Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142, USA.
Department of Microbiology and Immunobiology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Nat Microbiol. 2016 Jun 20;1(8):16080. doi: 10.1038/nmicrobiol.2016.80.
Manipulation of proteins is key in assessing their in vivo function. Although genetic ablation is straightforward, reversible and specific perturbation of protein function remains a challenge. Single domain antibody fragments, such as camelid-derived VHHs, can serve as inhibitors or activators of intracellular protein function, but functional testing of identified VHHs is laborious. To address this challenge, we have developed a lentiviral screening approach to identify VHHs that elicit a phenotype when expressed intracellularly. We identified 19 antiviral VHHs that protect human A549 cells from lethal infection with influenza A virus (IAV) or vesicular stomatitis virus (VSV), respectively. Both negative-sense RNA viruses are vulnerable to VHHs uniquely specific for their respective nucleoproteins. Antiviral VHHs prevented nuclear import of viral ribonucleoproteins or mRNA transcription, respectively, and may provide clues for novel antiviral reagents. In principle, the screening approach described here should be applicable to identify inhibitors of any pathogen or biological pathway.
蛋白质的操作是评估其体内功能的关键。虽然基因敲除简单、直接且具有特异性,但对蛋白质功能的可逆性精确干扰仍然是一个挑战。单域抗体片段,如骆驼科来源的 VHH,可以作为细胞内蛋白功能的抑制剂或激活剂,但鉴定出的 VHH 的功能测试非常繁琐。为了解决这个问题,我们开发了一种慢病毒筛选方法,用于鉴定在细胞内表达时可引起表型的 VHH。我们鉴定出了 19 种抗流感病毒 A(IAV)或水疱性口炎病毒(VSV)的 VHH,它们分别保护人 A549 细胞免受致命感染。这两种负义 RNA 病毒都容易受到针对其各自核蛋白的独特特异性 VHH 的攻击。抗病毒 VHH 分别阻止了病毒核糖核蛋白的核内输入或 mRNA 转录,这可能为新型抗病毒试剂提供线索。原则上,本文描述的筛选方法应该适用于鉴定任何病原体或生物途径的抑制剂。