Cargando…
DNA Nanoparticles for Improved Protein Synthesis In Vitro
The amplification and digital quantification of single DNA molecules are important in biomedicine and diagnostics. Beyond quantifying DNA molecules in a sample, the ability to express proteins from the amplified DNA would open even broader applications in synthetic biology, directed evolution, and p...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787208/ https://www.ncbi.nlm.nih.gov/pubmed/26821778 http://dx.doi.org/10.1002/anie.201511809 |
_version_ | 1782420664667340800 |
---|---|
author | Galinis, Robertas Stonyte, Greta Kiseliovas, Vaidotas Zilionis, Rapolas Studer, Sabine Hilvert, Donald Janulaitis, Arvydas Mazutis, Linas |
author_facet | Galinis, Robertas Stonyte, Greta Kiseliovas, Vaidotas Zilionis, Rapolas Studer, Sabine Hilvert, Donald Janulaitis, Arvydas Mazutis, Linas |
author_sort | Galinis, Robertas |
collection | PubMed |
description | The amplification and digital quantification of single DNA molecules are important in biomedicine and diagnostics. Beyond quantifying DNA molecules in a sample, the ability to express proteins from the amplified DNA would open even broader applications in synthetic biology, directed evolution, and proteomics. Herein, a microfluidic approach is reported for the production of condensed DNA nanoparticles that can serve as efficient templates for in vitro protein synthesis. Using phi29 DNA polymerase and a multiple displacement amplification reaction, single DNA molecules were converted into DNA nanoparticles containing up to about 10(4) clonal gene copies of the starting template. DNA nanoparticle formation was triggered by accumulation of inorganic pyrophosphate (produced during DNA synthesis) and magnesium ions from the buffer. Transcription–translation reactions performed in vitro showed that individual DNA nanoparticles can serve as efficient templates for protein synthesis in vitro. |
format | Online Article Text |
id | pubmed-4787208 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-47872082016-04-08 DNA Nanoparticles for Improved Protein Synthesis In Vitro Galinis, Robertas Stonyte, Greta Kiseliovas, Vaidotas Zilionis, Rapolas Studer, Sabine Hilvert, Donald Janulaitis, Arvydas Mazutis, Linas Angew Chem Int Ed Engl Communications The amplification and digital quantification of single DNA molecules are important in biomedicine and diagnostics. Beyond quantifying DNA molecules in a sample, the ability to express proteins from the amplified DNA would open even broader applications in synthetic biology, directed evolution, and proteomics. Herein, a microfluidic approach is reported for the production of condensed DNA nanoparticles that can serve as efficient templates for in vitro protein synthesis. Using phi29 DNA polymerase and a multiple displacement amplification reaction, single DNA molecules were converted into DNA nanoparticles containing up to about 10(4) clonal gene copies of the starting template. DNA nanoparticle formation was triggered by accumulation of inorganic pyrophosphate (produced during DNA synthesis) and magnesium ions from the buffer. Transcription–translation reactions performed in vitro showed that individual DNA nanoparticles can serve as efficient templates for protein synthesis in vitro. John Wiley and Sons Inc. 2016-01-28 2016-02 /pmc/articles/PMC4787208/ /pubmed/26821778 http://dx.doi.org/10.1002/anie.201511809 Text en CC-BY-NC-ND © 2016 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Communications Galinis, Robertas Stonyte, Greta Kiseliovas, Vaidotas Zilionis, Rapolas Studer, Sabine Hilvert, Donald Janulaitis, Arvydas Mazutis, Linas DNA Nanoparticles for Improved Protein Synthesis In Vitro |
title | DNA Nanoparticles for Improved Protein Synthesis In Vitro |
title_full | DNA Nanoparticles for Improved Protein Synthesis In Vitro |
title_fullStr | DNA Nanoparticles for Improved Protein Synthesis In Vitro |
title_full_unstemmed | DNA Nanoparticles for Improved Protein Synthesis In Vitro |
title_short | DNA Nanoparticles for Improved Protein Synthesis In Vitro |
title_sort | dna nanoparticles for improved protein synthesis in vitro |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787208/ https://www.ncbi.nlm.nih.gov/pubmed/26821778 http://dx.doi.org/10.1002/anie.201511809 |
work_keys_str_mv | AT galinisrobertas dnananoparticlesforimprovedproteinsynthesisinvitro AT stonytegreta dnananoparticlesforimprovedproteinsynthesisinvitro AT kiseliovasvaidotas dnananoparticlesforimprovedproteinsynthesisinvitro AT zilionisrapolas dnananoparticlesforimprovedproteinsynthesisinvitro AT studersabine dnananoparticlesforimprovedproteinsynthesisinvitro AT hilvertdonald dnananoparticlesforimprovedproteinsynthesisinvitro AT janulaitisarvydas dnananoparticlesforimprovedproteinsynthesisinvitro AT mazutislinas dnananoparticlesforimprovedproteinsynthesisinvitro |