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DNA-nanostructure-assembly by sequential spotting
BACKGROUND: The ability to create nanostructures with biomolecules is one of the key elements in nanobiotechnology. One of the problems is the expensive and mostly custom made equipment which is needed for their development. We intended to reduce material costs and aimed at miniaturization of the ne...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248840/ https://www.ncbi.nlm.nih.gov/pubmed/22099392 http://dx.doi.org/10.1186/1477-3155-9-54 |
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author | Breitenstein, Michael Nielsen, Peter E Hölzel, Ralph Bier, Frank F |
author_facet | Breitenstein, Michael Nielsen, Peter E Hölzel, Ralph Bier, Frank F |
author_sort | Breitenstein, Michael |
collection | PubMed |
description | BACKGROUND: The ability to create nanostructures with biomolecules is one of the key elements in nanobiotechnology. One of the problems is the expensive and mostly custom made equipment which is needed for their development. We intended to reduce material costs and aimed at miniaturization of the necessary tools that are essential for nanofabrication. Thus we combined the capabilities of molecular ink lithography with DNA-self-assembling capabilities to arrange DNA in an independent array which allows addressing molecules in nanoscale dimensions. RESULTS: For the construction of DNA based nanostructures a method is presented that allows an arrangement of DNA strands in such a way that they can form a grid that only depends on the spotted pattern of the anchor molecules. An atomic force microscope (AFM) has been used for molecular ink lithography to generate small spots. The sequential spotting process allows the immobilization of several different functional biomolecules with a single AFM-tip. This grid which delivers specific addresses for the prepared DNA-strand serves as a two-dimensional anchor to arrange the sequence according to the pattern. Once the DNA-nanoarray has been formed, it can be functionalized by PNA (peptide nucleic acid) to incorporate advanced structures. CONCLUSIONS: The production of DNA-nanoarrays is a promising task for nanobiotechnology. The described method allows convenient and low cost preparation of nanoarrays. PNA can be used for complex functionalization purposes as well as a structural element. |
format | Online Article Text |
id | pubmed-3248840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32488402011-12-31 DNA-nanostructure-assembly by sequential spotting Breitenstein, Michael Nielsen, Peter E Hölzel, Ralph Bier, Frank F J Nanobiotechnology Research BACKGROUND: The ability to create nanostructures with biomolecules is one of the key elements in nanobiotechnology. One of the problems is the expensive and mostly custom made equipment which is needed for their development. We intended to reduce material costs and aimed at miniaturization of the necessary tools that are essential for nanofabrication. Thus we combined the capabilities of molecular ink lithography with DNA-self-assembling capabilities to arrange DNA in an independent array which allows addressing molecules in nanoscale dimensions. RESULTS: For the construction of DNA based nanostructures a method is presented that allows an arrangement of DNA strands in such a way that they can form a grid that only depends on the spotted pattern of the anchor molecules. An atomic force microscope (AFM) has been used for molecular ink lithography to generate small spots. The sequential spotting process allows the immobilization of several different functional biomolecules with a single AFM-tip. This grid which delivers specific addresses for the prepared DNA-strand serves as a two-dimensional anchor to arrange the sequence according to the pattern. Once the DNA-nanoarray has been formed, it can be functionalized by PNA (peptide nucleic acid) to incorporate advanced structures. CONCLUSIONS: The production of DNA-nanoarrays is a promising task for nanobiotechnology. The described method allows convenient and low cost preparation of nanoarrays. PNA can be used for complex functionalization purposes as well as a structural element. BioMed Central 2011-11-18 /pmc/articles/PMC3248840/ /pubmed/22099392 http://dx.doi.org/10.1186/1477-3155-9-54 Text en Copyright ©2011 Breitenstein et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Breitenstein, Michael Nielsen, Peter E Hölzel, Ralph Bier, Frank F DNA-nanostructure-assembly by sequential spotting |
title | DNA-nanostructure-assembly by sequential spotting |
title_full | DNA-nanostructure-assembly by sequential spotting |
title_fullStr | DNA-nanostructure-assembly by sequential spotting |
title_full_unstemmed | DNA-nanostructure-assembly by sequential spotting |
title_short | DNA-nanostructure-assembly by sequential spotting |
title_sort | dna-nanostructure-assembly by sequential spotting |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248840/ https://www.ncbi.nlm.nih.gov/pubmed/22099392 http://dx.doi.org/10.1186/1477-3155-9-54 |
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