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Drug Rescue Distinguishes between Different Structural Models of Human P-Glycoprotein
[Image: see text] There is no high-resolution crystal structure of the human P-glycoprotein (P-gp) drug pump. Homology models of human P-gp based on the crystal structures of mouse or Caenorhabditis elegans P-gps show large differences in the orientation of transmembrane segment 5 (TM5). TM5 is one...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3798097/ https://www.ncbi.nlm.nih.gov/pubmed/24083983 http://dx.doi.org/10.1021/bi401269m |
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author | Loo, Tip W. Clarke, David M. |
author_facet | Loo, Tip W. Clarke, David M. |
author_sort | Loo, Tip W. |
collection | PubMed |
description | [Image: see text] There is no high-resolution crystal structure of the human P-glycoprotein (P-gp) drug pump. Homology models of human P-gp based on the crystal structures of mouse or Caenorhabditis elegans P-gps show large differences in the orientation of transmembrane segment 5 (TM5). TM5 is one of the most important transmembrane segments involved in drug–substrate interactions. Drug rescue of P-gp processing mutants containing an arginine at each position in TM5 was used to identify positions facing the lipid or internal aqueous chamber. Only the model based on the C. elegans P-gp structure was compatible with the drug rescue results. |
format | Online Article Text |
id | pubmed-3798097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-37980972013-10-18 Drug Rescue Distinguishes between Different Structural Models of Human P-Glycoprotein Loo, Tip W. Clarke, David M. Biochemistry [Image: see text] There is no high-resolution crystal structure of the human P-glycoprotein (P-gp) drug pump. Homology models of human P-gp based on the crystal structures of mouse or Caenorhabditis elegans P-gps show large differences in the orientation of transmembrane segment 5 (TM5). TM5 is one of the most important transmembrane segments involved in drug–substrate interactions. Drug rescue of P-gp processing mutants containing an arginine at each position in TM5 was used to identify positions facing the lipid or internal aqueous chamber. Only the model based on the C. elegans P-gp structure was compatible with the drug rescue results. American Chemical Society 2013-10-01 2013-10-15 /pmc/articles/PMC3798097/ /pubmed/24083983 http://dx.doi.org/10.1021/bi401269m Text en Copyright © 2013 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) |
spellingShingle | Loo, Tip W. Clarke, David M. Drug Rescue Distinguishes between Different Structural Models of Human P-Glycoprotein |
title | Drug Rescue Distinguishes between Different Structural Models of Human P-Glycoprotein |
title_full | Drug Rescue Distinguishes between Different Structural Models of Human P-Glycoprotein |
title_fullStr | Drug Rescue Distinguishes between Different Structural Models of Human P-Glycoprotein |
title_full_unstemmed | Drug Rescue Distinguishes between Different Structural Models of Human P-Glycoprotein |
title_short | Drug Rescue Distinguishes between Different Structural Models of Human P-Glycoprotein |
title_sort | drug rescue distinguishes between different structural models of human p-glycoprotein |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3798097/ https://www.ncbi.nlm.nih.gov/pubmed/24083983 http://dx.doi.org/10.1021/bi401269m |
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