Cargando…
Evaluation of SARS-CoV-2-Neutralizing Nanobody Using Virus Receptor Binding Domain-Administered Model Mice
Due to the rapid spread of coronavirus disease 2019 (COVID-19), there is an urgent requirement for the development of additional diagnostic tools for further analysis of the disease. The isolated nanobody Nb11-59 binds to the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) receptor-bind...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AAAS
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9343077/ https://www.ncbi.nlm.nih.gov/pubmed/35958110 http://dx.doi.org/10.34133/2022/9864089 |
_version_ | 1784760945827905536 |
---|---|
author | Liu, Song Li, Guanghui Ding, Lei Ding, Jin Zhang, Qian Li, Dan Hou, Xingguo Kong, Xiangxing Zou, Jing Zhang, Shiming Han, Hongbin Wan, Yakun Yang, Zhi Zhu, Hua |
author_facet | Liu, Song Li, Guanghui Ding, Lei Ding, Jin Zhang, Qian Li, Dan Hou, Xingguo Kong, Xiangxing Zou, Jing Zhang, Shiming Han, Hongbin Wan, Yakun Yang, Zhi Zhu, Hua |
author_sort | Liu, Song |
collection | PubMed |
description | Due to the rapid spread of coronavirus disease 2019 (COVID-19), there is an urgent requirement for the development of additional diagnostic tools for further analysis of the disease. The isolated nanobody Nb11-59 binds to the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) receptor-binding domain (RBD) with high affinity to neutralize the virus and block the angiotensin-converting enzyme 2- (ACE2-) RBD interaction. Here, we introduce a novel nanobody-based radiotracer named (68)Ga-Nb1159. The radiotracer retained high affinity for the RBD and showed reliable radiochemical characteristics both in vitro and in vivo. Preclinical positron emission tomography (PET) studies of (68)Ga-Nb1159 in mice revealed its rapid clearance from circulation and robust uptake into the renal and urinary systems. Fortunately, (68)Ga-Nb1159 could specifically reveal the distribution of the RBD in mice. This study also helped to evaluate the pharmacodynamic effects of the neutralizing nanobody. Moreover, (68)Ga-Nb1159 may be a promising tool to explore the distribution of the RBD and improve the understanding of the virus. In particular, this study identified a novel molecular radioagent and established a reliable evaluation method for specifically investigating the RBD through noninvasive and visual PET technology. |
format | Online Article Text |
id | pubmed-9343077 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | AAAS |
record_format | MEDLINE/PubMed |
spelling | pubmed-93430772022-08-10 Evaluation of SARS-CoV-2-Neutralizing Nanobody Using Virus Receptor Binding Domain-Administered Model Mice Liu, Song Li, Guanghui Ding, Lei Ding, Jin Zhang, Qian Li, Dan Hou, Xingguo Kong, Xiangxing Zou, Jing Zhang, Shiming Han, Hongbin Wan, Yakun Yang, Zhi Zhu, Hua Research (Wash D C) Research Article Due to the rapid spread of coronavirus disease 2019 (COVID-19), there is an urgent requirement for the development of additional diagnostic tools for further analysis of the disease. The isolated nanobody Nb11-59 binds to the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) receptor-binding domain (RBD) with high affinity to neutralize the virus and block the angiotensin-converting enzyme 2- (ACE2-) RBD interaction. Here, we introduce a novel nanobody-based radiotracer named (68)Ga-Nb1159. The radiotracer retained high affinity for the RBD and showed reliable radiochemical characteristics both in vitro and in vivo. Preclinical positron emission tomography (PET) studies of (68)Ga-Nb1159 in mice revealed its