Site-selective immobilization of gold nanoparticles functionalized with DNA oligomers |
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Authors: | C M Niemeyer B Ceyhan S Gao L Chi S Peschel U Simon |
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Institution: | Universit?t Bremen, FB2 – UFT Biotechnologie und Molekulare Genetik Leobener Str., 28359 Bremen, Germany e-mail: cmn@biotec.uni-bremen.de Fax: + 49 (0421 218 7578), DE Physikalisches Institut der Universit?t Münster, Wilhelm-Klemm Str. 10 48149 Münster, Germany, DE Institut für Anorganische Chemie der RWTH Aachen, Prof.-Pirlet-Str. 1 52056 Aachen, Germany, DE
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Abstract: | The organization of metal and semiconductor nanoparticles to form micro- and nanostructured assemblies is currently of tremendous
interest. This communication reports on the utilization of DNA molecules as positioning elements for generating microstructured
surface architecture from gold nanoparticles. Citrate-passivated 40 nm gold colloids were modified by chemisorptive coupling
with a 5′-thiol-derivatized DNA oligomer. The nucleic acid was used as a molecular handle for the specific immobilization
on solid supports, previously functionalized with capture DNA oligomers, complementary to the nanoparticle-bound DNA. As a
consequence of the enormous specificity of nucleic acid hybridization, the DNA-directed immobilization (DDI) allows, to site-specifically
target the hybrid nanoparticles to microlocations which contain the complementary oligomers. The site-selectivity of the surface
adsorption is demonstrated by immobilizing the gold colloids on a DNA microarray on a glass cover slide. Moreover, scanning
force microscopy (SFM) analysis, used to characterize the intermediate steps of the DDI on a gold substrate, provided initial
insights into the specificity and efficiency of this technique. The application of the DDI to fabricate complex colloidal
micro- and nanostructures is anticipated.
Received: 26 July 2000/Accepted: 5 October 2000 |
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Keywords: | Gold nanoparticles Nucleic acids Nanostructures Surface architecture Self-assembly |
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