Siemion I Z, Słoń J, Nawrocka E, Wieczorek Z
Institute of Chemistry, Wrocław University, Poland.
Int J Pept Protein Res. 1990 May;35(5):428-33. doi: 10.1111/j.1399-3011.1990.tb00069.x.
The syntheses of HBV S-protein partial sequences: Thr-Lys-Pro-Thr (I), Thr-Lys-Pro-Thr-Asp (II), and Thr-Lys-Pro-Thr-Asp-Gly (III) and also of pentapeptide Thr-Lys-Pro-Gly-Arg (IV), are described. For the peptides II and III inhibitory activity against tuftsin was found. Peptide IV (an analogue of tuftsin-inhibitor Thr-Lys-Pro-Pro-Arg) demonstrated a tuftsin-like activity in the phagocytosis experiments.
描述了乙肝病毒表面抗原(HBV S-protein)部分序列:苏氨酸-赖氨酸-脯氨酸-苏氨酸(I)、苏氨酸-赖氨酸-脯氨酸-苏氨酸-天冬氨酸(II)和苏氨酸-赖氨酸-脯氨酸-苏氨酸-天冬氨酸-甘氨酸(III)以及五肽苏氨酸-赖氨酸-脯氨酸-甘氨酸-精氨酸(IV)的合成。发现肽II和III对促吞噬肽有抑制活性。在吞噬作用实验中,肽IV(促吞噬肽抑制剂苏氨酸-赖氨酸-脯氨酸-脯氨酸-精氨酸的类似物)表现出类似促吞噬肽的活性。