Loading…
Human H-ferritin presenting RBM of spike glycoprotein as potential vaccine of SARS-CoV-2
The outbreak of COVID-19 has so far inflicted millions of people all around the world and will have a long lasting effect on every aspect of everyone's life. Yet there is no effective approved treatment for the disease. In an effort of utilizing human ferritin as nanoplatform for drug delivery,...
Saved in:
Published in: | bioRxiv 2020-06 |
---|---|
Main Authors: | , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Request full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-b1528-c43895f489404c3d6881d4e2c96753af77a24173bf155c220c89daa9a0ceb4e03 |
---|---|
cites | |
container_end_page | |
container_issue | |
container_start_page | |
container_title | bioRxiv |
container_volume | |
creator | Yao, Dehui Lao, Fang Zhang, Zeyi Liu, Yan Cheng, Jianwei Ding, Fengjiao Wang, Xiaofei Lun Xi Wang, Chuang Xichong Yan Zhang, Rongkun Ouyang, Fangxing Ding, Hui Ke, Tianyi |
description | The outbreak of COVID-19 has so far inflicted millions of people all around the world and will have a long lasting effect on every aspect of everyone's life. Yet there is no effective approved treatment for the disease. In an effort of utilizing human ferritin as nanoplatform for drug delivery, we engineered a fusion protein by presenting receptor-binding motif (RBM) of SARS-CoV-2 virus spike glycoprotein on the N-terminus of ferritin subunits. The designed fusion protein with a cage-like structure, similar to that of corona virus, is a potential anti-SARS-CoV-2 vaccine. We hereby show the construction, preparation, and characterization of the fusion protein RBM-HFtn. Our initial affinity study confirmed its biological activity towards ACE2 receptor which suggests its mode of action against SARS-CoV-2 could be either through vaccine therapy or blocking the cellular entry of virus as antagonist of ACE2 receptor. Competing Interest Statement T. Ke holds ownership interest (including patents) in Kunshan Xinyunda Biotech Co., Ltd. No potential conflicts of interests were disclosed by the other authors. Footnotes * More authors were added to reflect their contribution to this work. |
doi_str_mv | 10.1101/2020.05.25.115618 |
format | article |
fullrecord | <record><control><sourceid>proquest_COVID</sourceid><recordid>TN_cdi_proquest_journals_2410538752</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2410538752</sourcerecordid><originalsourceid>FETCH-LOGICAL-b1528-c43895f489404c3d6881d4e2c96753af77a24173bf155c220c89daa9a0ceb4e03</originalsourceid><addsrcrecordid>eNotkEFLAzEQhYMgWGp_gLeAFy-pk0mymz3WolaoCK2KtyWbzZbUdndN2mL_vSn1NG_gY96bR8gNhzHnwO8REMagxqjSrjKuL8gAswKZRlBXZBTjGgCwyLjI5YB8zfZb09IZa1wIfudb2gcXXZvUii4eXmnX0Nj7b0dXm6Pt-tDtXIJMpH1SCTMbejDW-tad0OVksWTT7pPhNblszCa60f8cko-nx_fpjM3fnl-mkzmruELNrBS6UI3UhQRpRZ1pzWvp0BZZroRp8tyg5LmoGq6URQSri9qYwoB1lXQghuTufLfyXfj1h7IPfmvCsTwVUYIqUZXnIhJ6e0bTFz97F3flutuHNqUrkwcooXOF4g-mA11y</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2410538752</pqid></control><display><type>article</type><title>Human H-ferritin presenting RBM of spike glycoprotein as potential vaccine of SARS-CoV-2</title><source>Coronavirus Research Database</source><creator>Yao, Dehui ; Lao, Fang ; Zhang, Zeyi ; Liu, Yan ; Cheng, Jianwei ; Ding, Fengjiao ; Wang, Xiaofei ; Lun Xi ; Wang, Chuang ; Xichong Yan ; Zhang, Rongkun ; Ouyang, Fangxing ; Ding, Hui ; Ke, Tianyi</creator><creatorcontrib>Yao, Dehui ; Lao, Fang ; Zhang, Zeyi ; Liu, Yan ; Cheng, Jianwei ; Ding, Fengjiao ; Wang, Xiaofei ; Lun Xi ; Wang, Chuang ; Xichong Yan ; Zhang, Rongkun ; Ouyang, Fangxing ; Ding, Hui ; Ke, Tianyi</creatorcontrib><description>The outbreak of COVID-19 has so far inflicted millions of people all around the world and will have a long lasting effect on every