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b型流感嗜血杆菌外膜蛋白P5和P6的纯化及部分特性分析

Purification and partial characterization of outer membrane proteins P5 and P6 from Haemophilus influenzae type b.

作者信息

Munson R S, Granoff D M

出版信息

Infect Immun. 1985 Sep;49(3):544-9. doi: 10.1128/iai.49.3.544-549.1985.

Abstract

The major outer membrane proteins of Haemophilus influenzae type b (Hib), designated P5 and P6 (R.S. Munson, Jr., J.L. Shenep, S.J. Barenkamp, and D.M. Granoff, J. Clin. Invest. 72:677-684, 1983), were purified to homogeneity and partially characterized. P5 was insoluble in octylglucoside-NaCl and could be extracted with 1% sodium dodecyl sulfate (SDS) in 20 mM phosphate (pH 7.5). Solubilized P5 was further purified on hydroxylapatite in 0.1% SDS. The purified protein had an apparent molecular weight of 27,000 as determined by SDS-polyacrylamide gel electrophoresis after sample preparation at room temperature. The protein migrated with an apparent molecular weight of 35,000 after heating for 30 min at 100 degrees C in the presence of 10% beta-mercaptoethanol (beta ME). Rabbit antisera prepared against the purified preparation immunoprecipitated solubilized protein P5 but had no protective activity in the infant rat bacteremic model. The SDS-insoluble residue was further extracted with 1% SDS-0.5 M NaCl-0.1% beta ME at 37 degrees C. A single outer membrane protein, designated P6, with an apparent molecular weight of 16,000, remained insoluble under these conditions. Antiserum prepared against this insoluble fraction contained antibodies which, after removal of anti-lipopolysaccharide antibody, immunoprecipitated P6 and protected infant rats challenged with Hib. Protein P6 could be released from the insoluble cell wall in the presence of SDS-NaCl-beta ME at 60 degrees C. Thus, proteins P5 and P6 could be purified from the cell envelope of Hib. Based on the results from infant rat passive protection experiments, antigens in the P6-cell wall fraction merit further investigation as possible vaccine components. In contrast, epitopes on protein P5 did not appear to elicit protective antibody.

摘要

b型流感嗜血杆菌(Hib)的主要外膜蛋白,命名为P5和P6(R.S.芒森,小J.L.谢内普,S.J.巴伦坎普,和D.M.格拉诺夫,《临床研究杂志》72:677 - 684,1983),被纯化至同质并进行了部分特性分析。P5不溶于辛基葡糖苷 - 氯化钠,可用20 mM磷酸盐(pH 7.5)中的1%十二烷基硫酸钠(SDS)提取。溶解的P5在0.1% SDS的羟基磷灰石上进一步纯化。经室温样品制备后,通过SDS - 聚丙烯酰胺凝胶电泳测定,纯化后的蛋白表观分子量为27,000。在10%β - 巯基乙醇(βME)存在下于100℃加热30分钟后,该蛋白迁移时的表观分子量为35,000。针对纯化制剂制备的兔抗血清能免疫沉淀溶解的蛋白P5,但在幼鼠菌血症模型中没有保护活性。SDS不溶性残渣在37℃用1% SDS - 0.5 M氯化钠 - 0.1%βME进一步提取。一种表观分子量为16,000的单一外膜蛋白,命名为P6,在这些条件下仍不溶解。针对该不溶性部分制备的抗血清含有抗体,去除抗脂多糖抗体后,能免疫沉淀P6并保护受到Hib攻击的幼鼠。在60℃,SDS - 氯化钠 - βME存在的情况下,蛋白P6可从不溶性细胞壁中释放出来。因此,蛋白P5和P6可从Hib的细胞膜中纯化出来。基于幼鼠被动保护实验的结果,P6 - 细胞壁部分的抗原作为可能的疫苗成分值得进一步研究。相比之下,蛋白P5上的表位似乎不会引发保护性抗体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e18/261198/e35827fa694a/iai00114-0093-a.jpg

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