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通过荧光唾液酸酶成像检测和分离耐神经氨酸酶抑制剂流感病毒的高效方法。

High efficiency method of detection and isolation of neuraminidase inhibitor resistant influenza viruses by fluorescence sialidase imaging.

作者信息

Kurebayashi Yuuki

出版信息

Jpn J Antibiot. 2016 Dec;69(6):357-366.

Abstract

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.

摘要

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。

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