alexa Immobilization of P22 Bacteriophage Tailspike Protein on Si Surface for Optimized Salmonella Capture | OMICS International | Abstract
ISSN: 2155-9872

Journal of Analytical & Bioanalytical Techniques
Open Access

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Research Article

Immobilization of P22 Bacteriophage Tailspike Protein on Si Surface for Optimized Salmonella Capture

Sarang Dutt1,2, Jamshid Tanha3 , Stephane Evoy1,2, and Amit Singh1,2,4*

1Electrical and Computer Engineering, University of Alberta, Canada

2National Institute for Nanotechnology, University of Alberta, Canada

3Human Health Therapeutics, National Research Council Canada, Canada

4Department of Pharmaceutical Sciences, Northeastern University, USA

*Corresponding Author:
Amit Singh
Department of Pharmaceutical Sciences
Northeastern University
Boston, MA, 02176 USA
Tel: +1 617 373 3127
E-mail: [email protected]

Received date: February 27, 2013; Accepted date: April 22, 2013; Published date: April 24, 2013

Citation: Dutt S, Tanha J, Evoy S, Singh A (2013) Immobilization of P22 Bacteriophage Tailspike Protein on Si Surface for Optimized Salmonella Capture. J Anal Bioanal Techniques S7:007. doi: 10.4172/2155-9872.S7-007

Copyright: © 2013 Dutt S, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Bacteriophage based technology has gained interest in developing pathogen detection platforms for biosensing applications. In this study, P22 phage tail spike proteins (TSPs) have been immobilized on Si surfaces for optimized capture of host Salmonella enteric serovar Typhimurium. It was then demonstrated that roughening of the Si surface before the TSP immobilization improves the bacterial capture 2-fold compared to a flat Si surface. Coarse, medium, fine and superfine size ridges were patterned on the Si surface using block copolymer layer and plasma etching and each surface was functionalized by TSPs for bacterial capture. The capture density increased with decreasing size of the ridge until it reached an optimum for fine ridges; the capture density decreased when the surface ridges were superfine and deep. This method shows a 22-fold and 3-fold increase in bacterial capture density compared to a Cys- and a His6-tag based oriented TSP immobilization, respectively. Bovine serum albumin (BSA) was used as a surface protective layer to prevent non-specific binding of bacteria and E. coli cells were used as control to demonstrate the specificity of recognition. Negligible binding was observed for control bacteria in presence of TSPs and the host bacteria in the absence of TSP on the surfaces.

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