Multivalent 9-O-Acetylated-sialic acid glycoclusters as potent inhibitors for SARS-CoV-2 infection

The recent emergence of highly transmissible SARS-CoV-2 variants illustrates the urgent need to better understand the molecular details of the virus binding to its host cell and to develop anti-viral strategies. While many studies focused on the role of the angiotensin-converting enzyme 2 receptor i...

Full description

Saved in:
Bibliographic Details
Main Authors: Petitjean, Simon J. L. (Author) , Chen, Wenzhang (Author) , Koehler, Melanie (Author) , Jimmidi, Ravikumar (Author) , Yang, Jinsung (Author) , Mohammed, Danahe (Author) , Juniku, Blinera (Author) , Stanifer, Megan (Author) , Boulant, Steeve (Author) , Vincent, Stéphane P. (Author) , Alsteens, David (Author)
Format: Article (Journal)
Language:English
Published: 10 May 2022
In: Nature Communications
Year: 2022, Volume: 13, Pages: 1-12
ISSN:2041-1723
DOI:10.1038/s41467-022-30313-8
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1038/s41467-022-30313-8
Verlag, lizenzpflichtig, Volltext: https://www.nature.com/articles/s41467-022-30313-8
Get full text
Author Notes:Simon J.L. Petitjean, Wenzhang Chen, Melanie Koehler, Ravikumar Jimmidi, Jinsung Yang, Danahe Mohammed, Blinera Juniku, Megan L. Stanifer, Steeve Boulant, Stéphane P. Vincent & David Alsteens

