Raman Mapping of Biological Systems Interacting with a Disordered Nanostructured Surface: A Simple and Powerful Approach to the Label-Free Analysis of Single DNA Bases.

principal component analysis raman mapping silicon nanowires single DNA bases

Journal

Micromachines
ISSN: 2072-666X
Titre abrégé: Micromachines (Basel)
Pays: Switzerland
ID NLM: 101640903

Informations de publication

Date de publication:
04 Mar 2021
Historique:
received: 19 02 2021
revised: 27 02 2021
accepted: 01 03 2021
entrez: 3 4 2021
pubmed: 4 4 2021
medline: 4 4 2021
Statut: epublish

Résumé

This article demonstrates the possibility to use a novel powerful approach based on Raman mapping of analyte solutions drop casted on a disordered array of Ag covered silicon nanowires (Ag/SiNWs), to identify the characteristic spectral signal of the four DNA bases, adenine (A), thymine (T), cytosine (C), and guanine (G), at concentration as low as 10 ng/µL, and to study their specific way of interacting with the nanostructured substrate. The results show a distinctive and amplified interaction of guanine, the base that is most susceptible to oxidation, with the nanostructured surface. Our findings explain the recently revealed diverse behaviour of cancer and normal DNA deposited on the same Ag/SiNWs, which is ascribed to mechanical deformation and base lesions present on the oxidised DNA molecule backbone and causes detectable variation in the Raman signal, usable for diagnostic purposes. The notable bio-analytical capability of the presented platform, and its sensitivity to the molecule mechanical conformation at the single-base level, thus provides a new reliable, rapid, label-free DNA diagnostic methodology alternative to more sophisticated and expensive sequencing ones.

Identifiants

pubmed: 33806524
pii: mi12030264
doi: 10.3390/mi12030264
pmc: PMC8000830
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Italian Minister of Foreign Affairs and International Collaboration (MAECI)
ID : US19GR07

Références

Adv Healthc Mater. 2016 Mar 9;5(5):575-83
pubmed: 26717420
J Am Chem Soc. 2006 Dec 20;128(50):16323-31
pubmed: 17165787
Hum Genomics. 2019 Aug 1;13(1):34
pubmed: 31370908
Ann Oncol. 2017 Mar 1;28(3):468-477
pubmed: 27998963
Anal Chem. 2007 May 1;79(9):3291-7
pubmed: 17407259
ACS Nano. 2020 Mar 24;14(3):2585-2627
pubmed: 32031781
Sci Rep. 2016 Apr 26;6:25099
pubmed: 27112197
Nano Lett. 2008 Apr;8(4):1066-70
pubmed: 18311939
J Phys Chem C Nanomater Interfaces. 2016 Jul 21;120(28):15415-15423
pubmed: 28077982
Methods Enzymol. 1987;155:335-50
pubmed: 3431465
J Am Chem Soc. 2007 Jun 13;129(23):7228-9
pubmed: 17516647
J Am Chem Soc. 2013 Mar 27;135(12):4815-21
pubmed: 23470053
Nat Methods. 2008 Jan;5(1):16-8
pubmed: 18165802
Adv Mater. 2012 Mar 8;24(10):OP11-8
pubmed: 22105972
Mater Sci Eng C Mater Biol Appl. 2021 Mar;122:111951
pubmed: 33641882
APMIS. 2004 Nov-Dec;112(11-12):808-14
pubmed: 15688523
Cancer Discov. 2016 May;6(5):479-91
pubmed: 26969689
ACS Sens. 2018 Sep 28;3(9):1690-1697
pubmed: 30132653
Adv Healthc Mater. 2021 Feb;10(3):e2001110
pubmed: 33236490
Nanotechnology. 2018 Oct 12;29(41):415102
pubmed: 30059014
Nat Commun. 2019 Nov 22;10(1):5321
pubmed: 31757965
ACS Appl Mater Interfaces. 2009 Jul;1(7):1396-403
pubmed: 20355941

Auteurs

Valentina Mussi (V)

Institute for Microelectronics and Microsystems, National Research Council, IMM-CNR, 00133 Rome, Italy.

Mario Ledda (M)

Institute of Translational Pharmacology, National Research Council, IFT-CNR, 00133 Rome, Italy.

Annalisa Convertino (A)

Institute for Microelectronics and Microsystems, National Research Council, IMM-CNR, 00133 Rome, Italy.

Antonella Lisi (A)

Institute of Translational Pharmacology, National Research Council, IFT-CNR, 00133 Rome, Italy.

Classifications MeSH