protein on the surface, we have shown in MDCK cells that HA containing this mutation is no longer transported to the apical surface but instead is delivered directly to the basolateral plasma membrane. We propose that a cytoplasmic feature similar to an endocytosis signal can cause exclusive basolateral delivery. The Rockefeller University Press 1991-08-01 /pmc/articles/PMC2289095/ /pubmed/1860878 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles A single amino acid change in the cytoplasmic domain alters the polarized delivery of influenza virus hemagglutinin |
title | A single amino acid change in the cytoplasmic domain alters the polarized delivery of influenza virus hemagglutinin |
title_full | A single amino acid change in the cytoplasmic domain alters the polarized delivery of influenza virus hemagglutinin |
title_fullStr | A single amino acid change in the cytoplasmic domain alters the polarized delivery of influenza virus hemagglutinin |
title_full_unstemmed | A single amino acid change in the cytoplasmic domain alters the polarized delivery of influenza virus hemagglutinin |
title_short | A single amino acid change in the cytoplasmic domain alters the polarized delivery of influenza virus hemagglutinin |
title_sort | single amino acid change in the cytoplasmic domain alters the polarized delivery of influenza virus hemagglutinin |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2289095/ https://www.ncbi.nlm.nih.gov/pubmed/1860878 |