ACE2-Decorated Virus-Like Particles Effectively Block SARS-CoV-2 Infection.


Journal

International journal of nanomedicine
ISSN: 1178-2013
Titre abrégé: Int J Nanomedicine
Pays: New Zealand
ID NLM: 101263847

Informations de publication

Date de publication:
2024
Historique:
received: 23 10 2023
accepted: 02 05 2024
medline: 15 7 2024
pubmed: 15 7 2024
entrez: 15 7 2024
Statut: epublish

Résumé

Over the past three years, extensive research has been dedicated to understanding and combating COVID-19. Targeting the interaction between the SARS-CoV-2 Spike protein and the ACE2 receptor has emerged as a promising therapeutic strategy against SARS-CoV-2. This study aimed to develop ACE2-coated virus-like particles (ACE2-VLPs), which can be utilized to prevent viral entry into host cells and efficiently neutralize the virus. Virus-like particles were generated through the utilization of a packaging plasmid in conjunction with a plasmid containing the ACE2 envelope sequence. Subsequently, ACE2-VLPs and ACE2-EVs were purified via ultracentrifugation. The quantification of VLPs was validated through multiple methods, including Nanosight 3000, TEM imaging, and Western blot analysis. Various packaging systems were explored to optimize the ACE2-VLP configuration for enhanced neutralization capabilities. The evaluation of neutralization effectiveness was conducted using pseudoviruses bearing different spike protein variants. Furthermore, the study assessed the neutralization potential against the Omicron BA.1 variant in Vero E6 cells. ACE2-VLPs showed a high neutralization capacity even at low doses and demonstrated superior efficacy in in vitro pseudoviral assays compared to extracellular vesicles carrying ACE2. ACE2-VLPs remained stable under various environmental temperatures and effectively blocked all tested variants of concern in vitro. Notably, they exhibited significant neutralization against Omicron BA.1 variant in Vero E6 cells. Given their superior efficacy compared to extracellular vesicles and proven success against live virus, ACE2-VLPs stand out as crucial candidates for treating SARS-CoV-2 infections. This novel therapeutic approach of coating VLPs with receptor particles provides a proof-of-concept for designing effective neutralization strategies for other viral diseases in the future.

Identifiants

pubmed: 39005960
doi: 10.2147/IJN.S446093
pii: 446093
pmc: PMC11246629
doi:

Substances chimiques

Angiotensin-Converting Enzyme 2 EC 3.4.17.23
Spike Glycoprotein, Coronavirus 0
ACE2 protein, human EC 3.4.17.23
spike protein, SARS-CoV-2 0
Antibodies, Neutralizing 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

6931-6943

Informations de copyright

© 2024 Bayraktar et al.

Déclaration de conflit d'intérêts

The authors declare no conflicts of interest in this work.

Auteurs

Canan Bayraktar (C)

Koç University Research Center for Translational Medicine (KUTTAM), Koç University, Istanbul, Turkey.

Alisan Kayabolen (A)

Koç University Research Center for Translational Medicine (KUTTAM), Koç University, Istanbul, Turkey.

Arda Odabas (A)

Koç University Research Center for Translational Medicine (KUTTAM), Koç University, Istanbul, Turkey.

Aysegul Durgun (A)

Koç University Research Center for Translational Medicine (KUTTAM), Koç University, Istanbul, Turkey.

Ipek Kok (I)

Koç University Research Center for Translational Medicine (KUTTAM), Koç University, Istanbul, Turkey.

Kenan Sevinc (K)

Koç University Research Center for Translational Medicine (KUTTAM), Koç University, Istanbul, Turkey.

Aroon Supramaniam (A)

Menzies Health Institute Queensland, School of Medical Science Griffith University, Gold Coast Campus, Brisbane, QLD, Australia.

Adi Idris (A)

Menzies Health Institute Queensland, School of Medical Science Griffith University, Gold Coast Campus, Brisbane, QLD, Australia.
Centre for Immunology and Infection Control, School of Biomedical Sciences, Queensland University of Technology, Brisbane, QLD, Australia.

Tugba Bagci-Onder (T)

Koç University Research Center for Translational Medicine (KUTTAM), Koç University, Istanbul, Turkey.

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Classifications MeSH