人同型融合和蛋白质分选复合体亚基的原核表达、蛋白纯化及功能验证

Prokaryotic expression, protein purification and functional verification of human homotypic fusion and vacuole protein sorting complex subunit

摘要:

同型融合和蛋白质分选复合体 (HOPS) 由VPS11、VPS16、VPS18、VPS33、VPS39和VPS41这6种蛋白组成，能够通过膜融合机制来调节生物体内的膜泡运输。已有研究表明其可以作为融合因子来促进自噬体与溶酶体膜融合过程。为在体外确定HOPS复合体与自噬性SNARE蛋白STX17是否具有直接相互作用，首先利用PCR技术从已有质粒中扩增得到6种基因的编码序列，将其连接至pGEX 4T-1-GST或pET-His-NusA原核表达载体上，经菌落PCR初步鉴定和DNA测序无误后成功构建6种原核表达重组质粒并转化至大肠杆菌BL21(DE3)；利用谷胱甘肽琼脂糖树脂与镍柱对重组蛋白进行纯化，烟草蚀纹病毒 (TEV) 蛋白酶酶切掉GST或His-NusA标签，得到分子量约为105 kDa的HA-VPS11蛋白、97 kDa的Flag-VPS16蛋白、108 kDa的HA-VPS18蛋白、70 kDa的Flag-VPS33蛋白、97 kDa的HA-VPS39蛋白和98 kDa的Flag-VPS41蛋白；通过体外GST pull-down技术对6种蛋白的功能进行验证，证实自噬性SNARE蛋白STX17和6种重组蛋白在体外均具有直接相互作用，为深入探究HOPS复合体参与自噬体与溶酶体膜融合过程中的功能及作用机制奠定实验基础。

Abstract:

Homotypic fusion and vacuole protein sorting(HOPS) is a protein complex consisting of VPS11, VPS16, VPS18, VPS33, VPS39, VPS41 and regulates membrane transport in vivo through membrane fusion mechanisms. The evidence suggests that HOPS complex as a fusion factor, facilitates autophagosome-lysosome fusion. To determine whether the HOPS complex directly interacts with the autophagic SNARE protein STX17 in vitro, the coding sequence of the six genes were amplified from the existing plasmids by PCR, and then ligated to the prokaryotic expression vector pGEX 4T-1-GST or pET-His-NusA. After identification through colony PCR and DNA sequencing, 6 recombinant plasmids were constructed and transferred into Escherichia coli BL21 (DE3). The recombinant proteins were purified by glutathione sepharose 4B and nickel column. We used the tobacco etch virus protease to cut off the GST-tag or His-NusA-tag, to obtain HA-VPS11 protein of about 105 kDa, Flag-VPS16 protein of about 97 kDa, HA-VPS18 protein of about 108 kDa, Flag-VPS33 protein of about 70?kDa, HA-VPS39 protein of about 97 kDa, and Flag-VPS41 protein of about 98 kDa. The function of the purified proteins was verified by in vitro glutathione S-transferases pull-down assay, confirming that autophagic SNARE protein STX17 interacted directly with HOPS components. Our findings provide experimental basis to further study the function and mechanism of HOPS complex in the process of autophagosome-lysosome fusion.