Herrmann J L, Delahay R, Gallagher A, Robertson B, Young D
Department of Infectious Diseases and Microbiology, Imperial College School of Medicine, St. Mary's Campus, Norfolk Place, W2 1PG, London, UK.
FEBS Lett. 2000 May 19;473(3):358-62. doi: 10.1016/s0014-5793(00)01553-2.
A recombinant expression system was developed to analyse sequence determinants involved in O-glycosylation of proteins in mycobacteria. By expressing peptide sequences corresponding to known glycosylation sites within a chimeric lipoprotein construct, amino acids flanking modified threonine residues were found to have an important influence on glycosylation. The expression system was used to screen mycobacterial sequences selected using a neural network (NetOglyc) trained on eukaryotic O-glycoproteins. Evidence of glycosylation was obtained for eight of 11 proteins tested. The results suggest that sites involved in O-glycosylation of mycobacterial and eukaryotic proteins share similar structural features.
开发了一种重组表达系统,以分析分枝杆菌中蛋白质O-糖基化所涉及的序列决定因素。通过在嵌合脂蛋白构建体中表达与已知糖基化位点相对应的肽序列,发现修饰苏氨酸残基两侧的氨基酸对糖基化有重要影响。该表达系统用于筛选使用在真核O-糖蛋白上训练的神经网络(NetOglyc)选择的分枝杆菌序列。在测试的11种蛋白质中有8种获得了糖基化证据。结果表明,分枝杆菌和真核蛋白质的O-糖基化所涉及的位点具有相似的结构特征。