Literature DB >> 31548440

Stepwise Preparation of a Polymer Comprising Protein Building Blocks on a Solid Support for Immunosensing Platform.

Hiroki Miyao1, Utaro Uemura1, Shinji Sueda2,3.   

Abstract

In immunosensing, immobilization of the antibody on the sensing platform significantly influences the performance of the sensor. Herein, we propose a novel antibody-immobilization method based on a protein-polymer chain containing multiple copies of an antibody-binding protein, the Z-domain. In our approach, the Z-domain-containing polymer is prepared on the surface of the sensing platform with a biotinylation reaction from the archaeon Sulfolobus tokodaii. Biotinylation from S. tokodaii has a unique property by which biotin protein ligase (BPL) forms an extremely stable complex with its biotinylated substrate protein (BCCP). Here, we employed two types of engineered proteins: one was the fusion protein of BCCP with the Z-domain (BZB), in which BCCP was genetically attached to the N- and C-termini of the Z-domain; the other was a BPL dimer prepared by connecting two BPL molecules with a cross-linking reagent. We applied these two engineered proteins alternately onto the BPL-modified solid support of the surface plasmon resonance sensor chip, and succeeded in growing polymer chains comprising multiple units of BZB and the BPL dimer. The antibody-binding capability of the Z-domain-containing polymer thus prepared is adjustable by controlling the number of cycles of protein addition and the surface density of the polymer on the solid support.

Entities:  

Keywords:  Immunosensor; Z-domain; antibody-binding protein; biotinylation; protein interaction; surface plasmon resonance

Mesh:

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Year:  2019        PMID: 31548440     DOI: 10.2116/analsci.19P318

Source DB:  PubMed          Journal:  Anal Sci        ISSN: 0910-6340            Impact factor:   1.967


  1 in total

Review 1.  Tag-mediated single-step purification and immobilization of recombinant proteins toward protein-engineered advanced materials.

Authors:  Ana I Freitas; Lucília Domingues; Tatiana Q Aguiar
Journal:  J Adv Res       Date:  2021-06-15       Impact factor: 10.479

  1 in total

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