Nonstatistical binding of a protein to clustered carbohydrates
收藏PubMed Central1999-10-12 更新2026-04-25 收录
下载链接:
https://pmc.ncbi.nlm.nih.gov/articles/PMC18363/
下载链接
链接失效反馈官方服务:
资源简介:
Carbohydrate-derivatized self-assembled monolayers (SAMs) are used as a model system to address issues involving cell-surface carbohydrate–protein interactions. Here we examine the influence of carbohydrate surface density on protein-binding avidity. We show that the binding selectivity of Bauhinia purpurea lectin switches from one carbohydrate ligand to another as the surface density of the carbohydrate ligands increases from values of χ(sugar) ≈ 0.1–1.0. Polyvalent binding is possible at all surface densities investigated; hence, the switch in selectivity is not due simply to the achievement of a critical density that permits polyvalent contacts. Instead, secondary interactions at high surface densities promote a switch in carbohydrate-binding selectivity. These findings may have implications for how changes in the composition and the density of cell-surface carbohydrates influence biological recognition processes and regulatory pathways.
提供机构:
National Academy of Sciences
创建时间:
1999-10-12