aspect of everyone's life. Yet there is no effective approved treatment for the disease. In an effort of utilizing human ferritin as nanoplatform for drug delivery, we engineered a fusion protein by presenting receptor-binding motif (RBM) of SARS-CoV-2 virus spike glycoprotein on the N-terminus of ferritin subunits. The designed fusion protein with a cage-like structure, similar to that of corona virus, is a potential anti-SARS-CoV-2 vaccine. We hereby show the construction, preparation, and characterization of the fusion protein RBM-HFtn. Our initial affinity study confirmed its biological activity towards ACE2 receptor which suggests its mode of action against SARS-CoV-2 could be either through vaccine therapy or blocking the cellular entry of virus as antagonist of ACE2 receptor. Competing Interest Statement T. Ke holds ownership interest (including patents) in Kunshan Xinyunda Biotech Co., Ltd. No potential conflicts of interests were disclosed by the other authors. Footnotes * More authors were added to reflect their contribution to this work.</description><edition>1.2</edition><identifier>EISSN: 2692-8205</identifier><identifier>DOI: 10.1101/2020.05.25.115618</identifier><language>eng</language><publisher>Cold Spring Harbor: Cold Spring Harbor Laboratory Press</publisher><subject>ACE2 ; Angiotensin-converting enzyme 2 ; Bioengineering ; Biological activity ; Coronaviruses ; COVID-19 ; Drug delivery ; Ferritin ; Fusion protein ; Glycoproteins ; N-Terminus ; Protein structure ; Proteins ; Severe acute respiratory syndrome coronavirus 2 ; Spike glycoprotein ; Vaccines</subject><ispartof>bioRxiv, 2020-06</ispartof><rights>2020. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (“the License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020, Posted by Cold Spring Harbor Laboratory</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b1528-c43895f489404c3d6881d4e2c96753af77a24173bf155c220c89daa9a0ceb4e03</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2410538752?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,780,784,885,27923,38514,43893</link.rule.ids><linktorsrc>$$Uhttps://www.proquest.com/docview/2410538752?pq-origsite=primo$$EView_record_in_ProQuest$$FView_record_in_$$GProQuest$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Yao, Dehui</creatorcontrib><creatorcontrib>Lao, Fang</creatorcontrib><creatorcontrib>Zhang, Zeyi</creatorcontrib><creatorcontrib>Liu, Yan</creatorcontrib><creatorcontrib>Cheng, Jianwei</creatorcontrib><creatorcontrib>Ding, Fengjiao</creatorcontrib><creatorcontrib>Wang, Xiaofei</creatorcontrib><creatorcontrib>Lun Xi</creatorcontrib><creatorcontrib>Wang, Chuang</creatorcontrib><creatorcontrib>Xichong Yan</creatorcontrib><creatorcontrib>Zhang, Rongkun</creatorcontrib><creatorcontrib>Ouyang, Fangxing</creatorcontrib><creatorcontrib>Ding, Hui</creatorcontrib><creatorcontrib>Ke, Tianyi</creatorcontrib><title>Human H-ferritin presenting RBM of spike glycoprotein as potential vaccine of SARS-CoV-2</title><title>bioRxiv</title><description>The outbreak of COVID-19 has so far inflicted millions of people all around the world and will have a long lasting effect on every aspect of everyone's life. Yet there is no effective approved treatment for the disease. In an effort of utilizing human ferritin as nanoplatform for drug delivery, we engineered a fusion protein by presenting receptor-binding motif (RBM) of SARS-CoV-2 virus spike glycoprotein on the N-terminus of ferritin subunits. The designed fusion protein with a cage-like structure, similar to that of corona virus, is a potential anti-SARS-CoV-2 vaccine. We hereby show the construction, preparation, and characterization of the fusion protein RBM-HFtn. Our initial affinity study confirmed its biological activity towards ACE2 receptor which suggests its mode of action against SARS-CoV-2 could be either through vaccine therapy or blocking the cellular entry of virus as antagonist of ACE2 receptor. Competing Interest Statement T. Ke holds ownership interest (including patents) in Kunshan Xinyunda Biotech Co., Ltd. No potential conflicts of interests were disclosed by the other authors. Footnotes * More authors were added to reflect their contribution to this work.