Investigation of Interaction between the Spike Protein of SARS-CoV-2 and ACE2-Expressing Cells Using an In Vitro Cell Capturing System

Abstract Background The Interaction between severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein with Angiotensin converting enzyme 2 (ACE2) on the host cells is a crucial step for the viral entry and infection. Therefore, investigating the molecular mechanism underlying the in...

Full description

Bibliographic Details
Main Authors: Yuning Shang, Feixiang Chen, Shasha Li, Lijuan Song, Yunzhen Gao, Xinhua Yu, Junfeng Zheng
Format: Article
Language:English
Published: BMC 2021-08-01
Series:Biological Procedures Online
Subjects:
Online Access:https://doi.org/10.1186/s12575-021-00153-9
_version_ 1819120928678739968
author Yuning Shang
Feixiang Chen
Shasha Li
Lijuan Song
Yunzhen Gao
Xinhua Yu
Junfeng Zheng
author_facet Yuning Shang
Feixiang Chen
Shasha Li
Lijuan Song
Yunzhen Gao
Xinhua Yu
Junfeng Zheng
author_sort Yuning Shang
collection DOAJ
description Abstract Background The Interaction between severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein with Angiotensin converting enzyme 2 (ACE2) on the host cells is a crucial step for the viral entry and infection. Therefore, investigating the molecular mechanism underlying the interaction is of great importance for the prevention of the infection of SARS-CoV-2. In this study, we aimed to establish a virus-free in vitro system to study the interaction between the spike protein and host cells of SARS-CoV-2. Results Our results show that ACE2-overexpressing HEK293T cells are captured by immobilized spike S1 protein, and the cell capturing process can be inhibited by the receptor binding domain of the spike protein or antibodies against S protein. Furthermore, spike S1 protein variant with D614G mutant show a higher cell capturing ability than wild type spike S1 protein and stronger binding capacity of its receptor ACE2. In addition, the captured cells can be eluted as living cells for further investigation. Conclusions This study provides a new in vitro system for investigating the interaction between SARS-CoV-2 and host cells and purifying ACE2-expressing cells.
first_indexed 2024-12-22T06:28:28Z
format Article
id doaj.art-4db7c1b72dce4363a84ae6302bb2a7ef
institution Directory Open Access Journal
issn 1480-9222
language English
last_indexed 2024-12-22T06:28:28Z
publishDate 2021-08-01
publisher BMC
record_format Article
series Biological Procedures Online
spelling doaj.art-4db7c1b72dce4363a84ae6302bb2a7ef2022-12-21T18:35:47ZengBMCBiological Procedures Online1480-92222021-08-012311910.1186/s12575-021-00153-9Investigation of Interaction between the Spike Protein of SARS-CoV-2 and ACE2-Expressing Cells Using an In Vitro Cell Capturing SystemYuning Shang0Feixiang Chen1Shasha Li2Lijuan Song3Yunzhen Gao4Xinhua Yu5Junfeng Zheng6Institute of Psychiatry and Neuroscience, Xinxiang Medical UniversityInstitute of Psychiatry and Neuroscience, Xinxiang Medical UniversityInstitute of Psychiatry and Neuroscience, Xinxiang Medical UniversityInstitute of Psychiatry and Neuroscience, Xinxiang Medical UniversityInstitute of Psychiatry and Neuroscience, Xinxiang Medical UniversityPriority Area Asthma & Allergy, Research Center Borstel, Airway Research Center North (ARCN), Members of the German Center for Lung Research (DZL)Institute of Psychiatry and Neuroscience, Xinxiang Medical UniversityAbstract Background The Interaction between severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein with Angiotensin converting enzyme 2 (ACE2) on the host cells is a crucial step for the viral entry and infection. Therefore, investigating the molecular mechanism underlying the interaction is of great importance for the prevention of the infection of SARS-CoV-2. In this study, we aimed to establish a virus-free in vitro system to study the interaction between the spike protein and host cells of SARS-CoV-2. Results Our results show that ACE2-overexpressing HEK293T cells are captured by immobilized spike S1 protein, and the cell capturing process can be inhibited by the receptor binding domain of the spike protein or antibodies against S protein. Furthermore, spike S1 protein variant with D614G mutant show a higher cell capturing ability than wild type spike S1 protein and stronger binding capacity of its receptor ACE2. In addition, the captured cells can be eluted as living cells for further investigation. Conclusions This study provides a new in vitro system for investigating the interaction between SARS-CoV-2 and host cells and purifying ACE2-expressing cells.https://doi.org/10.1186/s12575-021-00153-9SARS-CoV-2;spike proteinACE2In vitro cell-capture
spellingShingle Yuning Shang
Feixiang Chen
Shasha Li
Lijuan Song
Yunzhen Gao
Xinhua Yu
Junfeng Zheng
Investigation of Interaction between the Spike Protein of SARS-CoV-2 and ACE2-Expressing Cells Using an In Vitro Cell Capturing System
Biological Procedures Online
SARS-CoV-2;spike protein
ACE2
In vitro cell-capture
title Investigation of Interaction between the Spike Protein of SARS-CoV-2 and ACE2-Expressing Cells Using an In Vitro Cell Capturing System
title_full Investigation of Interaction between the Spike Protein of SARS-CoV-2 and ACE2-Expressing Cells Using an In Vitro Cell Capturing System
title_fullStr Investigation of Interaction between the Spike Protein of SARS-CoV-2 and ACE2-Expressing Cells Using an In Vitro Cell Capturing System
title_full_unstemmed Investigation of Interaction between the Spike Protein of SARS-CoV-2 and ACE2-Expressing Cells Using an In Vitro Cell Capturing System
title_short Investigation of Interaction between the Spike Protein of SARS-CoV-2 and ACE2-Expressing Cells Using an In Vitro Cell Capturing System
title_sort investigation of interaction between the spike protein of sars cov 2 and ace2 expressing cells using an in vitro cell capturing system
topic SARS-CoV-2;spike protein
ACE2
In vitro cell-capture
url https://doi.org/10.1186/s12575-021-00153-9
work_keys_str_mv AT yuningshang investigationofinteractionbetweenthespikeproteinofsarscov2andace2expressingcellsusinganinvitrocellcapturingsystem
AT feixiangchen investigationofinteractionbetweenthespikeproteinofsarscov2andace2expressingcellsusinganinvitrocellcapturingsystem
AT shashali investigationofinteractionbetweenthespikeproteinofsarscov2andace2expressingcellsusinganinvitrocellcapturingsystem
AT lijuansong investigationofinteractionbetweenthespikeproteinofsarscov2andace2expressingcellsusinganinvitrocellcapturingsystem
AT yunzhengao investigationofinteractionbetweenthespikeproteinofsarscov2andace2expressingcellsusinganinvitrocellcapturingsystem
AT xinhuayu investigationofinteractionbetweenthespikeproteinofsarscov2andace2expressingcellsusinganinvitrocellcapturingsystem
AT junfengzheng investigationofinteractionbetweenthespikeproteinofsarscov2andace2expressingcellsusinganinvitrocellcapturingsystem