Self-assembled DNA-based giant thrombin nanoparticles for controlled release

被引:4
作者
Sung, Jong Hwan [1 ]
Han, Daehoon [2 ]
Lee, Jong Bum [2 ]
机构
[1] Hongik Univ, Dept Chem Engn, Seoul, South Korea
[2] Univ Seoul, Dept Chem Engn, Seoul 130743, South Korea
基金
新加坡国家研究基金会;
关键词
Aptamer; DNA; Protein delivery; Thrombin; DRUG-DELIVERY; PROTEIN; APTAMERS;
D O I
10.1002/biot.201200312
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Protein-aptamer interactions have been used in a wide range of fields, including medical diagnosis and protein delivery. Herein, we report a method for thrombin delivery with thrombin-binding aptamer (TBA), which is one of the well-known aptamers for thrombin, by generating giant thrombin nanoparticles (GTNPs). GTNPs can be synthesized by crosslinking thrombin with DNA nano structures that possess several TBA molecules. To generate GTNPs, two different DNA nano structures were used. Y-shaped DNA with TBA and X-shaped DNA with TBA were used for 250 and 650 nm GTNPs, respectively. Controlled release of thrombin from GTNPs was performed by adding complementary DNA (cDNA) to TBA. To investigate thrombin release from GTNPs, the sizes of the GTNPs were measured using dynamic light scattering, atomic force microscopy (AFM), and scanning electron microscopy (SEM). We confirmed a decrease in the size of GTNPs with various concentrations of cDNA, suggesting the release of thrombin. Based on these results, we expect that our method can be used to control the amount of thrombin released effectively. Our method is also widely applicable for effective protein delivery.
引用
收藏
页码:215 / 220
页数:6
相关论文
共 23 条
[1]   Controlled delivery of the anti-VEGF aptamer EYE001 with poly(lactic-co-glycolic) acid microspheres [J].
Carrasquillo, KG ;
Ricker, JA ;
Rigas, IK ;
Miller, JW ;
Gragoudas, ES ;
Adamis, AP .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 (01) :290-299
[2]   GREEN FLUORESCENT PROTEIN AS A MARKER FOR GENE-EXPRESSION [J].
CHALFIE, M ;
TU, Y ;
EUSKIRCHEN, G ;
WARD, WW ;
PRASHER, DC .
SCIENCE, 1994, 263 (5148) :802-805
[3]   Polysaccharide hydrogels for protein drug delivery [J].
Chen, J ;
Jo, S ;
Park, K .
CARBOHYDRATE POLYMERS, 1995, 28 (01) :69-76
[4]  
De M, 2009, NAT CHEM, V1, P461, DOI [10.1038/NCHEM.334, 10.1038/nchem.334]
[5]   Protein-based therapeutic approaches targeting death receptors [J].
French, LE ;
Tschopp, J .
CELL DEATH AND DIFFERENTIATION, 2003, 10 (01) :117-123
[6]   Percutaneous repair of abdominal aortic pseudoaneurysm by catheter-based delivery of thrombin [J].
Geckeis, K ;
Eggebrecht, H ;
Schmermund, A ;
Kühl, H ;
Niebel, W ;
Omlor, G ;
Erbel, R .
JOURNAL OF ENDOVASCULAR THERAPY, 2006, 13 (02) :264-268
[7]   Protein and RNA engineering to customize microbial molecular reporting [J].
Gredell, Joseph A. ;
Frei, Christopher S. ;
Cirino, Patrick C. .
BIOTECHNOLOGY JOURNAL, 2012, 7 (04) :477-499
[8]   A liposome-based nanostructure for aptamer directed delivery [J].
Kang, Huaizhi ;
O'Donoghue, Meghan B. ;
Liu, Haipeng ;
Tan, Weihong .
CHEMICAL COMMUNICATIONS, 2010, 46 (02) :249-251
[9]   Biodegradable polymeric nanoparticles based drug delivery systems [J].
Kumari, Avnesh ;
Yadav, Sudesh Kumar ;
Yadav, Subhash C. .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2010, 75 (01) :1-18
[10]  
Lee JB, 2009, NAT NANOTECHNOL, V4, P430, DOI [10.1038/NNANO.2009.93, 10.1038/nnano.2009.93]