</description><subject>ACE2</subject><subject>Angiotensin-converting enzyme 2</subject><subject>Bioengineering</subject><subject>Biological activity</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>Drug delivery</subject><subject>Ferritin</subject><subject>Fusion protein</subject><subject>Glycoproteins</subject><subject>N-Terminus</subject><subject>Protein structure</subject><subject>Proteins</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Spike glycoprotein</subject><subject>Vaccines</subject><issn>2692-8205</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>COVID</sourceid><sourceid>PIMPY</sourceid><recordid>eNotkEFLAzEQhYMgWGp_gLeAFy-pk0mymz3WolaoCK2KtyWbzZbUdndN2mL_vSn1NG_gY96bR8gNhzHnwO8REMagxqjSrjKuL8gAswKZRlBXZBTjGgCwyLjI5YB8zfZb09IZa1wIfudb2gcXXZvUii4eXmnX0Nj7b0dXm6Pt-tDtXIJMpH1SCTMbejDW-tad0OVksWTT7pPhNblszCa60f8cko-nx_fpjM3fnl-mkzmruELNrBS6UI3UhQRpRZ1pzWvp0BZZroRp8tyg5LmoGq6URQSri9qYwoB1lXQghuTufLfyXfj1h7IPfmvCsTwVUYIqUZXnIhJ6e0bTFz97F3flutuHNqUrkwcooXOF4g-mA11y</recordid><startdate>20200608</startdate><enddate>20200608</enddate><creator>Yao, Dehui</creator><creator>Lao, Fang</creator><creator>Zhang, Zeyi</creator><creator>Liu, Yan</creator><creator>Cheng, Jianwei</creator><creator>Ding, Fengjiao</creator><creator>Wang, Xiaofei</creator><creator>Lun Xi</creator><creator>Wang, Chuang</creator><creator>Xichong Yan</creator><creator>Zhang, Rongkun</creator><creator>Ouyang, Fangxing</creator><creator>Ding, Hui</creator><creator>Ke, Tianyi</creator><general>Cold Spring Harbor Laboratory Press</general><general>Cold Spring Harbor Laboratory</general><scope>8FE</scope><scope>8FH</scope><scope>AAFGM</scope><scope>AAMXL</scope><scope>ABOIG</scope><scope>ABUWG</scope><scope>ADZZV</scope><scope>AFKRA</scope><scope>AFLLJ</scope><scope>AFOLM</scope><scope>AGAJT</scope><scope>AQTIP</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>COVID</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQCXX</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>FX.</scope></search><sort><creationdate>20200608</creationdate><title>Human H-ferritin presenting RBM of spike glycoprotein as potential vaccine of SARS-CoV-2</title><author>Yao, Dehui ; Lao, Fang ; Zhang, Zeyi ; Liu, Yan ; Cheng, Jianwei ; Ding, Fengjiao ; Wang, Xiaofei ; Lun Xi ; Wang, Chuang ; Xichong Yan ; Zhang, Rongkun ; Ouyang, Fangxing ; Ding, Hui ; Ke, Tianyi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1528-c43895f489404c3d6881d4e2c96753af77a24173bf155c220c89daa9a0ceb4e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>ACE2</topic><topic>Angiotensin-converting enzyme 2</topic><topic>Bioengineering</topic><topic>Biological activity</topic><topic>Coronaviruses</topic><topic>COVID-19</topic><topic>Drug delivery</topic><topic>Ferritin</topic><topic>Fusion protein</topic><topic>Glycoproteins</topic><topic>N-Terminus</topic><topic>Protein structure</topic><topic>Proteins</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Spike glycoprotein</topic><topic>Vaccines</topic><toplevel>online_resources</toplevel><creatorcontrib>Yao, Dehui</creatorcontrib><creatorcontrib>Lao, Fang</creatorcontrib><creatorcontrib>Zhang, Zeyi</creatorcontrib><creatorcontrib>Liu, Yan</creatorcontrib><creatorcontrib>Cheng, Jianwei</creatorcontrib><creatorcontrib>Ding, Fengjiao</creatorcontrib><creatorcontrib>Wang, Xiaofei</creatorcontrib><creatorcontrib>Lun