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寡聚结合物:生物工程可溶性淀粉样纳米颗粒,用于结合和中和 SARS-CoV-2。

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

机构信息

Institut de Biotecnologia i de Biomedicina (IBB) and Departament de Bioquímica i Biologia Molecular, Universitat Autònoma de Barcelona, Bellaterra, 08193 Barcelona, Spain.

Laboratory of Nanoscale Biology, Division of Biology and Chemistry, Paul Scherrer Institute, 5232 Villigen PSI, Switzerland.

出版信息

ACS Appl Mater Interfaces. 2023 Mar 8;15(9):11444-11457. doi: 10.1021/acsami.2c18305. Epub 2023 Feb 22.

Abstract

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 IC 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.

摘要

新型纳米颗粒可中和 SARS-CoV-2

由严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)感染引起的 2019 年冠状病毒病(COVID-19)大流行已成为主要的健康关注点。通过干扰 SARS-CoV-2 刺突(S)蛋白与人血管紧张素转换酶 2 受体(ACE2r)之间的相互作用来阻止病毒进入宿主细胞的分子为中和病毒开辟了一条有希望的途径。在这里,我们旨在创建一种新型的纳米颗粒,以中和 SARS-CoV-2。为此,我们利用模块化自组装策略来设计寡聚结合物,即通过两个先前描述的与 S 蛋白受体结合域(RBD)高亲和力结合的小型蛋白来修饰可溶性寡聚纳米颗粒。这些多价纳米结构与 RBD-ACE2r 相互作用竞争,并以皮摩尔范围的 IC 值中和 SARS-CoV-2 病毒样颗粒(SC2-VLPs),防止 SC2-VLPs 与表达 ACE2r 的细胞的膜融合。此外,寡聚结合物在血浆中具有生物相容性和显著稳定性。总之,我们描述了一种新型的基于蛋白质的纳米技术,它可能在 SARS-CoV-2 的治疗和诊断中得到应用。

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