rapid clearance from circulation and robust uptake into the renal and urinary systems. Fortunately, (68)Ga-Nb1159 could specifically reveal the distribution of the RBD in mice. This study also helped to evaluate the pharmacodynamic effects of the neutralizing nanobody. Moreover, (68)Ga-Nb1159 may be a promising tool to explore the distribution of the RBD and improve the understanding of the virus. In particular, this study identified a novel molecular radioagent and established a reliable evaluation method for specifically investigating the RBD through noninvasive and visual PET technology. AAAS 2022-07-22 /pmc/articles/PMC9343077/ /pubmed/35958110 http://dx.doi.org/10.34133/2022/9864089 Text en Copyright © 2022 Song Liu et al. https://creativecommons.org/licenses/by/4.0/Exclusive Licensee Science and Technology Review Publishing House. Distributed under a Creative Commons Attribution License (CC BY 4.0). |
spellingShingle | Research Article Liu, Song Li, Guanghui Ding, Lei Ding, Jin Zhang, Qian Li, Dan Hou, Xingguo Kong, Xiangxing Zou, Jing Zhang, Shiming Han, Hongbin Wan, Yakun Yang, Zhi Zhu, Hua Evaluation of SARS-CoV-2-Neutralizing Nanobody Using Virus Receptor Binding Domain-Administered Model Mice |
title | Evaluation of SARS-CoV-2-Neutralizing Nanobody Using Virus Receptor Binding Domain-Administered Model Mice |
title_full | Evaluation of SARS-CoV-2-Neutralizing Nanobody Using Virus Receptor Binding Domain-Administered Model Mice |
title_fullStr | Evaluation of SARS-CoV-2-Neutralizing Nanobody Using Virus Receptor Binding Domain-Administered Model Mice |
title_full_unstemmed | Evaluation of SARS-CoV-2-Neutralizing Nanobody Using Virus Receptor Binding Domain-Administered Model Mice |
title_short | Evaluation of SARS-CoV-2-Neutralizing Nanobody Using Virus Receptor Binding Domain-Administered Model Mice |
title_sort | evaluation of sars-cov-2-neutralizing nanobody using virus receptor binding domain-administered model mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9343077/ https://www.ncbi.nlm.nih.gov/pubmed/35958110 http://dx.doi.org/10.34133/2022/9864089 |
work_keys_str_mv | AT liusong evaluationofsarscov2neutralizingnanobodyusingvirusreceptorbindingdomainadministeredmodelmice AT liguanghui evaluationofsarscov2neutralizingnanobodyusingvirusreceptorbindingdomainadministeredmodelmice AT dinglei evaluationofsarscov2neutralizingnanobodyusingvirusreceptorbindingdomainadministeredmodelmice AT dingjin evaluationofsarscov2neutralizingnanobodyusingvirusreceptorbindingdomainadministeredmodelmice AT zhangqian evaluationofsarscov2neutralizingnanobodyusingvirusreceptorbindingdomainadministeredmodelmice AT lidan evaluationofsarscov2neutralizingnanobodyusingvirusreceptorbindingdomainadministeredmodelmice AT houxingguo evaluationofsarscov2neutralizingnanobodyusingvirusreceptorbindingdomainadministeredmodelmice AT kongxiangxing evaluationofsarscov2neutralizingnanobodyusingvirusreceptorbindingdomainadministeredmodelmice AT zoujing evaluationofsarscov2neutralizingnanobodyusingvirusreceptorbindingdomainadministeredmodelmice AT zhangshiming evaluationofsarscov2neutralizingnanobodyusingvirusreceptorbindingdomainadministeredmodelmice AT hanhongbin evaluationofsarscov2neutralizingnanobodyusingvirusreceptorbindingdomainadministeredmodelmice AT wanyakun evaluationofsarscov2neutralizingnanobodyusingvirusreceptorbindingdomainadministeredmodelmice AT yangzhi evaluationofsarscov2neutralizingnanobodyusingvirusreceptorbindingdomainadministeredmodelmice AT zhuhua evaluationofsarscov2neutralizingnanobodyusingvirusreceptorbindingdomainadministeredmodelmice |