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Development of rolling circle amplification based surface-enhanced Raman spectroscopy method for 35S promoter gene detection.
Talanta. 2015 May; 136:68-74.T

Abstract

In this study, we developed the genetically modified organism detection method by using the combination of rolling circle amplification (RCA) and surface-enhanced Raman spectroscopy (SERS). An oligonucleotide probe which is specific for 35S DNA promoter target was immobilised onto the gold slide and a RCA reaction was performed. A self-assembled monolayer was formed on gold nanorods using 5,5'-dithiobis(2-nitrobenzoic acid) (DTNB) and the second probe of the 35S DNA promoter target was immobilised on the activated gold coated slide surfaces. Probes on the nanoparticles were hybridised with the target oligonucleotide. Quantification of the target concentration was performed via SERS spectra of DTNB on the nanorods. SERS spectra of target molecules were enhanced through the RCA reaction and the detection limit was found to be 6.3fM. The sensitivity of the developed RCA-SERS method was compared with another method which had been performed without using RCA reaction, and the detection limit was found to be 0.1pM. The correlation between the target concentration and the SERS signal was found to be linear, within the range of 1pM to 10nM for the traditional assay and 100fM to 100nM for the RCA assay. For the developed RCA-SERS assay, the specificity tests were performed using the 35S promoter of Bt-176 maize gene. It was found out that the developed RCA-SERS sandwich assay method is quite sensitive, selective and specific for target sequences in model and real systems.

Authors+Show Affiliations

Department of Food Engineering, Faculty of Engineering, Hacettepe University, Beytepe, Ankara 06800, Turkey.Department of Food Engineering, Faculty of Engineering, Hacettepe University, Beytepe, Ankara 06800, Turkey; Food Research Center, Hacettepe University, Beytepe, Ankara 06800, Turkey. Electronic address: ihb@hacettepe.edu.tr.Department of Analytical Chemistry, Faculty of Pharmacy, Gazi University, Ankara 06330, Turkey.Food Research Center, Hacettepe University, Beytepe, Ankara 06800, Turkey.Department of Analytical Chemistry, Faculty of Pharmacy, Gazi University, Ankara 06330, Turkey.

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

25702987

Citation

Guven, Burcu, et al. "Development of Rolling Circle Amplification Based Surface-enhanced Raman Spectroscopy Method for 35S Promoter Gene Detection." Talanta, vol. 136, 2015, pp. 68-74.
Guven B, Boyaci IH, Tamer U, et al. Development of rolling circle amplification based surface-enhanced Raman spectroscopy method for 35S promoter gene detection. Talanta. 2015;136:68-74.
Guven, B., Boyaci, I. H., Tamer, U., Acar-Soykut, E., & Dogan, U. (2015). Development of rolling circle amplification based surface-enhanced Raman spectroscopy method for 35S promoter gene detection. Talanta, 136, 68-74. https://doi.org/10.1016/j.talanta.2014.11.051
Guven B, et al. Development of Rolling Circle Amplification Based Surface-enhanced Raman Spectroscopy Method for 35S Promoter Gene Detection. Talanta. 2015;136:68-74. PubMed PMID: 25702987.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Development of rolling circle amplification based surface-enhanced Raman spectroscopy method for 35S promoter gene detection. AU - Guven,Burcu, AU - Boyaci,Ismail Hakki, AU - Tamer,Ugur, AU - Acar-Soykut,Esra, AU - Dogan,Uzeyir, Y1 - 2015/01/12/ PY - 2014/09/17/received PY - 2014/11/14/revised PY - 2014/11/22/accepted PY - 2015/2/24/entrez PY - 2015/2/24/pubmed PY - 2015/12/15/medline KW - DTNB KW - SERS KW - Traditional and RCA sandwich assay SP - 68 EP - 74 JF - Talanta JO - Talanta VL - 136 N2 - In this study, we developed the genetically modified organism detection method by using the combination of rolling circle amplification (RCA) and surface-enhanced Raman spectroscopy (SERS). An oligonucleotide probe which is specific for 35S DNA promoter target was immobilised onto the gold slide and a RCA reaction was performed. A self-assembled monolayer was formed on gold nanorods using 5,5'-dithiobis(2-nitrobenzoic acid) (DTNB) and the second probe of the 35S DNA promoter target was immobilised on the activated gold coated slide surfaces. Probes on the nanoparticles were hybridised with the target oligonucleotide. Quantification of the target concentration was performed via SERS spectra of DTNB on the nanorods. SERS spectra of target molecules were enhanced through the RCA reaction and the detection limit was found to be 6.3fM. The sensitivity of the developed RCA-SERS method was compared with another method which had been performed without using RCA reaction, and the detection limit was found to be 0.1pM. The correlation between the target concentration and the SERS signal was found to be linear, within the range of 1pM to 10nM for the traditional assay and 100fM to 100nM for the RCA assay. For the developed RCA-SERS assay, the specificity tests were performed using the 35S promoter of Bt-176 maize gene. It was found out that the developed RCA-SERS sandwich assay method is quite sensitive, selective and specific for target sequences in model and real systems. SN - 1873-3573 UR - https://www.unboundmedicine.com/medline/citation/25702987/Development_of_rolling_circle_amplification_based_surface_enhanced_Raman_spectroscopy_method_for_35S_promoter_gene_detection_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0039-9140(14)00962-X DB - PRIME DP - Unbound Medicine ER -