Laboratory of GlycoNanotechnology, CIC biomaGUNE/CIBER-BBN, P degrees Miramón 182, San Sebastián E-20009, Spain.
Bioorg Med Chem Lett. 2010 May 1;20(9):2718-21. doi: 10.1016/j.bmcl.2010.03.079. Epub 2010 Mar 25.
Gold nanoparticles coated with multiple copies of an amphiphilic sulfate-ended ligand are able to bind the HIV envelope glycoprotein gp120 as measured by surface plasmon resonance (SPR) and inhibit in vitro the HIV infection of T-cells at nanomolar concentrations. A 50% density of sulfated ligands on approximately 2 nm nanoparticles (the other ligands being inert glucose derivatives) is enough to achieve high anti-HIV activities. This result opens up the possibility of tailoring both sulfated ligands and other anti-HIV molecules on the same gold cluster, thus contributing to the development of non-cocktail based multifunctional anti-HIV systems.
金纳米粒子表面覆盖有多拷贝的两亲性硫酸酯末端配体,可与 HIV 包膜糖蛋白 gp120 结合,这一作用可通过表面等离子体共振(SPR)来测量,并可在纳摩尔浓度下抑制 T 细胞的 HIV 感染。大约 2nm 金纳米粒子上 50%密度的硫酸酯配体(其余配体为惰性葡萄糖衍生物)足以实现高抗 HIV 活性。这一结果为在同一金簇上修饰硫酸酯配体和其他抗 HIV 分子开辟了可能性,从而有助于开发基于非鸡尾酒的多功能抗 HIV 系统。