DNA Aptamer Assembly as a Vascular Endothelial Growth Factor Receptor Agonist

被引:50
作者
Ramaswamy, Vidhya [1 ]
Monsalve, Adam [1 ]
Sautina, Larysa [2 ]
Segal, Mark S. [2 ,5 ]
Dobson, Jon [1 ,3 ,4 ]
Allen, Josephine B. [1 ,4 ]
机构
[1] Univ Florida, Dept Mat Sci & Engn, Gainesville, FL 32611 USA
[2] Univ Florida, Coll Med, Div Nephrol, Gainesville, FL 32611 USA
[3] Univ Florida, J Crayton Pruitt Family Dept Biomed Engn, Gainesville, FL 32611 USA
[4] Univ Florida, Inst Cellular Engn & Regenerat Med, Gainesville, FL 32611 USA
[5] North Florida South Georgia Vet Hlth Syst, Gainesville, FL USA
基金
美国国家科学基金会;
关键词
EXPONENTIAL ENRICHMENT; SYSTEMATIC EVOLUTION; SIGNAL-TRANSDUCTION; LIGANDS; VEGF; SELECTION; BINDING; INTERNALIZATION; THERAPEUTICS; INHIBITION;
D O I
10.1089/nat.2014.0519
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Controlling receptor-mediated processes in cells is paramount in many research areas. The activity of small molecules and growth factors is difficult to control and can lead to off-target effects through the activation of nonspecific receptors as well as binding affinity to nonspecific cell types. In this study, we report the development of a molecular trigger in the form of a divalent nucleic acid aptamer assembly toward vascular endothelial growth factor receptor-2 (VEGFR2). The assembly binds to VEGFR2 and functions as a receptor agonist with targeted receptor binding, promoting receptor phosphorylation, activation of the downstream Akt pathway, upregulation of endothelial nitric oxide synthase, and endothelial cell capillary tube formation. The agonist action we report makes this aptamer construct a promising strategy to control VEGFR2-mediated cell signaling.
引用
收藏
页码:227 / 234
页数:8
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