Author/Authors :
Santosh Kumar ، نويسنده , , Won-Tak Choi، نويسنده , , Chang-Zhi Dong، نويسنده , , Navid Madani، نويسنده , , Shaomin Tian، نويسنده , , DongXiang Liu، نويسنده , , Youli Wang، نويسنده , , James Pesavento، نويسنده , , Jun Wang، نويسنده , , Xuejun Fan، نويسنده , , Jian Yuan، نويسنده , , Wayne R. Fritzsche، نويسنده , , Jing An، نويسنده , , Joseph G. Sodroski، نويسنده , , Douglas D. Richman، نويسنده , , Ziwei Huang، نويسنده ,
Abstract :
Chemokines and their receptors play important roles in numerous physiological and pathological processes. To develop natural chemokines into receptor probes and inhibitors of pathological processes, the lack of chemokine-receptor selectivity must be overcome. Here, we apply chemical synthesis and the concept of modular modifications to generate unnatural synthetically and modularly modified (SMM)-chemokines that have high receptor selectivity and affinity, and reduced toxicity. A proof of the concept was shown by transforming the nonselective viral macrophage inflammatory protein-II into new analogs with enhanced selectivity and potency for CXCR4 or CCR5, two principal coreceptors for human immunodeficiency virus (HIV)-1 entry. These new analogs provided insights into receptor binding and signaling mechanisms and acted as potent HIV-1 inhibitors. These results support the concept of SMM-chemokines for studying and controlling the function of other chemokine receptors.