Preferential attachment of specific fluorescent dyes and dye labeled dna sequences in a surface enhanced raman scattering multiplex
Gracie, Kirsten and Moores, Matthew and Smith, W. Ewen and Harding, Kerry and Girolami, Mark and Graham, Duncan and Faulds, Karen (2016) Preferential attachment of specific fluorescent dyes and dye labeled dna sequences in a surface enhanced raman scattering multiplex. Analytical Chemistry, 88 (2). pp. 1147-1153. ISSN 0003-2700 (https://doi.org/10.1021/acs.analchem.5b02776)
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Abstract
A significant advantage of using surface enhanced Raman scattering (SERS) for DNA detection is the capability to detect multiple analytes simultaneously within the one sample. However, as the analytes approach the metallic surface required for SERS, they become more concentrated and previous studies have suggested that different dye labels will have different affinities for the metal surface. Here, the interaction of single stranded DNA labeled with either fluorescein (FAM) or tetramethylrhodamine (TAMRA) with a metal surface, using spermine induced aggregated silver nanoparticles as the SERS substrate, is investigated by analyzing the labels separately and in mixtures. Comparison studies were also undertaken using the dyes in their free isothiocyanate forms, fluorescein isothiocyanate (F-ITC) and tetramethylrhodamine isothiocyanate (TR-ITC). When the two dyes are premixed prior to the addition of nanoparticles, TAMRA exerts a strong masking effect over FAM due to a stronger affinity for the metal surface. When parameters such as order of analyte addition, analysis time, and analyte concentration are investigated, the masking effect of TAMRA is still observed but the extent changes depending on the experimental parameters. By using bootstrap estimation of changes in SERS peak intensity, a greater insight has been achieved into the surface affinity of the two dyes as well as how they interact with each other. It has been shown that the order of addition of the analytes is important and that specific dye related interactions occur, which could greatly affect the observed SERS spectra. SERS has been used successfully for the simultaneous detection of several analytes; however, this work has highlighted the significant factors that must be taken into consideration when planning a multiple analyte assay.
ORCID iDs
Gracie, Kirsten ORCID: https://orcid.org/0000-0003-3149-3357, Moores, Matthew, Smith, W. Ewen, Harding, Kerry, Girolami, Mark, Graham, Duncan ORCID: https://orcid.org/0000-0002-6079-2105 and Faulds, Karen ORCID: https://orcid.org/0000-0002-5567-7399;-
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Item type: Article ID code: 56035 Dates: DateEvent19 January 2016Published23 December 2015Published Online23 December 2015AcceptedSubjects: Science > Chemistry Department: University of Strathclyde > University of Strathclyde
Faculty of Science > Pure and Applied Chemistry
Technology and Innovation Centre > BionanotechnologyDepositing user: Pure Administrator Date deposited: 30 Mar 2016 14:39 Last modified: 11 Nov 2024 11:19 Related URLs: URI: https://strathprints.strath.ac.uk/id/eprint/56035