Yesilkaya Hasan, Soma-Haddrick Shital, Crennell Susan J, Andrew Peter W
Department of Infection, Immunity and Inflammation, Maurice Shock Building, University of Leicester, PO Box 138, Leicester, LE1 9HN, UK.
Res Microbiol. 2006 Jul-Aug;157(6):569-74. doi: 10.1016/j.resmic.2005.12.009. Epub 2006 Feb 13.
We characterised pneumococcal neuraminidase A (NanA) by determining key amino acids required for the enzymatic activity of the protein. Single replacement of two residues, hypothesised to be important for the catalytic activity of neuraminidases, resulted in total loss of activity (E647 with Q or Y752 with F). The mutation of R663 to H caused substantial reduction in the catalytic ability of the enzyme. The inactive neuraminidases thus produced were protective immunogens against pneumococcal pneumonia in mice.
我们通过确定该蛋白酶活性所需的关键氨基酸来对肺炎球菌神经氨酸酶A(NanA)进行表征。对两个据推测对神经氨酸酶催化活性很重要的残基进行单一位点替换,导致活性完全丧失(E647替换为Q或Y752替换为F)。R663突变为H导致该酶的催化能力大幅降低。由此产生的无活性神经氨酸酶是小鼠肺炎球菌肺炎的保护性免疫原。