Su C J, Tryon V V, Baseman J B
Department of Microbiology, University of Texas Health Science Center at San Antonio 78284.
Infect Immun. 1987 Dec;55(12):3023-9. doi: 10.1128/iai.55.12.3023-3029.1987.
Mycoplasma pneumoniae cytadhesin P1 was purified by monoclonal antibody affinity chromatography followed by preparative sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The N-terminal 18-amino-acid sequence of P1 was determined and used to design two synthetic oligonucleotides, a 14-mer corresponding to amino acids 1 to 5 and an 18-mer corresponding to amino acids 7 to 12. These oligonucleotides served as hybridization probes for the identification of the P1 gene by Southern blot analysis of M. pneumoniae DNA. The P1 gene was cloned into plasmid pUC19 and mapped by using appropriate restriction endonucleases. The DNA sequence of the entire P1 gene was determined by subcloning appropriate DNA fragments into bacteriophage M13 and sequencing the DNA by the dideoxy-chain-termination method. The P1 gene contains an open reading frame of 4,881 nucleotides coding for a protein of 1,627 amino acids with a calculated molecular weight of 176,288. Properties of the amino-terminal sequence suggest that protein P1 may be synthesized as a precursor with subsequent processing to a mature protein of a calculated molecular weight of 169,758. Potential antigenic sites were determined by hydrophilicity plots. A computer search revealed that part of the predicted P1 sequence is homologous to cytoskeletal keratin of mammalian species and human fibrinogen alpha chain precursor. These results demonstrate the uniqueness of P1 as a cytadhesin and virulence determinant.
肺炎支原体细胞黏附素P1通过单克隆抗体亲和层析,随后进行制备性十二烷基硫酸钠-聚丙烯酰胺凝胶电泳进行纯化。测定了P1的N端18个氨基酸序列,并用于设计两条合成寡核苷酸,一条14聚体对应于氨基酸1至5,一条18聚体对应于氨基酸7至12。这些寡核苷酸用作杂交探针,通过肺炎支原体DNA的Southern印迹分析来鉴定P1基因。将P1基因克隆到质粒pUC19中,并使用合适的限制性内切酶进行定位。通过将合适的DNA片段亚克隆到噬菌体M13中,并通过双脱氧链终止法对DNA进行测序,确定了整个P1基因的DNA序列。P1基因包含一个4881个核苷酸的开放阅读框,编码一个1627个氨基酸的蛋白质,计算分子量为176288。氨基端序列的特性表明,蛋白质P1可能以前体形式合成,随后加工成计算分子量为169758的成熟蛋白质。通过亲水性图谱确定潜在的抗原位点。计算机搜索显示,预测的P1序列的一部分与哺乳动物物种的细胞骨架角蛋白和人纤维蛋白原α链前体同源。这些结果证明了P1作为细胞黏附素和毒力决定因素的独特性。