Biospecific Interaction Analysis in Real Time Using a Biosensor System with Surface Plasmon Resonance Detection

1994 ◽  
pp. 113-129
Author(s):  
Lars G. Fägerstam
1992 ◽  
Vol 597 (1-2) ◽  
pp. 397-410 ◽  
Author(s):  
Lars G. Fägerstam ◽  
Åsa Frostell-Karlsson ◽  
Robert Karlsson ◽  
Björn Persson ◽  
Inger Rönnberg

2010 ◽  
Vol 26 (4) ◽  
pp. 1554-1559 ◽  
Author(s):  
Marie-Bernadette Villiers ◽  
Sandra Cortès ◽  
Carine Brakha ◽  
Jean-Pierre Lavergne ◽  
Christophe A. Marquette ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-19 ◽  
Author(s):  
Markus Ritzefeld ◽  
Norbert Sewald

Several proteins, like transcription factors, bind to certain DNA sequences, thereby regulating biochemical pathways that determine the fate of the corresponding cell. Due to these key positions, it is indispensable to analyze protein-DNA interactions and to identify their mode of action. Surface plasmon resonance is a label-free method that facilitates the elucidation of real-time kinetics of biomolecular interactions. In this article, we focus on this biosensor-based method and provide a detailed guide how SPR can be utilized to study binding of proteins to oligonucleotides. After a description of the physical phenomenon and the instrumental realization including fiber-optic-based SPR and SPR imaging, we will continue with a survey of immobilization methods. Subsequently, we will focus on the optimization of the experiment, expose pitfalls, and introduce how data should be analyzed and published. Finally, we summarize several interesting publications of the last decades dealing with protein-DNA and RNA interaction analysis by SPR.


2006 ◽  
Vol 89 (3) ◽  
pp. 893-897 ◽  
Author(s):  
Roberto Gambari ◽  
Giordana Feriotto

Abstract A review is presented demonstrating that biospecific interaction analysis, using surface plasmon resonance (SPR) and biosensor technologies is a simple, rapid, and automatable approach to detect genetically modified organisms (GMOs). Using SPR, we were able to monitor in real-time the hybridization between oligonucleotide or polymerase chain reaction (PCR)-generated probes and target single-stranded PCR products obtained by using as substrates DNA isolated from normal or transgenic soybean and maize. This procedure allows a one-step, nonradioactive detection of GMOs. PCR-generated probes are far more efficient in detecting GMOs than are oligodeoxyribonucleotide probes. This is expected to be a very important parameter, because information on low percentage of GMOs is of great value. Determination of the ability of SPR-based analysis to quantify GMOs should be considered a major research field for future studies, especially for the analyses of food supplies.


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