Feng Wenke, Cai Jian, Pierce William M, Song Zhao-Hui
Department of Pharmacology and Toxicology, University of Louisville School of Medicine, Louisville, KY 40292, USA.
Protein Expr Purif. 2002 Dec;26(3):496-505. doi: 10.1016/s1046-5928(02)00569-7.
To facilitate purification and structural characterization, the CB2 cannabinoid receptor is expressed in methylotrophic yeast Pichia pastoris. The expression plasmids were constructed in which the CB2 gene is under the control of the highly inducible promoter of P. pastoris alcohol oxidase 1 gene. A c-myc epitope and a hexahistidine tag were introduced at the C-terminal of the CB2 to permit easy detection and purification. In membrane preparations of CB2 gene transformed yeast cells, Western blot analysis detected the expression of CB2 proteins. Radioligand binding assays demonstrated that the CB2 receptors expressed in P. pastoris have a pharmacological profile similar to that of the receptors expressed in mammalian systems. Furthermore, the epitope-tagged receptor was purified by metal chelating chromatography and the purified CB2 preparations were subjected to digestion by trypsin. MALDI/TOF mass spectrometry analysis of the peptides extracted from tryptic digestions detected 14 peptide fragments derived from the CB2 receptor. ESI mass spectrometry was used to sequence one of these peptide fragments, thus, further confirming the identity of the purified receptor. In conclusion, these data demonstrated for the first time that epitope-tagged, functional CB2 cannabinoid receptor can be expressed in P. pastoris for purification.
为便于纯化和结构表征,CB2大麻素受体在甲基营养型酵母毕赤酵母中表达。构建了表达质粒,其中CB2基因受毕赤酵母醇氧化酶1基因的高度诱导型启动子控制。在CB2的C末端引入了一个c-myc表位和一个六组氨酸标签,以便于检测和纯化。在CB2基因转化酵母细胞的膜制剂中,蛋白质印迹分析检测到了CB2蛋白的表达。放射性配体结合试验表明,在毕赤酵母中表达的CB2受体具有与在哺乳动物系统中表达的受体相似的药理学特征。此外,通过金属螯合色谱法纯化了表位标记的受体,并将纯化的CB2制剂用胰蛋白酶消化。对胰蛋白酶消化产物中提取的肽段进行基质辅助激光解吸电离/飞行时间质谱分析,检测到14个源自CB2受体的肽段。用电喷雾质谱对其中一个肽段进行测序,从而进一步证实了纯化受体的身份。总之,这些数据首次证明,带有表位标签的功能性CB2大麻素受体可以在毕赤酵母中表达以进行纯化。