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Identification of NPC1 as the target of U18666A, an inhibitor of lysosomal cholesterol export and Ebola infection
Niemann-Pick C1 (NPC1) is a lysosomal membrane protein that exports cholesterol derived from receptor-mediated uptake of LDL, and it also mediates cellular entry of Ebola virus. Cholesterol export is inhibited by nanomolar concentrations of U18666A, a cationic sterol. To identify the target of U1866...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4718804/ https://www.ncbi.nlm.nih.gov/pubmed/26646182 http://dx.doi.org/10.7554/eLife.12177 |
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author | Lu, Feiran Liang, Qiren Abi-Mosleh, Lina Das, Akash De Brabander, Jef K Goldstein, Joseph L Brown, Michael S |
author_facet | Lu, Feiran Liang, Qiren Abi-Mosleh, Lina Das, Akash De Brabander, Jef K Goldstein, Joseph L Brown, Michael S |
author_sort | Lu, Feiran |
collection | PubMed |
description | Niemann-Pick C1 (NPC1) is a lysosomal membrane protein that exports cholesterol derived from receptor-mediated uptake of LDL, and it also mediates cellular entry of Ebola virus. Cholesterol export is inhibited by nanomolar concentrations of U18666A, a cationic sterol. To identify the target of U18666A, we synthesized U-X, a U18666A derivative with a benzophenone that permits ultraviolet-induced crosslinking. When added to CHO cells, U-X crosslinked to NPC1. Crosslinking was blocked by U18666A derivatives that block cholesterol export, but not derivatives lacking blocking activity. Crosslinking was prevented by point mutation in the sterol-sensing domain (SSD) of NPC1, but not by point mutation in the N-terminal domain (NTD). These data suggest that the SSD contains a U18666A-inhibitable site required for cholesterol export distinct from the cholesterol-binding site in the NTD. Inasmuch as inhibition of Ebola requires 100-fold higher concentrations of U18666A, the high affinity U16888A-binding site is likely not required for virus entry. DOI: http://dx.doi.org/10.7554/eLife.12177.001 |
format | Online Article Text |
id | pubmed-4718804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47188042016-01-21 Identification of NPC1 as the target of U18666A, an inhibitor of lysosomal cholesterol export and Ebola infection Lu, Feiran Liang, Qiren Abi-Mosleh, Lina Das, Akash De Brabander, Jef K Goldstein, Joseph L Brown, Michael S eLife Biochemistry Niemann-Pick C1 (NPC1) is a lysosomal membrane protein that exports cholesterol derived from receptor-mediated uptake of LDL, and it also mediates cellular entry of Ebola virus. Cholesterol export is inhibited by nanomolar concentrations of U18666A, a cationic sterol. To identify the target of U18666A, we synthesized U-X, a U18666A derivative with a benzophenone that permits ultraviolet-induced crosslinking. When added to CHO cells, U-X crosslinked to NPC1. Crosslinking was blocked by U18666A derivatives that block cholesterol export, but not derivatives lacking blocking activity. Crosslinking was prevented by point mutation in the sterol-sensing domain (SSD) of NPC1, but not by point mutation in the N-terminal domain (NTD). These data suggest that the SSD contains a U18666A-inhibitable site required for cholesterol export distinct from the cholesterol-binding site in the NTD. Inasmuch as inhibition of Ebola requires 100-fold higher concentrations of U18666A, the high affinity U16888A-binding site is likely not required for virus entry. DOI: http://dx.doi.org/10.7554/eLife.12177.001 eLife Sciences Publications, Ltd 2015-12-08 /pmc/articles/PMC4718804/ /pubmed/26646182 http://dx.doi.org/10.7554/eLife.12177 Text en © 2015, Lu et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry Lu, Feiran Liang, Qiren Abi-Mosleh, Lina Das, Akash De Brabander, Jef K Goldstein, Joseph L Brown, Michael S Identification of NPC1 as the target of U18666A, an inhibitor of lysosomal cholesterol export and Ebola infection |
title | Identification of NPC1 as the target of U18666A, an inhibitor of lysosomal cholesterol export and Ebola infection |
title_full | Identification of NPC1 as the target of U18666A, an inhibitor of lysosomal cholesterol export and Ebola infection |
title_fullStr | Identification of NPC1 as the target of U18666A, an inhibitor of lysosomal cholesterol export and Ebola infection |
title_full_unstemmed | Identification of NPC1 as the target of U18666A, an inhibitor of lysosomal cholesterol export and Ebola infection |
title_short | Identification of NPC1 as the target of U18666A, an inhibitor of lysosomal cholesterol export and Ebola infection |
title_sort | identification of npc1 as the target of u18666a, an inhibitor of lysosomal cholesterol export and ebola infection |
topic | Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4718804/ https://www.ncbi.nlm.nih.gov/pubmed/26646182 http://dx.doi.org/10.7554/eLife.12177 |
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