Diamond G, Zasloff M, Eck H, Brasseur M, Maloy W L, Bevins C L
Division of Human Genetics and Molecular Biology, Children's Hospital of Philadelphia, PA 19104.
Proc Natl Acad Sci U S A. 1991 May 1;88(9):3952-6. doi: 10.1073/pnas.88.9.3952.
Extracts of the bovine tracheal mucosa have an abundant peptide with potent antimicrobial activity. The 38-amino acid peptide, which we have named tracheal antimicrobial peptide (TAP), was isolated by a sequential use of size-exclusion, ion-exchange, and reverse-phase chromatographic fractionations using antimicrobial activity as a functional assay. The yield was approximately 2 micrograms/g of wet mucosa. The complete peptide sequence was determined by a combination of peptide and cDNA analysis. The amino acid sequence of TAP is H-Asn-Pro-Val-Ser-Cys-Val-Arg-Asn-Lys-Gly-Ile-Cys-Val-Pro-Ile-Arg-Cys-Pr o- Gly-Ser-Met-Lys-Gln-Ile-Gly-Thr-Cys-Val-Gly-Arg-Ala-Val-Lys-Cys-Cys-Arg- Lys-Lys - OH. Mass spectral analysis of the isolated peptide was consistent with this sequence and indicated the participation of six cysteine residues in the formation of intramolecular disulfide bonds. The size, basic charge, and presence of three intramolecular disulfide bonds is similar to, but clearly distinct from, the defensins, a well-characterized class of antimicrobial peptides from mammalian circulating phagocytic cells. The putative TAP precursor is predicted to be relatively small (64 amino acids), and the mature peptide resides at the extreme carboxyl terminus and is bracketed by a short putative propeptide region and an inframe stop codon. The mRNA encoding this peptide is more abundant in the respiratory mucosa than in whole lung tissue. The purified peptide had antibacterial activity in vitro against Escherichia coli, Staphylococcus aureus, Klebsiella pneumonia, and Pseudomonas aeruginosa. In addition, the peptide was active against Candida albicans, indicating a broad spectrum of activity. This peptide appears to be, based on structure and activity, a member of a group of cysteine-rich, cationic, antimicrobial peptides found in animals, insects, and plants. The isolation of TAP from the mammalian respiratory mucosa may provide insight into our understanding of host defense of this vital tissue.
牛气管黏膜提取物含有一种具有强大抗菌活性的丰富肽段。我们将这种38个氨基酸的肽段命名为气管抗菌肽(TAP),通过依次使用尺寸排阻、离子交换和反相色谱分级分离,并以抗菌活性作为功能检测方法将其分离出来。产量约为每克湿黏膜2微克。通过肽段分析和cDNA分析相结合的方法确定了完整的肽段序列。TAP的氨基酸序列为H-Asn-Pro-Val-Ser-Cys-Val-Arg-Asn-Lys-Gly-Ile-Cys-Val-Pro-Ile-Arg-Cys-Pro-Gly-Ser-Met-Lys-Gln-Ile-Gly-Thr-Cys-Val-Gly-Arg-Ala-Val-Lys-Cys-Cys-Arg-Lys-Lys-OH。对分离得到的肽段进行质谱分析,结果与该序列一致,并表明六个半胱氨酸残基参与了分子内二硫键的形成。其大小、碱性电荷以及三个分子内二硫键的存在与防御素相似,但又明显不同,防御素是一类来自哺乳动物循环吞噬细胞的特征明确的抗菌肽。推测的TAP前体预计相对较小(64个氨基酸),成熟肽位于极端羧基末端,两侧分别是一个短的推测前肽区和一个符合读框的终止密码子。编码该肽段的mRNA在呼吸道黏膜中的含量比在全肺组织中更丰富。纯化后的肽段在体外对大肠杆菌、金黄色葡萄球菌、肺炎克雷伯菌和铜绿假单胞菌具有抗菌活性。此外,该肽段对白色念珠菌也有活性,表明其具有广泛的活性谱。基于结构和活性,这种肽段似乎是在动物、昆虫和植物中发现的一组富含半胱氨酸、阳离子抗菌肽中的一员。从哺乳动物呼吸道黏膜中分离出TAP可能有助于我们深入了解这个重要组织的宿主防御机制。