Studies of Listeria monocytogenes–antibody binding using electro-orientation

An electro-optical (EO) approach has been used for studies of Listeria monocytogenes–antibody binding. The EO analyzer, which has been developed at the State Research Center for Applied Microbiology, Obolensk, was used as a basic instrument for EO measurements. AC electro-kinetic effects depend on d...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biosensors & bioelectronics 2004-07, Vol.19 (12), p.1759-1761
Hauptverfasser: Bunin, Victor D, Ignatov, Oleg V, Guliy, Olga I, Voloshin, Alexandr G, Dykman, Lev A, O’Neil, Daniel, Ivnitski, Dmitri
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:An electro-optical (EO) approach has been used for studies of Listeria monocytogenes–antibody binding. The EO analyzer, which has been developed at the State Research Center for Applied Microbiology, Obolensk, was used as a basic instrument for EO measurements. AC electro-kinetic effects depend on dielectric properties of bioparticles, their composition, morphology, the medium, and the frequency of applied electrical field. Electro-orientational spectra were used for discrimination of bacteria before and after selective binding with antibodies. The measurements were performed using a discrete set of frequencies of the orienting electric field (10, 100, 250, and 500 kHz). During biospecific interactions an antibody is bound to the microorganism causing a change in the dielectric properties of the microorganism–antibody complex and the EO signal reaches its maximum at 100–200 kHz. It has been shown that the biospecific interactions of L. monocytogenes cells with anti- Listeria antibody in the presence of Escherichia coli K-12, and Azospirillum brasilense Sp7 change the EO signals significantly. Thus, the determination of the presence of particular bacteria within a mixed sample may be achieved by selection and matching of antibodies specific to individual bacterium types and by comparing spectra of bacterium in the presence and in the absence of specific antibody.
ISSN:0956-5663
1873-4235
DOI:10.1016/j.bios.2003.12.027