Abstract
Aptamers are oligonucleotides displaying specific binding properties for a predetermined target. They can be easily immobilized on various surfaces such as nanoparticles. Functionalized particles can then be used to various aims. We took advantage of the AlphaScreen® technology for monitoring aptamer-mediated interactions. A particle bearing an aptamer contains a photosensitizer whereas another type of particle contains a chemiluminescer. Irradiation causes the formation of singlet oxygen species in the photosensitizer-containing bead that in turn activates the chemiluminescer. Luminescence emission can be observed if the two types of beads are in close proximity (<200 nm). This is achieved when the cognate ligand of the aptamer is grafted onto the chemiluminescer-containing bead. Using this technology we have screened oligonucleotide libraries and monitored aptamer–protein interactions. This constitutes the basis for aptamer-based analytical assays.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Ellington AD, Szostak JW (1990) In vitro selection of RNA molecules that bind specific ligands. Nature 346:818–822
Tuerk C, Gold L (1990) Systematic evolution of ligands by exponential enrichment: RNA ligands to bacteriophage T4 DNA polymerase. Science 249:505–510
Jayasena SD (1999) Aptamers: An emerging class of molecules that rival antibodies in diagnostics. Clin Chem 45:1628–1650
Dausse E, Da Rocha Gomes S, Toulmé JJ (2009) Aptamers: a new class of oligonucleotides in the drug discovery pipeline? Curr Opin Pharmacol 9:602–607
Tombelli S, Mascini M (2009) Aptamers as molecular tools for bioanalytical methods. Curr Opin Mol Ther 11:179–188
Cibiel A, Pestourie C, Ducongé F (2012) In vivo uses of aptamers selected against cell surface biomarkers for therapy and molecular imaging. Biochimie 94:1595–1606
Kang KN, Lee YS (2013) RNA aptamers: a review of recent trends and applications. Adv Biochem Eng Biotechnol 131:153–169
Radom F, Jurek PM, Mazurek MP, Otlewski J, Jelen F (2013) Aptamers: molecules of great potential. Biotechnol Adv 31:1260–1274
Gold L, Ayers D, Bertino J, Bock C, Bock A, Brody EN, Carter J, Dalby AB, Eaton BE, Fitzwater T et al (2010) Aptamer-based multiplexed proteomic technology for biomarker discovery. PLoS One 5:e15004
Jenison R, Gill S, Polisky B (1995) Oligonucleotide ligands that discriminate between theophylline and caffeine. In: Innis MA, Gelfand DH, Sninsky JJ (eds) PCR Strategies. Academic Press, San Diego, CA, pp 289–299
Chen H, Mcbroom DG, Zhu YQ, Gold L, North TW (1996) Inhibitory RNA ligand to reverse transcriptase from feline immunodeficiency virus. Biochemistry 35:6923–6930
Hermann T, Patel DJ (2000) Adaptive recognition by nucleic acid aptamers. Science 287:820–825
Hicke BJ, Marion C, Chang YF, Gould T, Lynott CK, Parma D, Schmidt PG, Warren S (2001) Tenascin-C aptamers are generated using tumor cells and purified protein. J Biol Chem 276:48644–48654
Da Rocha Gomes S, Miguel J, Azema L, Eimer S, Ries C, Dausse E, Loiseau H, Allard M, Toulmé JJ (2012) (99 m)Tc-MAG3-Aptamer for imaging human tumors associated with high level of Matrix Metalloprotease-9. Bioconjug Chem 23(11):2192–2200
Cho EJ, Lee JW, Ellington AD (2009) Applications of aptamers as sensors. Annu Rev Anal Chem (Palo Alto, Calif) 2:241–264
Mascini M, Palchetti I, Tombelli S (2012) Nucleic acid and peptide aptamers: fundamentals and bioanalytical aspects. Angew Chem Int Ed Engl 51:1316–1332
Lee JH (2013) Conjugation approaches for construction of aptamer-modified nanoparticles for application in imaging. Curr Top Med Chem 13:504–512
Wang AZ, Farokhzad OC (2014) Current progress of aptamer-based molecular imaging. J Nucl Med 55:353–356
Mayer G (2009) The chemical biology of aptamers. Angew Chem Int Ed Engl 48:2672–2689
