Literature DB >> 22688388

A liquid phase affinity capture assay using magnetic beads to study protein-protein interaction: the poliovirus-nanobody example.

Lise Schotte1, Bart Rombaut, Bert Thys.   

Abstract

In this article, a simple, quantitative, liquid phase affinity capture assay is presented. Provided that one protein can be tagged and another protein labeled, this method can be implemented for the investigation of protein-protein interactions. It is based on one hand on the recognition of the tagged protein by cobalt coated magnetic beads and on the other hand on the interaction between the tagged protein and a second specific protein that is labeled. First, the labeled and tagged proteins are mixed and incubated at room temperature. The magnetic beads, that recognize the tag, are added and the bound fraction of labeled protein is separated from the unbound fraction using magnets. The amount of labeled protein that is captured can be determined in an indirect way by measuring the signal of the labeled protein remained in the unbound fraction. The described liquid phase affinity assay is extremely useful when conformational conversion sensitive proteins are assayed. The development and application of the assay is demonstrated for the interaction between poliovirus and poliovirus recognizing nanobodies(1). Since poliovirus is sensitive to conformational conversion(2) when attached to a solid surface (unpublished results), the use of ELISA is limited and a liquid phase based system should therefore be preferred. An example of a liquid phase based system often used in polioresearch(3,4) is the micro protein A-immunoprecipitation test(5). Even though this test has proven its applicability, it requires an Fc-structure, which is absent in the nanobodies(6,7). However, as another opportunity, these interesting and stable single-domain antibodies(8) can be easily engineered with different tags. The widely used (His)(6)-tag shows affinity for bivalent ions such as nickel or cobalt, which can on their turn be easily coated on magnetic beads. We therefore developed this simple quantitative affinity capture assay based on cobalt coated magnetic beads. Poliovirus was labeled with (35)S to enable unhindered interaction with the nanobodies and to make a quantitative detection feasible. The method is easy to perform and can be established with a low cost, which is further supported by the possibility of effectively regenerating the magnetic beads.

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Year:  2012        PMID: 22688388      PMCID: PMC3468194          DOI: 10.3791/3937

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  13 in total

1.  Rapid isolation of antigens from cells with a staphylococcal protein A-antibody adsorbent: parameters of the interaction of antibody-antigen complexes with protein A.

Authors:  S W Kessler
Journal:  J Immunol       Date:  1975-12       Impact factor: 5.422

2.  Fluorescence labeling of human rhinovirus capsid and analysis by capillary electrophoresis.

Authors:  Leopold Kremser; Tünde Konecsni; Dieter Blaas; Ernst Kenndler
Journal:  Anal Chem       Date:  2004-07-15       Impact factor: 6.986

3.  A simple quantitative affinity capturing assay of poliovirus antigens and subviral particles by single-domain antibodies using magnetic beads.

Authors:  Bert Thys; Dirk Saerens; Lise Schotte; Gerrit De Bleeser; Serge Muyldermans; Gholamreza Hassanzadeh-Ghassabeh; Bart Rombaut
Journal:  J Virol Methods       Date:  2011-03-01       Impact factor: 2.014

4.  A competition immunoprecipitation assay of unlabeled poliovirus antigens.

Authors:  B Rombaut; J Jore; A Boeyé
Journal:  J Virol Methods       Date:  1994-06       Impact factor: 2.014

5.  Epitope evolution in poliovirus maturation.

Authors:  B Rombaut; R Vrijsen; A Boeyé
Journal:  Arch Virol       Date:  1983       Impact factor: 2.574

6.  Hybridoma antibodies to poliovirus N and H antigen.

Authors:  P Brioen; R J Sijens; R Vrijsen; B Rombaut; A A Thomas; A Jackers; A Boeyé
Journal:  Arch Virol       Date:  1982       Impact factor: 2.574

Review 7.  Single domain camel antibodies: current status.

Authors:  S Muyldermans
Journal:  J Biotechnol       Date:  2001-06       Impact factor: 3.307

8.  Caveolar endocytosis of simian virus 40 reveals a new two-step vesicular-transport pathway to the ER.

Authors:  L Pelkmans; J Kartenbeck; A Helenius
Journal:  Nat Cell Biol       Date:  2001-05       Impact factor: 28.824

9.  A study of the cross-reacting antigens on the intact foot-and-mouth disease virus and its 12S Subunits with antisera against the structural proteins.

Authors:  R H Meloen; J Briaire
Journal:  J Gen Virol       Date:  1980-11       Impact factor: 3.891

10.  Naturally occurring antibodies devoid of light chains.

Authors:  C Hamers-Casterman; T Atarhouch; S Muyldermans; G Robinson; C Hamers; E B Songa; N Bendahman; R Hamers
Journal:  Nature       Date:  1993-06-03       Impact factor: 49.962

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