Ligand binding affinity and changes in the lateral diffusion of receptor for advanced glycation endproducts (RAGE)
Ligand binding affinity and changes in the lateral diffusion of receptor for advanced glycation endproducts (RAGE)
复制标题
配体结合亲和力和晚期糖基化终产物受体横向扩散的变化 (RAGE)
DOI：
10.1016/j.bbamem.2016.10.001
复制
发表时间：
2016
期刊：
影响因子：
--
通讯作者：
Smith, Emily A.
中科院分区：
文献类型：
--
作者：
Syed, Aleem;Zhu, Qiaochu;Smith, Emily A.
The effect of ligand on the lateral diffusion of receptor for advanced glycation endproducts (RAGE), a receptor involved in numerous pathological conditions, remains unknown. Single particle tracking experiments that use quantum dots specifically bound to hemagglutinin (HA)-tagged RAGE (HA-RAGE) are reported to elucidate the effect of ligand binding on HA-RAGE diffusion in GM07373 cell membranes. The ligand used in these studies is methylglyoxal modified-bovine serum albumin (MGO-BSA) containing advanced glycation end products modifications. The binding affinity between soluble RAGE and MGO-BSA increases by 1.8 to 9.7-fold as the percent primary amine modification increases from 24 to 74% and with increasing negative charge on the MGO-BSA. Ligand incubation affects the HA-RAGE diffusion coefficient, the radius of confinement, and duration of confinement. There is, however, no correlation between MGO-BSA ligand binding affinity with soluble RAGE and the extent of the changes in HA-RAGE lateral diffusion. The ligand induced changes to HA-RAGE lateral diffusion do not occur when cholesterol is depleted from the cell membrane, indicating the mechanism for ligand-induced changes to HA-RAGE diffusion is cholesterol dependent. The results presented here serve as a first step in unraveling how ligand influences RAGE lateral diffusion.
