Jindadamrongwech S, Thepparit C, Smith D R
Molecular Pathology Laboratory, Institute of Molecular Biology and Genetics, Mahidol University, Nakorn Pathom, Thailand.
Arch Virol. 2004 May;149(5):915-27. doi: 10.1007/s00705-003-0263-x. Epub 2004 Jan 5.
This study sought to identify receptor elements for dengue virus serotype 2 on human liver cells (HepG2) using the viral overlay protein binding assay (VOPBA) technique and Mass Spectrometry fingerprinting. A single major and several minor virus binding bands were observed, and mass spectrometry identified a candidate binding protein for the major binding band as GRP 78 (BiP). GRP78 expression on the cell surface was confirmed, and antibodies directed against both the N and C-terminus of GRP 78 (BiP) altered both the binding of the virus to the cell surface as well as the infectivity profile of HepG2 cells in response to dengue serotype 2 infection. GRP 78 (BiP), which has previously been identified as a co-receptor protein for coxsackievirus A9, is the first non-Fc receptor protein identified for the dengue virus, although GRP78 probably functions as part of a receptor complex.
本研究旨在利用病毒覆盖蛋白结合分析(VOPBA)技术和质谱指纹图谱法,鉴定人类肝癌细胞(HepG2)上登革病毒2型的受体元件。观察到一条主要的病毒结合带和几条次要的病毒结合带,质谱分析确定主要结合带的候选结合蛋白为GRP 78(BiP)。证实了GRP78在细胞表面的表达,针对GRP 78(BiP)N端和C端的抗体改变了病毒与细胞表面的结合以及HepG2细胞对登革2型病毒感染的感染特性。GRP 78(BiP)先前已被鉴定为柯萨奇病毒A9的共受体蛋白,它是首个被鉴定出的登革病毒非Fc受体蛋白,尽管GRP78可能作为受体复合物的一部分发挥作用。