人基质金属蛋白酶2催化区的克隆与表达

为从随机肽库中寻找具有基质金属蛋白酶 2 (MMP 2 )抑制活性的新型小肽抑制剂 ,应用PCR法从含有人MMP 2基因的质粒中扩增了人MMP 2的催化区 .序列分析结果表明无氨基酸突变 .然后构建人MMP 2催化区的表达载体pET MCD ,转化大肠杆菌BL2 1(DE3 ) ,经IPTG诱导表达人MMP 2催化区 .经包涵体分离、变性、金属螯合层析纯化和复性等过程 ,复性后的人MMP 2催化区具有较好的明胶水解活性 .

Cloning and Expression of the Catalytic Domain of Human MMP-2

Matrix metalloproteinase 2(MMP\|2) is an important matrix metalloproteinase in the degradation of basement membranes and denatured collagens(gelatin),and is believed to play a key role in cancer invasion and metastasis.In order to screen inhibitors of MMP\|2,cDNA of the catalytic domain of MMP\|2 (MCD) was amplified by polymerase chain reaction(PCR) and was cloned into expression vector pET\|28c.The constructed expression vector was then transformed in \%E.coli\% BL21(DE3).SDS PAGE analysis indicated that MCD expressed in \%E.coli\% existed as inclusion bodies.The inclusion bodies were separated and dissolved in 8 mol/L urea.Then MCD was refolded in the presence of Zn2 and Ca 2 ,and purified by chelating affinity chromatography.Gelatin zymography analysis showed that the refolded MCD had an excellent gelatinolytic activity.