MARC

LEADER 00000caa a2200000 c 4500
001 1807839095
003 DE-627
005 20230426062337.0
007 cr uuu---uuuuu
008 220627s2022 xx |||||o 00| ||eng c
024 7 |a 10.1038/s41467-022-30313-8  |2 doi 
035 |a (DE-627)1807839095 
035 |a (DE-599)KXP1807839095 
035 |a (OCoLC)1341461494 
040 |a DE-627  |b ger  |c DE-627  |e rda 
041 |a eng 
084 |a 33  |2 sdnb 
100 1 |a Petitjean, Simon J. L.  |e VerfasserIn  |0 (DE-588)126099810X  |0 (DE-627)1807840166  |4 aut 
245 1 0 |a Multivalent 9-O-Acetylated-sialic acid glycoclusters as potent inhibitors for SARS-CoV-2 infection  |c Simon J.L. Petitjean, Wenzhang Chen, Melanie Koehler, Ravikumar Jimmidi, Jinsung Yang, Danahe Mohammed, Blinera Juniku, Megan L. Stanifer, Steeve Boulant, Stéphane P. Vincent & David Alsteens 
264 1 |c 10 May 2022 
300 |a 12 
336 |a Text  |b txt  |2 rdacontent 
337 |a Computermedien  |b c  |2 rdamedia 
338 |a Online-Ressource  |b cr  |2 rdacarrier 
500 |a Gesehen am 27.06.2022 
520 |a The recent emergence of highly transmissible SARS-CoV-2 variants illustrates the urgent need to better understand the molecular details of the virus binding to its host cell and to develop anti-viral strategies. While many studies focused on the role of the angiotensin-converting enzyme 2 receptor in the infection, others suggest the important role of cell attachment factors such as glycans. Here, we use atomic force microscopy to study these early binding events with the focus on the role of sialic acids (SA). We show that SARS-CoV-2 binds specifically to 9-O-acetylated-SA with a moderate affinity, supporting its role as an attachment factor during virus landing to cell host surfaces. For therapeutic purposes and based on this finding, we have designed novel blocking molecules with various topologies and carrying a controlled number of SA residues, enhancing affinity through a multivalent effect. Inhibition assays show that the AcSA-derived glycoclusters are potent inhibitors of cell binding and infectivity, offering new perspectives in the treatment of SARS-CoV-2 infection. 
650 4 |a Applications of AFM 
650 4 |a Nanoscale biophysics 
650 4 |a SARS-CoV-2 
700 1 |a Chen, Wenzhang  |e VerfasserIn  |4 aut 
700 1 |a Koehler, Melanie  |e VerfasserIn  |4 aut 
700 1 |a Jimmidi, Ravikumar  |e VerfasserIn  |4 aut 
700 1 |a Yang, Jinsung  |e VerfasserIn  |4 aut 
700 1 |a Mohammed, Danahe  |e VerfasserIn  |4 aut 
700 1 |a Juniku, Blinera  |e VerfasserIn  |4 aut 
700 1 |a Stanifer, Megan  |e VerfasserIn  |0 (DE-588)1130687643  |0 (DE-627)884888835  |0 (DE-576)486922367  |4 aut 
700 1 |a Boulant, Steeve  |e VerfasserIn  |0 (DE-588)1130687430  |0 (DE-627)884888509  |0 (DE-576)48692243X  |4 aut 
700 1 |a Vincent, Stéphane P.  |e VerfasserIn  |4 aut 
700 1 |a Alsteens, David  |e VerfasserIn  |4 aut 
773 0 8 |i Enthalten in  |t Nature Communications  |d [London] : Springer Nature, 2010  |g 13(2022), Artikel-ID 2564, Seite 1-12  |h Online-Ressource  |w (DE-627)626457688  |w (DE-600)2553671-0  |w (DE-576)331555905  |x 2041-1723  |7 nnas  |a Multivalent 9-O-Acetylated-sialic acid glycoclusters as potent inhibitors for SARS-CoV-2 infection 
773 1 8 |g volume:13  |g year:2022  |g elocationid:2564  |g pages:1-12  |g extent:12  |a Multivalent 9-O-Acetylated-sialic acid glycoclusters as potent inhibitors for SARS-CoV-2 infection 
856 4 0 |u https://doi.org/10.1038/s41467-022-30313-8  |x Verlag  |x Resolving-System  |z lizenzpflichtig  |3 Volltext 
856 4 0 |u https://www.nature.com/articles/s41467-022-30313-8  |x Verlag  |z lizenzpflichtig  |3 Volltext 
951 |a AR 
992 |a 20220627 
993 |a Article 
994 |a 2022 
998 |g 1130687430  |a Boulant, Steeve  |m 1130687430:Boulant, Steeve  |d 50000  |e 50000PB1130687430  |k 0/50000/  |p 9 
998 |g 1130687643  |a Stanifer, Megan  |m 1130687643:Stanifer, Megan  |d 50000  |e 50000PS1130687643  |k 0/50000/  |p 8 
999 |a KXP-PPN1807839095  |e 4156717429 
BIB |a Y 
SER |a journal 
JSO |a {"title":[{"title":"Multivalent 9-O-Acetylated-sialic acid glycoclusters as potent inhibitors for SARS-CoV-2 infection","title_sort":"Multivalent 9-O-Acetylated-sialic acid glycoclusters as potent inhibitors for SARS-CoV-2 infection"}],"language":["eng"],"person":[{"role":"aut","given":"Simon J. L.","display":"Petitjean, Simon J. L.","family":"Petitjean"},{"role":"aut","given":"Wenzhang","display":"Chen, Wenzhang","family":"Chen"},{"display":"Koehler, Melanie","role":"aut","given":"Melanie","family":"Koehler"},{"display":"Jimmidi, Ravikumar","given":"Ravikumar","role":"aut","family":"Jimmidi"},{"family":"Yang","display":"Yang, Jinsung","role":"aut","given":"Jinsung"},{"display":"Mohammed, Danahe","given":"Danahe","role":"aut","family":"Mohammed"},{"family":"Juniku","given":"Blinera","role":"aut","display":"Juniku, Blinera"},{"family":"Stanifer","display":"Stanifer, Megan","role":"aut","given":"Megan"},{"family":"Boulant","display":"Boulant, Steeve","role":"aut","given":"Steeve"},{"family":"Vincent","role":"aut","given":"Stéphane P.","display":"Vincent, Stéphane P."},{"family":"Alsteens","display":"Alsteens, David","given":"David","role":"aut"}],"name":{"displayForm":["Simon J.L. Petitjean, Wenzhang Chen, Melanie Koehler, Ravikumar Jimmidi, Jinsung Yang, Danahe Mohammed, Blinera Juniku, Megan L. Stanifer, Steeve Boulant, Stéphane P. Vincent & David Alsteens"]},"id":{"eki":["1807839095"],"doi":["10.1038/s41467-022-30313-8"]},"physDesc":[{"extent":"12 S."}],"note":["Gesehen am 27.06.2022"],"relHost":[{"note":["Gesehen am 13.06.24"],"physDesc":[{"extent":"Online-Ressource"}],"id":{"zdb":["2553671-0"],"issn":["2041-1723"],"eki":["626457688"]},"disp":"Multivalent 9-O-Acetylated-sialic acid glycoclusters as potent inhibitors for SARS-CoV-2 infectionNature Communications","origin":[{"publisher":"Springer Nature ; Nature Publishing Group UK","dateIssuedDisp":"[2010]-","publisherPlace":"[London] ; [London]"}],"recId":"626457688","type":{"bibl":"periodical","media":"Online-Ressource"},"pubHistory":["2010-"],"language":["eng"],"part":{"text":"13(2022), Artikel-ID 2564, Seite 1-12","year":"2022","volume":"13","extent":"12","pages":"1-12"},"title":[{"title_sort":"Nature Communications","title":"Nature Communications"}]}],"type":{"bibl":"article-journal","media":"Online-Ressource"},"origin":[{"dateIssuedKey":"2022","dateIssuedDisp":"10 May 2022"}],"recId":"1807839095"} 
SRT |a PETITJEANSMULTIVALEN1020