Kurebayashi Yuuki
Jpn J Antibiot. 2016 Dec;69(6):357-366.
Influenza A and B viruses possess an enzyme "sialidase" that cleavages terminal sialic acid from glycochains. These viral sialidase proteins are highly expressed on the virus infected cells. We developed sialidase imaging probe "BTP3-Neu5Ac" that enables histochemical fluorescence staining of sialidase activity. BTP3-Neu5Ac was able to perform speedy and easy fluorescence imaging of these virus infected cells, with no needs of specific antibody and cell fixation. In addition, combination use of anti-influenza drugs (sialidase inhibitors) and BTP3-Neu5Ac resulted in selective fluorescence imaging for detection and high-efficiency isolation of drug-resistant virus. Fluorescence imaging of drug-resistant virus will be a powerful method for study of the drug-resistance mechanism, for monitoring of drug-resistant viruses. A novel tool for fluorescence imaging of viral sialidase activity is described in this review.
甲型和乙型流感病毒拥有一种能从糖链上切割末端唾液酸的酶“唾液酸酶”。这些病毒唾液酸酶蛋白在病毒感染的细胞上高度表达。我们开发了唾液酸酶成像探针“BTP3-Neu5Ac”,它能够对唾液酸酶活性进行组织化学荧光染色。BTP3-Neu5Ac能够对这些病毒感染的细胞进行快速且简便的荧光成像,无需特异性抗体和细胞固定。此外,抗流感药物(唾液酸酶抑制剂)与BTP3-Neu5Ac联合使用可实现选择性荧光成像,用于检测和高效分离耐药病毒。耐药病毒的荧光成像将成为研究耐药机制、监测耐药病毒的有力方法。本文综述了一种用于病毒唾液酸酶活性荧光成像的新型工具。