4.7 Article

Development and In-Depth Characterization of Bacteria Repellent and Bacteria Adhesive Antibody-Coated Surfaces Using Optical Waveguide Biosensing

期刊

BIOSENSORS-BASEL
卷 12, 期 2, 页码 -

出版社

MDPI
DOI: 10.3390/bios12020056

关键词

bacteria sensing; bacteria repellent coatings; affinity layers; layer structure; binding kinetics; Escherichia coli; ELISA; BSA; I-block; PLL-g-PEG; PAcrAM-g-(PMOXA; NH2; Si); polyclonal and monoclonal antibodies (Abs); antibody orientation; OWLS; waveguide sensing; physisorption; Avidin-biotin; AnteoBind; protein A

资金

  1. Hungarian Academy of Sciences (Lendulet (Momentum) Program)
  2. National Research, Development and Innovation Office (NKFIH) (ERC_HU) [PD 131543, KKP_19, TKP2021-EGA-04]
  3. Ministry for National Economy [VEKOP 2.2.1-16]

向作者/读者索取更多资源

There is a growing demand for bacteria repellent surfaces and antibody-based coatings in the field of biosensors. The optical waveguide lightmode spectroscopy (OWLS) technique offers a non-invasive and label-free method for characterizing protein and bacterial adsorption. In this study, an OWLS-based method was used to develop bacteria repellent surfaces and characterize different antibody-based coatings for bacterial assays. Nonspecific binding blocking agents were tested and immobilization methods for selected antibodies were applied. The performance of the biosensor was evaluated using enzyme-linked immunosorbent assay (ELISA) measurements. The best performance was achieved with a polyclonal antibody in combination with protein A-based immobilization and blocking of nonspecific binding.
Bacteria repellent surfaces and antibody-based coatings for bacterial assays have shown a growing demand in the field of biosensors, and have crucial importance in the design of biomedical devices. However, in-depth investigations and comparisons of possible solutions are still missing. The optical waveguide lightmode spectroscopy (OWLS) technique offers label-free, non-invasive, in situ characterization of protein and bacterial adsorption. Moreover, it has excellent flexibility for testing various surface coatings. Here, we describe an OWLS-based method supporting the development of bacteria repellent surfaces and characterize the layer structures and affinities of different antibody-based coatings for bacterial assays. In order to test nonspecific binding blocking agents against bacteria, OWLS chips were coated with bovine serum albumin (BSA), I-block, PAcrAM-g-(PMOXA, NH2, Si), (PAcrAM-P) and PLL-g-PEG (PP) (with different coating temperatures), and subsequent Escherichia coli adhesion was monitored. We found that the best performing blocking agents could inhibit bacterial adhesion from samples with bacteria concentrations of up to 10(7) cells/mL. Various immobilization methods were applied to graft a wide range of selected antibodies onto the biosensor's surface. Simple physisorption, Mix&Go (AnteoBind) (MG) films, covalently immobilized protein A and avidin-biotin based surface chemistries were all fabricated and tested. The surface adsorbed mass densities of deposited antibodies were determined, and the biosensor;s kinetic data were evaluated to divine the possible orientations of the bacteria-capturing antibodies and determine the rate constants and footprints of the binding events. The development of affinity layers was supported by enzyme-linked immunosorbent assay (ELISA) measurements in order to test the bacteria binding capabilities of the antibodies. The best performance in the biosensor measurements was achieved by employing a polyclonal antibody in combination with protein A-based immobilization and PAcrAM-P blocking of nonspecific binding. Using this setting, a surface sensitivity of 70 cells/mm(2) was demonstrated.

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