Self-Assembled Ti4+@Biospore Microspheres for Sensitive DNA Analysis

被引:12
作者
Fei, Rui-Hua [1 ,2 ]
Tan, Chen [1 ]
Huang, Yue [1 ,2 ]
Chen, Huan-Chun [1 ]
Guo, Ai-Zhen [1 ]
Wang, Hai-Lin [3 ]
Hu, Yong-Gang [1 ,2 ]
机构
[1] Huazhong Agr Univ, State Key Lab Agr Microbiol, Wuhan 430070, Hubei, Peoples R China
[2] Huazhong Agr Univ, Coll Life Sci & Technol, Wuhan 430070, Hubei, Peoples R China
[3] Chinese Acad Sci, State Key Lab Environm Chem & Ecotoxicol, Ecoenvironm Sci Res Ctr, Beijing 100085, Peoples R China
基金
中国国家自然科学基金;
关键词
spore; biomaterials; Ti4+; adsorption; DNA analysis; GRAPHENE OXIDE; PHOTOCATALYTIC ACTIVITY; TITANIUM-DIOXIDE; NUCLEIC-ACIDS; NANOPARTICLES; OLIGONUCLEOTIDES; BIOSENSORS; SENSOR; TIO2; NANOMATERIALS;
D O I
10.1021/acsami.7b10478
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Ti4+ can be chemically adsorbed and assembled on the surface of the modified spore to form highly monodispersed Ti4+@spore microspheres. Moreover, we for the first time found that these biomicrospheres exhibit differential affinities toward ssDNA and dsDNA. As a principle-of-proof, we exploited the self-assembled Ti4+@spore microspheres for a hybridization analysis. Interestingly, in the hybridization analysis, residual ssDNA probes are selectively adsorbed on Ti4+@spore microspheres at pH 5.0 and then removed via centrifugation. By taking advantage of this property, the signal-to-noise ratio for DNA analysis was considerably increased by reducing the noise caused by the residual ssDNA probes. The proposed method features easy operation, high specificity, and sensitivity and thus exhibits potential for further applications on DNA biosensing.
引用
收藏
页码:34696 / 34705
页数:10
相关论文
共 55 条
[1]   Highly Sensitive DNA Sensor Based on Upconversion Nanoparticles and Graphene Oxide [J].
Alonso-Cristobal, P. ;
Vilela, P. ;
El-Sagheer, A. ;
Lopez-Cabarcos, E. ;
Brown, T. ;
Muskens, O. L. ;
Rubio-Retama, J. ;
Kanaras, A. G. .
ACS APPLIED MATERIALS & INTERFACES, 2015, 7 (23) :12422-12429
[2]   Ultra-high-density 3D DNA arrays within nanoporous biocompatible membranes for single-molecule-level detection and purification of circulating nucleic acids [J].
Aramesh, M. ;
Shimoni, O. ;
Fox, K. ;
Karle, T. J. ;
Lohrmann, A. ;
Ostrikov, K. ;
Prawer, S. ;
Cervenka, J. .
NANOSCALE, 2015, 7 (14) :5998-6006
[3]  
Baaske MD, 2014, NAT NANOTECHNOL, V9, P933, DOI [10.1038/nnano.2014.180, 10.1038/NNANO.2014.180]
[4]   A label-free fluorescent molecular beacon based on DNA-Ag nanoclusters for the construction of versatile Biosensors [J].
Cao, Qiao ;
Teng, Ye ;
Yang, Xuan ;
Wang, Jin ;
Wang, Erkang .
BIOSENSORS & BIOELECTRONICS, 2015, 74 :318-321
[5]   Phosphate adsorption properties of magnetite-based nanoparticles [J].
Daou, T. J. ;
Begin-Colin, S. ;
Greneche, J. M. ;
Thomas, F. ;
Derory, A. ;
Bernhardt, P. ;
Legare, P. ;
Pourroy, G. .
CHEMISTRY OF MATERIALS, 2007, 19 (18) :4494-4505
[6]   Fluorescence Resonance Energy Transfer between Quantum Dots and Graphene Oxide for Sensing Biomolecules [J].
Dong, Haifeng ;
Gao, Wenchao ;
Yan, Feng ;
Ji, Hanxu ;
Ju, Huangxian .
ANALYTICAL CHEMISTRY, 2010, 82 (13) :5511-5517
[7]   New Perspectives on Nanomaterial Aquatic Ecotoxicity: Production Impacts Exceed Direct Exposure Impacts for Carbon Nanotoubes [J].
Eckelman, Matthew J. ;
Mauter, Meagan S. ;
Isaacs, Jacqueline A. ;
Elimelech, Menachem .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2012, 46 (05) :2902-2910
[8]   A label-free biosensor for DNA detection based on ligand-responsive G-quadruplex formation [J].
Guo, Yahui ;
Xu, Pei ;
Hu, Hui ;
Zhou, Xiaodong ;
Hu, Jiming .
TALANTA, 2013, 114 :138-142
[9]   Artificial Receptors for the Recognition of Phosphorylated Molecules [J].
Hargrove, Amanda E. ;
Nieto, Sonia ;
Zhang, Tianzhi ;
Sessler, Jonathan L. ;
Anslyn, Eric V. .
CHEMICAL REVIEWS, 2011, 111 (11) :6603-6782
[10]   A Graphene Nanoprobe for Rapid, Sensitive, and Multicolor Fluorescent DNA Analysis [J].
He, Shijiang ;
Song, Bo ;
Li, Di ;
Zhu, Changfeng ;
Qi, Wenpeng ;
Wen, Yanqin ;
Wang, Lihua ;
Song, Shiping ;
Fang, Haiping ;
Fan, Chunhai .
ADVANCED FUNCTIONAL MATERIALS, 2010, 20 (03) :453-459