Visualization of single multivalent receptor-ligand complexes by transmission electron microscopy

被引:0
|
作者
Gestwicki, JE
Strong, LE
Kiessling, LL
机构
[1] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Biochem, Madison, WI 53706 USA
关键词
aggregation; electron microscopy; lectins; polyvalent ligands; ring-opening polymerization;
D O I
10.1002/1521-3773(20001215)39:24<4567::AID-ANIE4567>3.0.CO;2-F
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Gold nanoparticle labels enable the position of receptors (concanavalin A) bound to multivalent ligands (see picture; top: straptavidin-conjugated gold particles, middle: receptors, bottom: ligand) assembled using the ring-opening metathesis polymerization to be determined by transmission electron microscopy. The number of concanavalin A tetramers incorporated into the receptor-ligand complexes depends on the ligand valency. The results illustrate a general approach for the elucidation of the stoichiometry of individual multivalent ligand-receptor complexes, which is critical for understanding the mechanism of multivalent binding events.
引用
收藏
页码:4567 / +
页数:5
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