EPH受体A2
以法林
受体
DNA折纸
化学
细胞生物学
生物物理学
配体(生物化学)
功能(生物学)
生物
DNA
生物化学
受体酪氨酸激酶
作者
Alan Shaw,Vanessa Lundin,Ekaterina Petrova,Ferenc Fördős,Erik Benson,Rasel A. Al-Amin,Anna Herland,Andries Blokzijl,Björn Högberg,Ana I. Teixeira
出处
期刊:Nature Methods
[Springer Nature]
日期:2014-07-06
卷期号:11 (8): 841-846
被引量:241
摘要
Ligand nanocalipers made using DNA nanotechnology are used to display ephrin-A5 at well-defined spatial intervals to study how nanoscale ligand spacing affects EphA2 receptor activation in breast cancer cells. The spatial organization of membrane-bound ligands is thought to regulate receptor-mediated signaling. However, direct regulation of receptor function by nanoscale distribution of ligands has not yet been demonstrated, to our knowledge. We developed rationally designed DNA origami nanostructures modified with ligands at well-defined positions. Using these 'nanocalipers' to present ephrin ligands, we showed that the nanoscale spacing of ephrin-A5 directs the levels of EphA2 receptor activation in human breast cancer cells. Furthermore, we found that the nanoscale distribution of ephrin-A5 regulates the invasive properties of breast cancer cells. Our ligand nanocaliper approach has the potential to provide insight into the roles of ligand nanoscale spatial distribution in membrane receptor–mediated signaling.
科研通智能强力驱动
Strongly Powered by AbleSci AI