School of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia, Queensland 4072, Australia.
Bioorg Med Chem Lett. 2011 Oct 1;21(19):5863-5. doi: 10.1016/j.bmcl.2011.07.102. Epub 2011 Aug 2.
Stimulation of toll-like receptor 2 (TLR2) by bacterial lipoproteins induces fast non-specific immune responses against pathogens followed by slow but specific adaptive immune responses. Development of synthetic TLR2 agonists/antagonists would be useful in the prevention of different infectious and immunologic disorders. The current study reports synthesis and TLR2 activity of two simple TLR2 ligands, which feature minimal structural requirement for TLR2 activity (two long lipid chains) and stimulate agonistic activity at nanomolar concentration.
细菌脂蛋白刺激 Toll 样受体 2(TLR2)可诱导针对病原体的快速非特异性免疫应答,随后是缓慢但特异性的适应性免疫应答。合成 TLR2 激动剂/拮抗剂的开发将有助于预防不同的感染和免疫紊乱。本研究报告了两种简单 TLR2 配体的合成和 TLR2 活性,它们具有 TLR2 活性的最小结构要求(两条长脂质链),并以纳摩尔浓度刺激激动活性。