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Cell membrane chromatography for the analysis of the interaction between chloroquine and hydroxychloroquine with ACE2 receptors

The recent emergence of the novel pathogenic coronavirus disease 2019 (COVID-19) is responsible for a worldwide pandemic. In sight of this, there has been growing interest in the use of chloroquine (CQ) and hydroxychloroquine (HCQ) as potential treatments. In this study, we use angiotensin convertin...

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Detalles Bibliográficos
Autores principales: Fu, Jia, Jia, Qianqian, Zhou, Huaxin, Zhang, Liyang, Wang, Saisai, Liang, Peida, Lv, Yanni, Han, Shengli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700726/
https://www.ncbi.nlm.nih.gov/pubmed/33310480
http://dx.doi.org/10.1016/j.jchromb.2020.122469
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author Fu, Jia
Jia, Qianqian
Zhou, Huaxin
Zhang, Liyang
Wang, Saisai
Liang, Peida
Lv, Yanni
Han, Shengli
author_facet Fu, Jia
Jia, Qianqian
Zhou, Huaxin
Zhang, Liyang
Wang, Saisai
Liang, Peida
Lv, Yanni
Han, Shengli
author_sort Fu, Jia
collection PubMed
description The recent emergence of the novel pathogenic coronavirus disease 2019 (COVID-19) is responsible for a worldwide pandemic. In sight of this, there has been growing interest in the use of chloroquine (CQ) and hydroxychloroquine (HCQ) as potential treatments. In this study, we use angiotensin converting enzyme 2 (ACE2) over-expressed cell membrane chromatography (CMC) to study the interaction of CQ and HCQ with ACE2 receptor. Both CQ and HCQ were retained on the ACE2/CMC column. Then we analyzed the binding character of CQ and HCQ to ACE2 by CMC frontal analysis, ionic force investigation and competitive binding experiment. Results showed that CQ and HCQ KD values obtained from the CMC frontal analysis method were 8.22(±0.61) × 10(−7) M and 11.70(±2.44) × 10(−7) M. Compare to CQ, HCQ has the weaker affinity with ACE2. The action force of CQ, HCQ and ACE2 is mainly ionic force. CQ and HCQ have different degrees of competitive binding relationship with ACE2. Our study revealed the interaction of CQ and HCQ with ACE2 receptor, which provides new insights for the use of CQ and HCQ in the treatment of COVID-19. Moreover, this biomimetic drug screening method is expected to open the door for rapid targeting and separating bioactive ingredients active towards ACE2 receptor.
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spelling pubmed-77007262020-12-01 Cell membrane chromatography for the analysis of the interaction between chloroquine and hydroxychloroquine with ACE2 receptors Fu, Jia Jia, Qianqian Zhou, Huaxin Zhang, Liyang Wang, Saisai Liang, Peida Lv, Yanni Han, Shengli J Chromatogr B Analyt Technol Biomed Life Sci Short Communication The recent emergence of the novel pathogenic coronavirus disease 2019 (COVID-19) is responsible for a worldwide pandemic. In sight of this, there has been growing interest in the use of chloroquine (CQ) and hydroxychloroquine (HCQ) as potential treatments. In this study, we use angiotensin converting enzyme 2 (ACE2) over-expressed cell membrane chromatography (CMC) to study the interaction of CQ and HCQ with ACE2 receptor. Both CQ and HCQ were retained on the ACE2/CMC column. Then we analyzed the binding character of CQ and HCQ to ACE2 by CMC frontal analysis, ionic force investigation and competitive binding experiment. Results showed that CQ and HCQ KD values obtained from the CMC frontal analysis method were 8.22(±0.61) × 10(−7) M and 11.70(±2.44) × 10(−7) M. Compare to CQ, HCQ has the weaker affinity with ACE2. The action force of CQ, HCQ and ACE2 is mainly ionic force. CQ and HCQ have different degrees of competitive binding relationship with ACE2. Our study revealed the interaction of CQ and HCQ with ACE2 receptor, which provides new insights for the use of CQ and HCQ in the treatment of COVID-19. Moreover, this biomimetic drug screening method is expected to open the door for rapid targeting and separating bioactive ingredients active towards ACE2 receptor. Elsevier B.V. 2021-01-01 2020-11-29 /pmc/articles/PMC7700726/ /pubmed/33310480 http://dx.doi.org/10.1016/j.jchromb.2020.122469 Text en © 2020 Elsevier B.V. All rights reserved. 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 Short Communication
Fu, Jia
Jia, Qianqian
Zhou, Huaxin
Zhang, Liyang
Wang, Saisai
Liang, Peida
Lv, Yanni
Han, Shengli
Cell membrane chromatography for the analysis of the interaction between chloroquine and hydroxychloroquine with ACE2 receptors
title Cell membrane chromatography for the analysis of the interaction between chloroquine and hydroxychloroquine with ACE2 receptors
title_full Cell membrane chromatography for the analysis of the interaction between chloroquine and hydroxychloroquine with ACE2 receptors
title_fullStr Cell membrane chromatography for the analysis of the interaction between chloroquine and hydroxychloroquine with ACE2 receptors
title_full_unstemmed Cell membrane chromatography for the analysis of the interaction between chloroquine and hydroxychloroquine with ACE2 receptors
title_short Cell membrane chromatography for the analysis of the interaction between chloroquine and hydroxychloroquine with ACE2 receptors
title_sort cell membrane chromatography for the analysis of the interaction between chloroquine and hydroxychloroquine with ace2 receptors
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700726/
https://www.ncbi.nlm.nih.gov/pubmed/33310480
http://dx.doi.org/10.1016/j.jchromb.2020.122469
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