Department of Biomedical Sciences, Quillen College of Medicine, East Tennessee State University, Johnson City, Tennessee 37614, USA.
J Biol Chem. 2012 Dec 14;287(51):43116-25. doi: 10.1074/jbc.M112.427310. Epub 2012 Nov 8.
Human C-reactive protein (CRP) protects mice from lethal Streptococcus pneumoniae infection when injected into mice within the range of 6 h before to 2 h after the administration of pneumococci. Because CRP binds to phosphocholine-containing substances and subsequently activates the complement system, it has been proposed that the antipneumococcal function of CRP requires the binding of CRP to phosphocholine moieties present in pneumococcal cell wall C-polysaccharide. To test this proposal experimentally, in this study, we utilized a new CRP mutant incapable of binding to phosphocholine. Based on the structure of CRP-phosphocholine complexes, which showed that Phe(66), Thr(76), and Glu(81) formed the phosphocholine-binding pocket, we constructed a CRP mutant F66A/T76Y/E81A in which the pocket was blocked by substituting Tyr for Thr(76). When compared with wild-type CRP, mutant CRP bound more avidly to phosphoethanolamine and could be purified by affinity chromatography using phosphoethanolamine-conjugated Sepharose. Mutant CRP did not bind to phosphocholine, C-polysaccharide, or pneumococci. Mutant CRP was free in the mouse serum, and its rate of clearance in vivo was not faster than that of wild-type CRP. When either 25 μg or 150 μg of CRP was administered into mice, unlike wild-type CRP, mutant CRP did not protect mice from lethal pneumococcal infection. Mice injected with mutant CRP had higher mortality rates than mice that received wild-type CRP. Decreased survival was due to the increased bacteremia in mice treated with mutant CRP. We conclude that the phosphocholine-binding pocket on CRP is necessary for CRP-mediated initial protection of mice against lethal pneumococcal infection.
人 C-反应蛋白 (CRP) 在肺炎球菌给药前 6 小时至给药后 2 小时内注射入小鼠体内时可保护小鼠免受致死性肺炎球菌感染。因为 CRP 与含有磷酸胆碱的物质结合,随后激活补体系统,所以有人提出 CRP 的抗肺炎球菌功能需要 CRP 与肺炎球菌细胞壁 C-多糖中存在的磷酸胆碱部分结合。为了在实验上验证这一假说,在本研究中,我们利用了一种不能与磷酸胆碱结合的新型 CRP 突变体。基于 CRP-磷酸胆碱复合物的结构,其中显示 Phe(66)、Thr(76)和 Glu(81)形成了磷酸胆碱结合口袋,我们构建了一个 CRP 突变体 F66A/T76Y/E81A,其中口袋被 Tyr 取代 Thr(76)而被封闭。与野生型 CRP 相比,突变型 CRP 与磷酸乙醇胺结合更紧密,并可通过用磷酸乙醇胺偶联的 Sepharose 进行亲和层析进行纯化。突变型 CRP 不与磷酸胆碱、C-多糖或肺炎球菌结合。突变型 CRP 在小鼠血清中呈游离状态,其体内清除率并不比野生型 CRP 更快。当给予 25 μg 或 150 μg CRP 时,与野生型 CRP 不同,突变型 CRP 不能保护小鼠免受致死性肺炎球菌感染。用突变型 CRP 注射的小鼠的死亡率高于用野生型 CRP 注射的小鼠。存活率下降是由于用突变型 CRP 处理的小鼠的菌血症增加所致。我们的结论是 CRP 上的磷酸胆碱结合口袋对于 CRP 介导的小鼠对抗致死性肺炎球菌感染的初始保护是必需的。