Zeltins Andris, Turks Māris, Skrastina Dace, Lugiņina Jevgeņija, Kalnciema Ieva, Balke Ina, Bizdēna Ērika, Skrivelis Vitalijs
Latvian Biomedical Research and Study Centre, Ratsupites 1, LV-1067 Riga, Latvia.
Institute of Technology of Organic Chemistry, Riga Technical University, P. Valdena Str. 3, LV-1048 Riga, Latvia.
Antibiotics (Basel). 2017 Sep 11;6(3):18. doi: 10.3390/antibiotics6030018.
Milbemycins are macrolide antibiotics with a broad spectrum of nematocidal, insecticidal, and acaricidal activity. To obtain milbemycin A₃/A₄ derivatives suitable for chemical conjugation to protein carriers (milbemycin haptens), succinate linker and a novel 17-atom-long linker containing a terminal carboxylic acid group were attached to the milbemycin core in a protecting group-free synthesis. The obtained milbemycin A₃/A₄ derivatives were coupled to Potato virus Y-like nanoparticles by the activated ester method. The reaction products were characterized and used in mice immunization experiments. It was found that the mice developed weak specific immune responses toward all tested milbemycin haptens.
米尔倍霉素是一类具有广泛杀线虫、杀虫和杀螨活性的大环内酯类抗生素。为了获得适合与蛋白质载体化学偶联的米尔倍霉素A₃/A₄衍生物(米尔倍霉素半抗原),在无保护基团的合成中,将琥珀酸连接子和一个含有末端羧酸基团的新型17原子长连接子连接到米尔倍霉素核心上。通过活化酯法将得到的米尔倍霉素A₃/A₄衍生物与马铃薯Y病毒样纳米颗粒偶联。对反应产物进行了表征并用于小鼠免疫实验。结果发现,小鼠对所有测试的米尔倍霉素半抗原产生了较弱的特异性免疫反应。