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Comparative studies of three cholesteryl ester transfer proteins and their interactions with known inhibitors
Cholesteryl ester transfer protein (CETP) is a plasma protein that mediates bidirectional transfers of cholesteryl esters and triglycerides between low-density lipoproteins and high-density lipoproteins (HDL). Because low levels of plasma CETP are associated with increased plasma HDL-cholesterol, th...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5540280/ https://www.ncbi.nlm.nih.gov/pubmed/28767652 http://dx.doi.org/10.1371/journal.pone.0180772 |
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author | Wang, Ziyun Niimi, Manabu Ding, Qianzhi Liu, Zhenming Wang, Ling Zhang, Jifeng Xu, Jun Fan, Jianglin |
author_facet | Wang, Ziyun Niimi, Manabu Ding, Qianzhi Liu, Zhenming Wang, Ling Zhang, Jifeng Xu, Jun Fan, Jianglin |
author_sort | Wang, Ziyun |
collection | PubMed |
description | Cholesteryl ester transfer protein (CETP) is a plasma protein that mediates bidirectional transfers of cholesteryl esters and triglycerides between low-density lipoproteins and high-density lipoproteins (HDL). Because low levels of plasma CETP are associated with increased plasma HDL-cholesterol, therapeutic inhibition of CETP activity is considered an attractive strategy for elevating plasma HDL-cholesterol, thereby hoping to reduce the risk of cardiovascular disease. Interestingly, only a few laboratory animals, such as rabbits, guinea pigs, and hamsters, have plasma CETP activity, whereas mice and rats do not. It is not known whether all CETPs in these laboratory animals are functionally similar to human CETP. In the current study, we compared plasma CETP activity and characterized the plasma lipoprotein profiles of these animals. Furthermore, we studied the three CETP molecular structures, physicochemical characteristics, and binding properties with known CETP inhibitors in silico. Our results showed that rabbits exhibited higher CETP activity than guinea pigs and hamsters, while these animals had different lipoprotein profiles. CETP inhibitors can inhibit rabbit and hamster CETP activity in a similar manner to human CETP. Analysis of CETP molecules in silico revealed that rabbit and hamster CETP showed many features that are similar to human CETP. These results provide novel insights into understanding CETP functions and molecular properties. |
format | Online Article Text |
id | pubmed-5540280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55402802017-08-12 Comparative studies of three cholesteryl ester transfer proteins and their interactions with known inhibitors Wang, Ziyun Niimi, Manabu Ding, Qianzhi Liu, Zhenming Wang, Ling Zhang, Jifeng Xu, Jun Fan, Jianglin PLoS One Research Article Cholesteryl ester transfer protein (CETP) is a plasma protein that mediates bidirectional transfers of cholesteryl esters and triglycerides between low-density lipoproteins and high-density lipoproteins (HDL). Because low levels of plasma CETP are associated with increased plasma HDL-cholesterol, therapeutic inhibition of CETP activity is considered an attractive strategy for elevating plasma HDL-cholesterol, thereby hoping to reduce the risk of cardiovascular disease. Interestingly, only a few laboratory animals, such as rabbits, guinea pigs, and hamsters, have plasma CETP activity, whereas mice and rats do not. It is not known whether all CETPs in these laboratory animals are functionally similar to human CETP. In the current study, we compared plasma CETP activity and characterized the plasma lipoprotein profiles of these animals. Furthermore, we studied the three CETP molecular structures, physicochemical characteristics, and binding properties with known CETP inhibitors in silico. Our results showed that rabbits exhibited higher CETP activity than guinea pigs and hamsters, while these animals had different lipoprotein profiles. CETP inhibitors can inhibit rabbit and hamster CETP activity in a similar manner to human CETP. Analysis of CETP molecules in silico revealed that rabbit and hamster CETP showed many features that are similar to human CETP. These results provide novel insights into understanding CETP functions and molecular properties. Public Library of Science 2017-08-02 /pmc/articles/PMC5540280/ /pubmed/28767652 http://dx.doi.org/10.1371/journal.pone.0180772 Text en © 2017 Wang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Wang, Ziyun Niimi, Manabu Ding, Qianzhi Liu, Zhenming Wang, Ling Zhang, Jifeng Xu, Jun Fan, Jianglin Comparative studies of three cholesteryl ester transfer proteins and their interactions with known inhibitors |
title | Comparative studies of three cholesteryl ester transfer proteins and their interactions with known inhibitors |
title_full | Comparative studies of three cholesteryl ester transfer proteins and their interactions with known inhibitors |
title_fullStr | Comparative studies of three cholesteryl ester transfer proteins and their interactions with known inhibitors |
title_full_unstemmed | Comparative studies of three cholesteryl ester transfer proteins and their interactions with known inhibitors |
title_short | Comparative studies of three cholesteryl ester transfer proteins and their interactions with known inhibitors |
title_sort | comparative studies of three cholesteryl ester transfer proteins and their interactions with known inhibitors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5540280/ https://www.ncbi.nlm.nih.gov/pubmed/28767652 http://dx.doi.org/10.1371/journal.pone.0180772 |
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