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Testing an Electrostatic Interaction Hypothesis of Hepatitis B Virus Capsid Stability by Using an In Vitro Capsid Disassembly/Reassembly System

机译:通过使用体外衣壳拆卸/重组系统测试乙型肝炎病毒衣壳稳定性的静电相互作用假说

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摘要

To test a previously coined “charge balance hypothesis” of human hepatitis B virus (HBV) capsid stability, we established an in vitro disassembly and reassembly system using bacterially expressed HBV capsids. Capsid disassembly can be induced by micrococcal nuclease digestion of encapsidated RNA. HBV core protein (HBc) mutants containing various amounts of arginine were constructed by serial truncations at the C terminus. Capsids containing smaller amounts of arginine (HBc 149, 154, and 157) remained intact after micrococcal nuclease digestion by native gel electrophoresis. Capsids containing larger amounts of arginine (HBc 159, 164, 169, and 171) exhibited reduced and more diffuse banding intensity and slightly upshifted mobility (HBc 159 and 164). Capsids containing the largest amounts of arginine (HBc 173, 175, and 183), as well as HBc 167, exhibited no detectable banding signal, indicating loss of capsid integrity or stability. Interestingly, capsid reassembly can be induced by polyanions, including oligonucleotides, poly-glutamic acid, and nonbiological polymer (polyacrylic acid). In contrast, polycations (polylysine and polyethylenimine) and low-molecular-weight anions (inositol triphosphate) induced no capsid reassembly. Results obtained by gel assay were confirmed by electron microscopy. Reassembled capsids comigrated with undigested parental capsids on agarose gels and cosedimented with undigested capsids by sucrose gradient ultracentrifugation. Taken together, the results indicate that HBV capsid assembly and integrity depend on polyanions, which probably can help minimize intersubunit charge repulsion caused mainly by arginine-rich domain III or IV in close contact. The exact structure of polyanions is not important for in vitro capsid reassembly. A large amount of independent experimental evidence for this newly coined “electrostatic interaction hypothesis” is discussed.
机译:为了测试先前创造的人类乙型肝炎病毒(HBV)衣壳稳定性的“电荷平衡假说”,我们使用细菌表达的HBV衣壳建立了体外拆卸和重组系统。衣壳RNA的微球菌核酸酶消化可以诱导衣壳解体。通过在C末端进行连续截短构建了含有各种精氨酸的HBV核心蛋白(HBc)突变体。通过天然凝胶电泳消化微球菌核酸酶后,含有少量精氨酸(HBc 149、154和157)的衣壳保持完整。含有大量精氨酸(HBc 159、164、169和171)的衣壳显示出降低的条带强度和更大的扩散条带以及略微上移的迁移率(HBc 159和164)。含有最大量精氨酸(HBc 173、175和183)以及HBc 167的衣壳没有可检测到的条带信号,表明衣壳完整性或稳定性下降。有趣的是,衣壳重组可以由包括寡核苷酸,聚谷氨酸和非生物聚合物(聚丙烯酸)在内的聚阴离子诱导。相反,聚阳离子(聚赖氨酸和聚乙烯亚胺)和低分子量阴离子(三磷酸肌醇)不会引起衣壳重组。通过凝胶测定获得的结果通过电子显微镜确认。在琼脂糖凝胶上重新组装的衣壳与未消化的亲本衣壳一起发酵,并通过蔗糖梯度超速离心与未消化的衣壳进行共沉淀。两者合计,结果表明HBV衣壳的组装和完整性取决于聚阴离子,这可能有助于使主要由富含精氨酸的结构域III或IV紧密接触引起的亚基间电荷排斥最小化。聚阴离子的确切结构对于体外衣壳重组而言并不重要。讨论了有关这一新创造的“静电相互作用假设”的大量独立实验证据。

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