Hollenstein M (2012) Nucleoside triphosphates–building blocks for the modification of nucleic acids. Molecules 17:13569–13591
Boiziau C, Dausse E, Yurchenko L, Toulmé JJ (1999) DNA aptamers selected against the HIV-1 trans-activation-responsive RNA element form RNA-DNA kissing complexes. J Biol Chem 274:12730–12737
Kikuchi K, Umehara T, Fukuda K, Hwang J, Kuno A, Hasegawa T, Nishikawa S (2003) Structure-inhibition analysis of RNA aptamers that bind to HCV IRES. Nucleic Acids Res Suppl 291–292
Xiao F, Zhang H, Guo P (2008) Novel mechanism of hexamer ring assembly in protein/RNA interactions revealed by single molecule imaging. Nucleic Acids Res 36:6620–6632
Afonin KA, Bindewald E, Yaghoubian AJ, Voss N, Jacovetty E, Shapiro BA, Jaeger L (2010) In vitro assembly of cubic RNA-based scaffolds designed in silico. Nat Nanotechnol 5:676–682
Dausse E, Taouji S, Evadé L, Di Primo C, Chevet E, Toulmé JJ (2011) HAPIscreen, a method for high-throughput aptamer identification. J Nanobiotechnology 9:25
Fukushima N, Weiner JA, Kaushal D, Contos JJ, Rehen SK, Kingsbury MA, Kim KY, Chun J (2002) Lysophosphatidic acid influences the morphology and motility of young, postmitotic cortical neurons. Mol Cell Neurosci 20:271–282
Lee CW, Rivera R, Dubin AE, Chun J (2007) LPA(4)/GPR23 is a lysophosphatidic acid (LPA) receptor utilizing G(s)-, G(q)/G(i)-mediated calcium signaling and G(12/13)-mediated Rho activation. J Biol Chem 282:4310–4317
Platonova N, Miquel G, Regenfuss B, Taouji S, Cursiefen C, Chevet E, Bikfalvi A (2013) Evidence for the interaction of fibroblast growth factor-2 with the lymphatic endothelial cell marker LYVE-1. Blood 121:1229–1237
D’Agostino VG, Adami V, Provenzani A (2013) A novel high throughput biochemical assay to evaluate the HuR protein-RNA complex formation. PLoS One 8:e72426
Gabriel D, Vernier M, Pfeifer MJ, Dasen B, Tenaillon L, Bouhelal R (2003) High throughput screening technologies for direct cyclic AMP measurement. Assay Drug Dev Technol 1:291–303
Gray A, Olsson H, Batty IH, Priganica L, Peter Downes C (2003) Nonradioactive methods for the assay of phosphoinositide 3-kinases and phosphoinositide phosphatases and selective detection of signaling lipids in cell and tissue extracts. Anal Biochem 313:234–245
Cavallini A, Brewerton S, Bell A, Sargent S, Glover S, Hardy C, Moore R, Calley J, Ramachandran D, Poidinger M et al (2013) An unbiased approach to identifying tau kinases that phosphorylate tau at sites associated with Alzheimer disease. J Biol Chem 288:23331–23347
Binder C, Lafayette A, Archibeque I, Sun Y, Plewa C, Sinclair A, Emkey R (2008) Optimization and utilization of the SureFire phospho-STAT5 assay for a cell-based screening campaign. Assay Drug Dev Technol 6:27–37
Dausse E, Cazenave C, Rayner B, Toulmé JJ (2005) In vitro selection procedures for identifying DNA and RNA aptamers targeted to nucleic acids and proteins. Methods Mol Biol 288:391–410
Acknowledgements
We are grateful to Pr D. Desmecht and Dr F. Cornet (University of Liège, Belgium) for help in identification of C1 and C6 aptamers and to T. Crosson for technical assistance.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2015 Springer Science+Business Media New York
About this protocol
Cite this protocol
Evadé, L., Dausse, E., Taouji, S., Daguerre, E., Chevet, E., Toulmé, JJ. (2015). Aptamer-Mediated Nanoparticle Interactions: From Oligonucleotide–Protein Complexes to SELEX Screens. In: Guo, P., Haque, F. (eds) RNA Nanotechnology and Therapeutics. Methods in Molecular Biology, vol 1297. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-2562-9_11
Download citation
DOI: https://doi.org/10.1007/978-1-4939-2562-9_11
Publisher Name: Humana Press, New York, NY
Print ISBN: 978-1-4939-2561-2
Online ISBN: 978-1-4939-2562-9
eBook Packages: Springer Protocols