Secchi Massimiliano, Longhi Renato, Vassena Lia, Sironi Francesca, Grzesiek Stephan, Lusso Paolo, Vangelista Luca
Division of Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute, Via Olgettina 58, Milan 20132, Italy.
Chem Biol. 2012 Dec 21;19(12):1579-88. doi: 10.1016/j.chembiol.2012.10.007.
CCR5, the major HIV-1 coreceptor, is a primary target for HIV-1 entry inhibition strategies. CCL5/RANTES, a natural CCR5 ligand, is one of the most potent HIV-1 entry inhibitors and, therefore, an ideal candidate to derive HIV-1 blockers. Peptides spanning the RANTES N-loop/β1-strand region act as specific CCR5 antagonists, with their hydrophobic N- and C termini playing a crucial role in virus blockade. Here, hydrophobic surfaces were enhanced by tryptophan substitution of aromatic residues, highlighting position 27 as a critical hot spot for HIV-1 blockade. In a further molecular evolution step, C-terminal engraftment of RANTES 40' loop produced a peptide with the highest solubility and anti-HIV-1 activity. These modified peptides represent leads for the development of effective HIV-1 inhibitors and microbicides.
CCR5是主要的HIV-1共受体,是HIV-1进入抑制策略的主要靶点。CCL5/趋化因子调节激活正常T细胞表达和分泌因子(RANTES)是一种天然的CCR5配体,是最有效的HIV-1进入抑制剂之一,因此是衍生HIV-1阻断剂的理想候选物。跨越RANTES N环/β1链区域的肽作为特异性CCR5拮抗剂,其疏水的N端和C端在病毒阻断中起关键作用。在此,通过色氨酸取代芳香族残基增强了疏水表面,突出了27位是HIV-1阻断的关键热点。在进一步的分子进化步骤中,RANTES 40'环的C端嫁接产生了一种具有最高溶解度和抗HIV-1活性的肽。这些修饰的肽是开发有效HIV-1抑制剂和杀微生物剂的先导物。