Hill J, Montgomery D S, Kay J
Department of Biochemistry, University of Wales College, Cardiff, UK.
FEBS Lett. 1993 Jul 12;326(1-3):101-4. doi: 10.1016/0014-5793(93)81770-z.
A cDNA for procathepsin E was generated from human gastric adenocarcinoma (AGS) cells, amplified by PCR and inserted into the T7 dependent vector pET 22b for expression in E. coli. Purification of the resultant product was accomplished simply, without the need to resort to column chromatography. The recombinant protein displayed comparable properties to those of its naturally occurring counterpart. The yield of homogeneous active enzyme obtained was approximately 3 mg per 40 g of cells. This is sufficient to permit crystallisation and structural analysis to begin and a mutagenesis programme to examine structure/activity relationships now to be undertaken.
从人胃腺癌细胞(AGS)中制备组织蛋白酶E原的互补DNA(cDNA),通过聚合酶链反应(PCR)进行扩增,并将其插入T7依赖载体pET 22b中,以便在大肠杆菌中表达。所得产物的纯化过程简单,无需采用柱色谱法。重组蛋白表现出与其天然对应物相当的特性。每40克细胞获得的同源活性酶产量约为3毫克。这足以开始进行结晶和结构分析,并开展一个诱变程序来研究结构/活性关系。