Different approaches for the detection of thrombin by an electrochemical aptamer-based assay coupled to magnetic beads

• Published in: Biosensors & bioelectronics Vol. 23; no. 11; pp. 1602 - 1609
• Main Authors: Centi, S., Messina, G., Tombelli, S., Palchetti, I., Mascini, M.
• Format: Journal Article
• Language: English
• Published: Lausanne Elsevier B.V 15-06-2008; Elsevier Science
• Subjects: Aptamer; Aptamers, Nucleotide - chemistry; Biological and medical sciences; Biosensing Techniques - instrumentation; Biotechnology; Electrochemical detection; Electrochemistry - instrumentation; Electrochemistry - methods; Equipment Design; Equipment Failure Analysis; Fundamental and applied biological sciences. Psychology; Immunomagnetic Separation - instrumentation; Immunomagnetic Separation - methods; Magnetic beads; Methods. Procedures. Technologies; Microspheres; Others; Thrombin; Thrombin - analysis; Thrombin - chemistry; Various methods and equipments; Magnetic beads; Thrombin; Aptamer; Electrochemical detection; Peptidases; Serine endopeptidases; Enzyme; Electrochemistry; Hydrolases; Method; Detection
• ISSN: 0956-5663; 1873-4235
• DOI: 10.1016/j.bios.2008.01.020

Different assay formats based on the coupling of magnetic beads with electrochemical transduction were compared here for the detection of thrombin by using a thrombin specific aptamer. By using the thrombin-binding aptamer, a direct and an indirect competitive assay for thrombin have been developed by immobilising the aptamer or the protein, respectively. Moreover, another strategy was based on the direct measurement of the enzymatic product of thrombin captured by the immobilised aptamer. All the assays were developed by coupling the electrochemical transduction with the innovative and advantageous use of magnetic beads.
The assays based on the immobilisation of the protein were not successful since no binding was recorded between thrombin and its aptamer. With the direct competitive assay, when the aptamer was immobilised onto the magnetic beads, a detection limit of 430
nM for thrombin was achieved. A lower detection limit for the protein (175
nM) was instead obtained by detecting the product of the enzymatic reaction catalysed by thrombin. All these assays were finally compared with a sandwich assay which reached a detection limit of 0.45
nM of thrombin demonstrating the best analytical performances.
With this comparison the importance of a deep study on the different analytical approaches for thrombin detection to reach the performances of the best assay configuration has been demonstrated.