Second generation of fucose-based DC-SIGN ligands: affinity improvement and specificity versus Langerin

被引:62
作者
Andreini, Manuel [2 ,3 ]
Doknic, Daniela [2 ,3 ]
Sutkeviciute, Ieva [1 ,6 ]
Reina, Jose J. [2 ,3 ]
Duan, Janxin [4 ]
Chabrol, Eric [1 ,6 ]
Thepaut, Michel [1 ,6 ,7 ]
Moroni, Elisabetta [2 ,3 ]
Doro, Fabio [2 ,3 ]
Belvisi, Laura [2 ,3 ]
Weiser, Joerg [4 ]
Rojo, Javier [5 ]
Fieschi, Franck [1 ,6 ,8 ]
Bernardi, Anna [2 ,3 ]
机构
[1] Univ Grenoble 1, Inst Biol Struct, F-38027 Grenoble, France
[2] Univ Milan, Dipartimento Chim Organ & Ind, I-20133 Milan, Italy
[3] CISI, I-20133 Milan, Italy
[4] Anterio Consult & Res, D-68165 Mannheim, Germany
[5] Univ Seville, CSIC, Glycosyst Lab, Inst Invest Quim, Seville 41092, Spain
[6] CNRS, UMR 5075, Grenoble, France
[7] CEA, Grenoble, France
[8] Inst Univ France, F-75005 Paris, France
关键词
C-TYPE LECTINS; DENDRITIC CELLS; STRUCTURAL BASIS; TRANS-INFECTION; HIV-1; TRANSMISSION; EBOLA-VIRUS; T-CELLS; BINDING; RECOGNITION; RECEPTORS;
D O I
10.1039/c1ob05573a
中图分类号
O62 [有机化学];
学科分类号
070303 [有机化学];
摘要
DC-SIGN and Langerin are two C-type lectins involved in the initial steps of HIV infections: the former acts as a viral attachment factor and facilitates viral invasion of the immune system, the latter has a protective effect. Potential antiviral compounds targeted against DC-SIGN were synthesized using a common fucosylamide anchor. Their DC-SIGN affinity was tested by SPR and found to be similar to that of the natural ligand Lewis-X (Le(X)). The compounds were also found to be selective for DC-SIGN and to interact only weakly with Langerin. These molecules are potentially useful therapeutic tools against sexually transmitted HIV infection.
引用
收藏
页码:5778 / 5786
页数:9
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