Development of bionanotechnological strategies for signal enhancement in nucleic acids biosensors

Nucleic acid biosensors represent a powerful tool for clinical and environmental pathogens detection. For applications such as point-of-care biosensing, it is fundamental to develop sensors that should be automatic, inexpensive, portable and require a professional skill of the user that should be as...

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Main Author: Vinelli, Alessandra <1982>
Other Authors: Samorì, Bruno
Format: Doctoral Thesis
Language:en
Published: Alma Mater Studiorum - Università di Bologna 2011
Subjects:
Online Access:http://amsdottorato.unibo.it/3751/
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spelling ndltd-unibo.it-oai-amsdottorato.cib.unibo.it-37512014-03-24T16:29:20Z Development of bionanotechnological strategies for signal enhancement in nucleic acids biosensors Vinelli, Alessandra <1982> CHIM/06 Chimica organica Nucleic acid biosensors represent a powerful tool for clinical and environmental pathogens detection. For applications such as point-of-care biosensing, it is fundamental to develop sensors that should be automatic, inexpensive, portable and require a professional skill of the user that should be as low as possible. With the goal of determining the presence of pathogens when present in very small amount, such as for the screening of pathogens in drinking water, an amplification step must be implemented. Often this type of determinations should be performed with simple, automatic and inexpensive hardware: the use of a chemical (or nanotechnological) isothermal solution would be desirable. My Ph.D. project focused on the study and on the testing of four isothermal reactions which can be used to amplify the nucleic acid analyte before the binding event on the surface sensor or to amplify the signal after that the hybridization event with the probe. Recombinase polymerase amplification (RPA) and ligation-mediated rolling circle amplification (L-RCA) were investigated as methods for DNA and RNA amplification. Hybridization chain reaction (HCR) and Terminal deoxynucleotidil transferase-mediated amplification were investigated as strategies to achieve the enhancement of the signal after the surface hybridization event between target and probe. In conclusion, it can be said that only a small subset of the biochemical strategies that are proved to work in solution towards the amplification of nucleic acids does truly work in the context of amplifying the signal of a detection system for pathogens. Amongst those tested during my Ph.D. activity, recombinase polymerase amplification seems the best candidate for a useful implementation in diagnostic or environmental applications. Alma Mater Studiorum - Università di Bologna Samorì, Bruno 2011-04-15 Doctoral Thesis PeerReviewed application/pdf en http://amsdottorato.unibo.it/3751/ info:eu-repo/semantics/openAccess
collection NDLTD
language en
format Doctoral Thesis
sources NDLTD
topic CHIM/06 Chimica organica
spellingShingle CHIM/06 Chimica organica
Vinelli, Alessandra <1982>
Development of bionanotechnological strategies for signal enhancement in nucleic acids biosensors
description Nucleic acid biosensors represent a powerful tool for clinical and environmental pathogens detection. For applications such as point-of-care biosensing, it is fundamental to develop sensors that should be automatic, inexpensive, portable and require a professional skill of the user that should be as low as possible. With the goal of determining the presence of pathogens when present in very small amount, such as for the screening of pathogens in drinking water, an amplification step must be implemented. Often this type of determinations should be performed with simple, automatic and inexpensive hardware: the use of a chemical (or nanotechnological) isothermal solution would be desirable. My Ph.D. project focused on the study and on the testing of four isothermal reactions which can be used to amplify the nucleic acid analyte before the binding event on the surface sensor or to amplify the signal after that the hybridization event with the probe. Recombinase polymerase amplification (RPA) and ligation-mediated rolling circle amplification (L-RCA) were investigated as methods for DNA and RNA amplification. Hybridization chain reaction (HCR) and Terminal deoxynucleotidil transferase-mediated amplification were investigated as strategies to achieve the enhancement of the signal after the surface hybridization event between target and probe. In conclusion, it can be said that only a small subset of the biochemical strategies that are proved to work in solution towards the amplification of nucleic acids does truly work in the context of amplifying the signal of a detection system for pathogens. Amongst those tested during my Ph.D. activity, recombinase polymerase amplification seems the best candidate for a useful implementation in diagnostic or environmental applications.
author2 Samorì, Bruno
author_facet Samorì, Bruno
Vinelli, Alessandra <1982>
author Vinelli, Alessandra <1982>
author_sort Vinelli, Alessandra <1982>
title Development of bionanotechnological strategies for signal enhancement in nucleic acids biosensors
title_short Development of bionanotechnological strategies for signal enhancement in nucleic acids biosensors
title_full Development of bionanotechnological strategies for signal enhancement in nucleic acids biosensors
title_fullStr Development of bionanotechnological strategies for signal enhancement in nucleic acids biosensors
title_full_unstemmed Development of bionanotechnological strategies for signal enhancement in nucleic acids biosensors
title_sort development of bionanotechnological strategies for signal enhancement in nucleic acids biosensors
publisher Alma Mater Studiorum - Università di Bologna
publishDate 2011
url http://amsdottorato.unibo.it/3751/
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