OligoBinders: Bioengineered Soluble Amyloid-like Nanoparticles to Bind and Neutralize SARS-CoV-2

被引:4
作者
Behbahanipour, Molood [1 ,2 ]
Benoit, Roger [3 ]
Navarro, Susanna [1 ,2 ]
Ventura, Salvador [1 ,2 ]
机构
[1] Univ Autonoma Barcelona, Inst Biotecnol & Biomed IBB, Barcelona 08193, Spain
[2] Univ Autonoma Barcelona, Dept Bioquim & Biol Mol, Barcelona 08193, Spain
[3] Paul Scherrer Inst, Div Biol & Chem, Lab Nanoscale Biol, CH-5232 Villigen, Switzerland
关键词
SARS-CoV-2; spike protein; coronavirus; nanoparticles; soluble oligomers; protein assemblies; virus inactivation; antiviral agents;
D O I
10.1021/acsami.2c18305
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has become a primary health concern. Molecules that prevent viral entry into host cells by interfering with the interaction between SARS-CoV-2 spike (S) protein and the human angiotensin-converting enzyme 2 receptor (ACE2r) opened a promising avenue for virus neutralization. Here, we aimed to create a novel kind of nanoparticle that can neutralize SARS-CoV-2. To this purpose, we exploited a modular self-assembly strategy to engineer OligoBinders, soluble oligomeric nanoparticles decorated with two miniproteins previously described to bind to the S protein receptor binding domain (RBD) with high affinity. The multivalent nanostructures compete with the RBD-ACE2r interaction and neutralize SARS-CoV-2 virus-like particles (SC2-VLPs) with IC50 values in the pM range, preventing SC2-VLPs fusion with the membrane of ACE2r-expressing cells. Moreover, OligoBinders are biocompatible and significantly stable in plasma. Overall, we describe a novel protein-based nanotechnology that might find application in SARS-CoV-2 therapeutics and diagnostics.
引用
收藏
页码:11444 / 11457
页数:14
相关论文
共 57 条
[1]   Intraarticular triamcinolone hexacetonide, stanozolol, Hylan G-F 20 and platelet concentrate in a naturally occurring canine osteoarthritis model [J].
Alves, J. C. ;
Santos, A. ;
Jorge, P. ;
Lavrador, C. ;
Miguel Carreira, L. .
SCIENTIFIC REPORTS, 2021, 11 (01)
[2]   Remdesivir for the treatment of COVID-19 [J].
Ansems, Kelly ;
Grundeis, Felicitas ;
Dahms, Karolina ;
Mikolajewska, Agata ;
Thieme, Volker ;
Piechotta, Vanessa ;
Metzendorf, Maria-Inti ;
Stegemann, Miriam ;
Benstoem, Carina ;
Fichtner, Falk .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2021, (08)
[3]   Amyloidogenicity as a driving force for the formation of functional oligomers [J].
Azizyan, Rafayel A. ;
Wang, Weiqiang ;
Anikeenko, Alexey ;
Radkova, Zinaida ;
Bakulina, Anastasia ;
Garro, Adriana ;
Charlier, Landry ;
Dumas, Christian ;
Ventura, Salvador ;
Kajava, Andrey, V .
JOURNAL OF STRUCTURAL BIOLOGY, 2020, 212 (01)
[4]   Establishment of Constraints on Amyloid Formation Imposed by Steric Exclusion of Globular Domains [J].
Azizyan, Rafayel A. ;
Garro, Adriana ;
Radkova, Zinaida ;
Anikeenko, Alexey ;
Bakulina, Anastasia ;
Dumas, Christian ;
Kajava, Andrey V. .
JOURNAL OF MOLECULAR BIOLOGY, 2018, 430 (20) :3835-3846
[5]   Characterization of Soft Amyloid Cores in Human Prion-Like Proteins [J].
Batlle, Cristina ;
Sanchez de Groot, Natalia ;
Iglesias, Valentin ;
Navarro, Susanna ;
Ventura, Salvador .
SCIENTIFIC REPORTS, 2017, 7
[6]   Design, Expression, Purification, and Characterization of a YFP-Tagged 2019-nCoV Spike Receptor-Binding Domain Construct [J].
Bierig, Tobias ;
Collu, Gabriella ;
Blanc, Alain ;
Poghosyan, Emiliya ;
Benoit, Roger M. .
FRONTIERS IN BIOENGINEERING AND BIOTECHNOLOGY, 2020, 8
[7]   Stability matters, too - the thermodynamics of amyloid fibril formation [J].
Buell, Alexander K. .
CHEMICAL SCIENCE, 2022, 13 (35) :10177-10192
[8]   A Multifunctional Neutralizing Antibody-Conjugated Nanoparticle Inhibits and Inactivates SARS-CoV-2 [J].
Cai, Xiaolei ;
Chen, Min ;
Prominski, Aleksander ;
Lin, Yiliang ;
Ankenbruck, Nicholas ;
Rosenberg, Jillian ;
Nguyen, Mindy ;
Shi, Jiuyun ;
Tomatsidou, Anastasia ;
Randall, Glenn ;
Missiakas, Dominique ;
Fung, John ;
Chang, Eugene B. ;
Penaloza-MacMaster, Pablo ;
Tian, Bozhi ;
Huang, Jun .
ADVANCED SCIENCE, 2022, 9 (02)
[9]   De novo design of picomolar SARS-CoV-2 miniprotein inhibitors [J].
Cao, Longxing ;
Goreshnik, Inna ;
Coventry, Brian ;
Case, James Brett ;
Miller, Lauren ;
Kozodoy, Lisa ;
Chen, Rita E. ;
Carter, Lauren ;
Walls, Alexandra C. ;
Park, Young-Jun ;
Strauch, Eva-Maria ;
Stewart, Lance ;
Diamond, Michael S. ;
Veesler, David ;
Baker, David .
SCIENCE, 2020, 370 (6515) :426-+
[10]   Structural characterization of toxic oligomers that are kinetically trapped during α-synuclein fibril formation [J].
Chen, Serene W. ;
Drakulic, Srdja ;
Deas, Emma ;
Ouberai, Myriam ;
Aprile, Francesco A. ;
Arranz, Rocio ;
Ness, Samuel ;
Roodveldt, Cintia ;
Guilliams, Tim ;
De-Genst, Erwin J. ;
Klenerman, David ;
Wood, Nicholas W. ;
Knowles, Tuomas P. J. ;
Alfonso, Carlos ;
Rivas, German ;
Abramov, Andrey Y. ;
Maria Valpuesta, Jose ;
Dobson, Christopher M. ;
Cremades, Nunilo .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2015, 112 (16) :E1994-E2003