2-D protein crystals as an immobilization matrix for producing reaction zones in dipstick-style immunoassays
In the present study, the applicability of crystalline bacterial cell-surface layers (S-layers) as novel immobilization matrices and reaction zones for dipstick-style immunoassays was investigated. For this purpose, S-layer-carrying cell-wall fragments from Bacillus sphaericus CCM 2120 were deposite...
Veröffentlicht in: | BioTechniques. - 1993. - 21(1996), 5 vom: 21. Nov., Seite 918-25 |
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1. Verfasser: | |
Weitere Verfasser: | , , , , , , , |
Format: | Aufsatz |
Sprache: | English |
Veröffentlicht: |
1996
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Zugriff auf das übergeordnete Werk: | BioTechniques |
Schlagworte: | Journal Article Research Support, Non-U.S. Gov't Antibodies, Monoclonal Bacterial Proteins Immunoglobulin G Staphylococcal Protein A Streptavidin 9013-20-1 |
Zusammenfassung: | In the present study, the applicability of crystalline bacterial cell-surface layers (S-layers) as novel immobilization matrices and reaction zones for dipstick-style immunoassays was investigated. For this purpose, S-layer-carrying cell-wall fragments from Bacillus sphaericus CCM 2120 were deposited on a microporous support, and the S-layer protein was cross-linked with glutaraldehyde. For developing appropriate test systems, either human IgG was directly linked to the carboxylic acid groups from the S-layer protein or it was immobilized using Protein A or, after biotinylation, using streptavidin. A clear correlation was obtained between the amount of anti-human IgG applied and the absorbance values in the immunoassays. S-layers with covalently bound recombinant major birch pollen allergen were used for quantitative and semiquantitative determination of an antibody raised against it. Using S-layers as an immobilization matrix in comparison to amorphous polymers has advantages in that the closed monolayers of functional macromolecules on their outermost surface allows for strong signals in immunoassays, almost completely eliminates background and prevents diffusion |
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Beschreibung: | Date Completed 20.02.1997 Date Revised 28.09.2018 published: Print Citation Status MEDLINE |
ISSN: | 0736-6205 |