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人唾液中的24种富组蛋白(组蛋白3片段)级联反应。分泌前序列切割途径的相关推测。

A cascade of 24 histatins (histatin 3 fragments) in human saliva. Suggestions for a pre-secretory sequential cleavage pathway.

作者信息

Castagnola Massimo, Inzitari Rosanna, Rossetti Diana Valeria, Olmi Chiara, Cabras Tiziana, Piras Vincenzo, Nicolussi Paola, Sanna Maria Teresa, Pellegrini Mariagiuseppina, Giardina Bruno, Messana Irene

机构信息

Istituto di Biochimica e Biochimica Clinica, Facoltà di Medicina, Università Cattolica, Roma, Italy.

出版信息

J Biol Chem. 2004 Oct 1;279(40):41436-43. doi: 10.1074/jbc.M404322200. Epub 2004 Jul 21.

Abstract

The systematic search by tandem mass spectrometry of human saliva from four different subjects, of 136 possible fragments originated from histatin 3, allowed the detection of 24 different peptides. They include, with the exception of histatin 4, all the known histatin 3 fragments, namely histatins 5-12 and the peptides corresponding to 15-24, 26-32, 29-32 residues, and 13 new fragments corresponding to 1-11, 1-12, 1-13, 5-13, 6-11, 6-13, 7-11, 7-12, 7-13, 14-24, 14-25, 15-25, and 28-32 residues of histatin 3. On the contrary, none of 119 possible fragments of histatin 1, including histatin 2, was detected. The results suggest that the genesis of histatin 3-related peptides, being under the principal action of trypsin-like activities, is probably not a random process but rather follows a sequential fragmentation pathway. Lack of detection of C-terminal fragments, with the exception of 26-32, 28-32, and 29-32 fragments, suggested that arginine 25 should be the first cleavage site, generating histatin 6 and 26-32 fragments. The genesis of 28-32 and 29-32 fragments and histatin 5 should implicate a subsequent exo-protease action. Similarly, lack of detection of fragments having Lys-5 and Arg-6 at the N terminus and Arg-25 at the C terminus strongly suggested that sequences KRKF (11-14 residues) and AKR (4-6 residues) should be the second and the third cleavage sites, respectively. Lys-17 and Arg-22 are not cleaved at all.

摘要

通过串联质谱对来自四个不同受试者的人类唾液进行系统搜索,在136个可能源自组蛋白3的片段中,检测到了24种不同的肽。除组蛋白4外,它们包括所有已知的组蛋白3片段,即组蛋白5 - 12以及对应于15 - 24、26 - 32、29 - 32个残基的肽,还有13个对应于组蛋白3的1 - 11、1 - 12、1 - 13、5 - 13、6 - 11、6 - 13、7 - 11、7 - 12、7 - 13、14 - 24、14 - 25、15 - 25和28 - 32个残基的新片段。相反,在包括组蛋白2在内的119个组蛋白1的可能片段中,未检测到任何片段。结果表明,组蛋白3相关肽的产生可能并非随机过程,而是在类胰蛋白酶活性的主要作用下遵循顺序裂解途径。除了26 - 32、28 - 32和29 - 32片段外,未检测到C端片段,这表明精氨酸25应该是第一个裂解位点,产生组蛋白6和26 - 32片段。28 - 32和29 - 32片段以及组蛋白5的产生应该涉及随后的外切蛋白酶作用。同样,未检测到在N端具有赖氨酸 - 5和精氨酸 - 6以及在C端具有精氨酸 - 25的片段,这强烈表明序列KRKF(11 - 14个残基)和AKR(4 - 6个残基)应该分别是第二个和第三个裂解位点。赖氨酸 - 17和精氨酸 - 22根本不被裂解。

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