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Gold Nanoparticles Used as Protein Scavengers Enhance Surface Plasmon Resonance Signal.
Ferreira de Macedo, Erenildo; Ducatti Formaggio, Daniela Maria; Salles Santos, Nivia; Batista Tada, Dayane.
Affiliation
  • Ferreira de Macedo E; Instituto de Ciência e Tecnologia, Universidade Federal de São Paulo, Rua Talim 330, Vila Nair, São José dos Campos, SP 12231-280, Brazil. e.macedo@unifesp.br.
  • Ducatti Formaggio DM; Instituto de Ciência e Tecnologia, Universidade Federal de São Paulo, Rua Talim 330, Vila Nair, São José dos Campos, SP 12231-280, Brazil. dformaggio@unifesp.br.
  • Salles Santos N; Instituto de Ciência e Tecnologia, Universidade Federal de São Paulo, Rua Talim 330, Vila Nair, São José dos Campos, SP 12231-280, Brazil. nivia.salles@unifesp.br.
  • Batista Tada D; Instituto de Ciência e Tecnologia, Universidade Federal de São Paulo, Rua Talim 330, Vila Nair, São José dos Campos, SP 12231-280, Brazil. d.tada@unifesp.br.
Sensors (Basel) ; 17(12)2017 Nov 29.
Article in En | MEDLINE | ID: mdl-29186024
Although several researchers had reported on methodologies for surface plasmon resonance (SPR) signal amplification based on the use of nanoparticles (NPs), the majority addressed the sandwich technique and low protein concentration. In this work, a different approach for SPR signal enhancement based on the use of gold NPs was evaluated. The method was used in the detection of two lectins, peanut agglutinin (PNA) and concanavalin A (ConA). Gold NPs were functionalized with antibodies anti-PNA and anti-ConA, and these NPs were used as protein scavengers in a solution. After being incubated with solutions of PNA or ConA, the gold NPs coupled with the collected lectins were injected on the sensor containing the immobilized antibodies. The signal amplification provided by this method was compared to the signal amplification provided by the direct coupling of PNA and ConA to gold NPs. Furthermore, both methods, direct coupling and gold NPs as protein scavengers, were compared to the direct detection of PNA and ConA in solution. Compared to the analysis of free protein, the direct coupling of PNA and ConA to gold NPs resulted in a signal amplification of 10-40-fold and a 13-fold decrease of the limit of detection (LOD), whereas the use of gold NPs as protein scavengers resulted in an SPR signal 40-50-times higher and an LOD 64-times lower.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Sensors (Basel) Year: 2017 Document type: Article Affiliation country: Brazil Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Sensors (Basel) Year: 2017 Document type: Article Affiliation country: Brazil Country of publication: Switzerland