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Identification of a nanobody able to catalyze the destruction of the spike-trimer of SARS-CoV-2
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作者 Kai Wang Duanfang Cao +9 位作者 Lanlan Liu Xiaoyi Fan Yihuan Lin Wenting He Yunze Zhai Pingyong Xu Xiyun Yan Haikun Wang Xinzheng Zhang Pengyuan Yang 《Frontiers of Medicine》 2025年第3期493-506,共14页
Neutralizing antibodies have been designed to specifically target and bind to the receptor binding domain(RBD)of spike(S)protein to block severe acute respiratory syndrome coronavirus 2(SARS-CoV-2)virus from attaching... Neutralizing antibodies have been designed to specifically target and bind to the receptor binding domain(RBD)of spike(S)protein to block severe acute respiratory syndrome coronavirus 2(SARS-CoV-2)virus from attaching to angiotensin converting enzyme 2(ACE2).This study reports a distinctive nanobody,designated as VHH21,that directly catalyzes the S-trimer into an irreversible transition state through postfusion conformational changes.Derived from camels immunized with multiple antigens,a set of nanobodies with high affinity for the S1 protein displays abilities to neutralize pseudovirion infections with a broad resistance to variants of concern of SARS-CoV-2,including SARS-CoV and BatRaTG13.Importantly,a super-resolution screening and analysis platform based on visual fluorescence probes was designed and applied to monitor single proteins and protein subunits.A spontaneously occurring dimeric form of VHH21 was obtained to rapidly destroy the S-trimer.Structural analysis via cryogenic electron microscopy revealed that VHH21 targets specific conserved epitopes on the S protein,distinct from the ACE2 binding site on the RBD,which destabilizes the fusion process.This research highlights the potential of VHH21 as an abzyme-like nanobody(nanoabzyme)possessing broad-spectrum binding capabilities and highly effective anti-viral properties and offers a promising strategy for combating coronavirus outbreaks. 展开更多
关键词 NANOBODY SARS-CoV-2 spike-trimer catalyzation rapid destruction
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猫传染性腹膜炎病毒S蛋白纳米抗体的筛选与鉴定
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作者 储丽宇 薛希彤 +11 位作者 苗云博 唐国瑞 文晓晓 王学富 赵海鹏 侯江 芮萍 杨姗姗 王丽丽 李封赛 马增军 宋涛 《中国兽医杂志》 北大核心 2025年第10期25-32,共8页
为获取猫传染性腹膜炎病毒(FIPV)的特异性纳米抗体,本试验构建了表达FIPV重组三聚体刺突(RS)蛋白的真核质粒pCAGGS-FIPV-RS,利用人胚胎肾293悬浮细胞(HEK293F)表达并纯化FIPV RS蛋白;以纯化的FIPV RS蛋白作为包被抗原,利用噬菌体展示技... 为获取猫传染性腹膜炎病毒(FIPV)的特异性纳米抗体,本试验构建了表达FIPV重组三聚体刺突(RS)蛋白的真核质粒pCAGGS-FIPV-RS,利用人胚胎肾293悬浮细胞(HEK293F)表达并纯化FIPV RS蛋白;以纯化的FIPV RS蛋白作为包被抗原,利用噬菌体展示技术,从天然噬菌体展示文库中筛选出序列不同的纳米抗体基因;构建纳米抗体真核表达载体pCAGGS-VHH-Fc,利用人胚胎肾293贴壁细胞(HEK293T)进行试表达,通过蛋白免疫印记试验(Western blot)和间接酶联免疫吸附试验(ELISA)筛选能正常表达且具有高亲和力的纳米抗体,利用HEK293F细胞表达并纯化高亲和力的纳米抗体,通过间接免疫荧光试验(IFA)鉴定纯化后的纳米抗体与RS蛋白的反应原性。结果显示,本试验成功表达并纯化了FIPV RS蛋白;经过3轮噬菌体淘选后随机挑取41个阳性单克隆菌落,经测序分析,共筛选出10株序列不同的纳米抗体;成功构建pCAGGS-VHH-Fc重组真核表达质粒。Western blot和间接ELISA结果显示,其中7株纳米抗体与FIPV RS蛋白具有较好的反应原性;十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)证实了这7株纳米抗体在HEK293F细胞中成功大量表达和纯化;IFA结果显示,其中5株纳米抗体能够特异性结合FIPV RS蛋白。本试验可为FIPV的诊断、治疗和致病机理研究提供参考。 展开更多
关键词 猫传染性腹膜炎病毒(FIPV) 重组三聚体刺突(RS)蛋白 真核表达 噬菌体展示技术 纳米抗体
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