The Key Laboratory of Developmental Genes and Human Disease, Ministry of Education, Institute of Life Sciences, Southeast University, Nanjing 210096, People's Republic of China ; Jiangsu Nanobody Engineering and Research Center, Nantong 226010, People's Republic of China.
State Key Laboratory of Materials-Oriented Chemical Engineering, College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing 210009, People's Republic of China.
Nanoscale Res Lett. 2014 Sep 26;9(1):528. doi: 10.1186/1556-276X-9-528. eCollection 2014.
Our objective is to develop a rapid and sensitive assay based on magnetic beads to detect the concentration of influenza H3N2. The possibility of using variable domain heavy-chain antibodies (nanobody) as diagnostic tools for influenza H3N2 was investigated. A healthy camel was immunized with inactivated influenza H3N2. A nanobody library of 8 × 10(8) clones was constructed and phage displayed. After three successive biopanning steps, H3N2-specific nanobodies were successfully isolated, expressed in Escherichia coli, and purified. Sequence analysis of the nanobodies revealed that we possessed four classes of nanobodies against H3N2. Two nanobodies were further used to prepare our rapid diagnostic kit. Biotinylated nanobody was effectively immobilized onto the surface of streptavidin magnetic beads. The modified magnetic beads with nanobody capture specifically influenza H3N2 and can still be recognized by nanobodies conjugated to horseradish peroxidase (HRP) conjugates. Under optimized conditions, the present immunoassay exhibited a relatively high sensitive detection with a limit of 50 ng/mL. In conclusion, by combining magnetic beads with specific nanobodies, this assay provides a promising influenza detection assay to develop a potential rapid, sensitive, and low-cost diagnostic tool to screen for influenza infections.
我们的目标是开发一种基于磁珠的快速、灵敏的检测方法,以检测 H3N2 流感的浓度。本研究探讨了可变域重链抗体(纳米抗体)作为 H3N2 流感诊断工具的可能性。用灭活的 H3N2 流感对健康骆驼进行免疫。构建了 8×10(8)个克隆的纳米抗体文库,并进行了噬菌体展示。经过三轮生物淘选,成功分离出 H3N2 特异性纳米抗体,在大肠杆菌中表达并纯化。纳米抗体序列分析表明,我们拥有针对 H3N2 的四类纳米抗体。进一步用两种纳米抗体来制备我们的快速诊断试剂盒。生物素化纳米抗体有效地固定在链霉亲和素磁珠上。经纳米抗体修饰的磁珠特异性捕获 H3N2,并且仍然可以被辣根过氧化物酶(HRP)缀合物结合的纳米抗体识别。在优化的条件下,该免疫分析具有相对较高的灵敏性检测限为 50ng/mL。总之,通过将磁珠与特异性纳米抗体相结合,本研究提供了一种有前景的流感检测方法,有望开发出一种快速、灵敏、低成本的诊断工具来筛查流感感染。