Driscoll J, Duan C, Zuo Y, Xu T, Troxler R, Oppenheim F G
Department of Periodontology and Oral Biology, School of Graduate Dentistry, Boston University Medical Center, MA 02118, USA.
Gene. 1996 Oct 24;177(1-2):29-34. doi: 10.1016/0378-1119(96)00265-x.
Histatin 5 (Hst5) is a 24-amino acid (aa) member of the Hst family that is found in human salivary secretions and exhibits candidacidal activity. Hst5 contains a 13-aa region that alone is capable of killing fungal pathogens and is referred to as the functional domain. To investigate the role of specific aa located within the functional domain, the pRSET bacterial expression system was used to produce recombinant Hst5 (re-Hst5) and several re-variants that were generated by site-directed mutagenesis. The vector pRSETC expresses genes of interest as fusion proteins attached to the carboxy end of an N-terminal His6 tag that binds to nickel (Ni2+). The re-variants were generated using the polymerase chain reaction (PCR) and had Gly substituted for either the His, Glu or Lys/Arg within the functional domain. PCR products that encoded either the wild-type or variant forms of re-Hst5 were inserted into pRSETC and produced as fusion proteins which were affinity purified from cell lysates by Ni(2+)-Sepharose chromatography. Fusion proteins were digested with CNBr and re-Hsts were purified by reversed-phase high performance liquid chromatography (RP-HPLC). Re-Hsts were tested in bioassays to measure the ability to kill both Candida albicans (C. albicans) blastoconidia and spheroplasts which were generated by removal of the cell wall. In both assays, re-Hst5 displayed dose-dependent candidacidal activity that was nearly identical to that of native Hst5 purified from human salivary secretions. Re-Hst5 variants with either Glu or Lys/Arg substitutions demonstrated significantly lower candidacidal activity in both assays, while the variant with His mutated showed essentially no activity at physiological concentrations. These results indicate that acidic and basic aa within the functional domain contribute to candidacidal activity and that the His are essential for candidacidal activity. Additionally, since C. albicans spheroplasts were also susceptible to Hsts, the cell wall is not an essential component in the Hst mechanism of candidacidal action.
组蛋白5(Hst5)是组蛋白家族的一个由24个氨基酸组成的成员,存在于人类唾液分泌物中,并具有杀念珠菌活性。Hst5包含一个13个氨基酸的区域,该区域本身就能够杀死真菌病原体,被称为功能域。为了研究功能域内特定氨基酸的作用,使用pRSET细菌表达系统产生重组Hst5(re-Hst5)和通过定点诱变产生的几种重组变体。载体pRSETC将感兴趣的基因表达为与N端His6标签的羧基末端相连的融合蛋白,该标签与镍(Ni2+)结合。使用聚合酶链反应(PCR)产生重组变体,并在功能域内将甘氨酸替换为His、Glu或Lys/Arg。编码re-Hst5野生型或变体形式的PCR产物被插入pRSETC,并作为融合蛋白产生,通过Ni(2+)-琼脂糖凝胶层析从细胞裂解物中进行亲和纯化。融合蛋白用溴化氰消化,re-Hsts通过反相高效液相色谱(RP-HPLC)纯化。在生物测定中测试re-Hsts杀死白色念珠菌(白色念珠菌)芽生孢子和通过去除细胞壁产生的原生质球的能力。在这两种测定中,re-Hst5均表现出剂量依赖性的杀念珠菌活性,这与从人类唾液分泌物中纯化的天然Hst5几乎相同。在这两种测定中,用Glu或Lys/Arg替代的re-Hst5变体表现出明显较低的杀念珠菌活性,而His突变的变体在生理浓度下基本没有活性。这些结果表明,功能域内的酸性和碱性氨基酸有助于杀念珠菌活性,而His对杀念珠菌活性至关重要。此外,由于白色念珠菌原生质球也易受Hsts影响,细胞壁不是Hst杀念珠菌作用机制中的必需成分。