Xi</creatorcontrib><creatorcontrib>Wang, Chuang</creatorcontrib><creatorcontrib>Xichong Yan</creatorcontrib><creatorcontrib>Zhang, Rongkun</creatorcontrib><creatorcontrib>Ouyang, Fangxing</creatorcontrib><creatorcontrib>Ding, Hui</creatorcontrib><creatorcontrib>Ke, Tianyi</creatorcontrib><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>Coronavirus Research Database</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>Biological Sciences</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>bioRxiv</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Yao, Dehui</au><au>Lao, Fang</au><au>Zhang, Zeyi</au><au>Liu, Yan</au><au>Cheng, Jianwei</au><au>Ding, Fengjiao</au><au>Wang, Xiaofei</au><au>Lun Xi</au><au>Wang, Chuang</au><au>Xichong Yan</au><au>Zhang, Rongkun</au><au>Ouyang, Fangxing</au><au>Ding, Hui</au><au>Ke, Tianyi</au><format>book</format><genre>document</genre><ristype>GEN</ristype><atitle>Human H-ferritin presenting RBM of spike glycoprotein as potential vaccine of SARS-CoV-2</atitle><jtitle>bioRxiv</jtitle><date>2020-06-08</date><risdate>2020</risdate><eissn>2692-8205</eissn><abstract>The outbreak of COVID-19 has so far inflicted millions of people all around the world and will have a long lasting effect on every aspect of everyone's life. Yet there is no effective approved treatment for the disease. In an effort of utilizing human ferritin as nanoplatform for drug delivery, we engineered a fusion protein by presenting receptor-binding motif (RBM) of SARS-CoV-2 virus spike glycoprotein on the N-terminus of ferritin subunits. The designed fusion protein with a cage-like structure, similar to that of corona virus, is a potential anti-SARS-CoV-2 vaccine. We hereby show the construction, preparation, and characterization of the fusion protein RBM-HFtn. Our initial affinity study confirmed its biological activity towards ACE2 receptor which suggests its mode of action against SARS-CoV-2 could be either through vaccine therapy or blocking the cellular entry of virus as antagonist of ACE2 receptor. Competing Interest Statement T. Ke holds ownership interest (including patents) in Kunshan Xinyunda Biotech Co., Ltd. No potential conflicts of interests were disclosed by the other authors. Footnotes * More authors were added to reflect their contribution to this work.</abstract><cop>Cold Spring Harbor</cop><pub>Cold Spring Harbor Laboratory Press</pub><doi>10.1101/2020.05.25.115618</doi><tpages>17</tpages><edition>1.2</edition><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | EISSN: 2692-8205 |
ispartof | bioRxiv, 2020-06 |
issn | 2692-8205 |
language | eng |
recordid | cdi_proquest_journals_2410538752 |
source | Coronavirus Research Database |
subjects | ACE2 Angiotensin-converting enzyme 2 Bioengineering Biological activity Coronaviruses COVID-19 Drug delivery Ferritin Fusion protein Glycoproteins N-Terminus Protein structure Proteins Severe acute respiratory syndrome coronavirus 2 Spike glycoprotein Vaccines |
title | Human H-ferritin presenting RBM of spike glycoprotein as potential vaccine of SARS-CoV-2 |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T14%3A46%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_COVID&rft_val_fmt=info:ofi/fmt:kev:mtx:book&rft.genre=document&rft.atitle=Human%20H-ferritin%20presenting%20RBM%20of%20spike%20glycoprotein%20as%20potential%20vaccine%20of%20SARS-CoV-2&rft.jtitle=bioRxiv&rft.au=Yao,%20Dehui&rft.date=2020-06-08&rft.eissn=2692-8205&rft_id=info:doi/10.1101/2020.05.25.115618&rft_dat=%3Cproquest_COVID%3E2410538752%3C/proquest_COVID%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-b1528-c43895f489404c3d6881d4e2c96753af77a24173bf155c220c89daa9a0ceb4e03%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2410538752&rft_id=info:pmid/&rfr_iscdi=true |