Literature DB >> 10594359

Fluobodies: green fluorescent single-chain Fv fusion proteins.

R A Griep1, C van Twisk, J M van der Wolf, A Schots.   

Abstract

An expression system (pSKGFP), which permits the expression of single-chain variable fragments as fusion proteins with modified green fluorescent proteins, was designed. This expression system is comparable to frequently used phage display vectors and allows single-step characterization of the selected recombinant antibodies by flow cytometry or fluorescent cell staining. Two different single-chain variable fragment antibodies, both directed against the lipopolysaccharide of the bacterium Ralstonia solanacearum have been genetically fused to a red-shifted green fluorescent protein and the produced fusion protein tested for usefulness. These fluobodies can be produced in cultures of bacterial cells and purified using immobilized metal affinity chromatography. They function well in flow cytometry and immunofluorescent cell staining, are specific for their target antigens and, unlike FITC-conjugated antibodies, they do not fade upon illumination.

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Year:  1999        PMID: 10594359     DOI: 10.1016/s0022-1759(99)00131-3

Source DB:  PubMed          Journal:  J Immunol Methods        ISSN: 0022-1759            Impact factor:   2.303


  13 in total

Review 1.  The production and application of single-chain antibody fragments.

Authors:  D Blazek; V Celer
Journal:  Folia Microbiol (Praha)       Date:  2003       Impact factor: 2.099

2.  Fluorescent IgG fusion proteins made in E. coli.

Authors:  Yael Luria; Dina Raichlin; Itai Benhar
Journal:  MAbs       Date:  2012-04-26       Impact factor: 5.857

3.  Fluorescent Citrine-IgG fusion proteins produced in mammalian cells.

Authors:  Alexander K Haas; Christoffer von Schwerin; Daniela Matscheko; Ulrich Brinkmann
Journal:  MAbs       Date:  2010-11-01       Impact factor: 5.857

4.  Module based antibody engineering: a novel synthetic REDantibody.

Authors:  Anatoliy Markiv; Bernard Anani; Ravi V Durvasula; Angray S Kang
Journal:  J Immunol Methods       Date:  2010-11-03       Impact factor: 2.303

5.  Phage-displayed combinatorial peptide libraries in fusion to beta-lactamase as reporter for an accelerated clone screening: Potential uses of selected enzyme-linked affinity reagents in downstream applications.

Authors:  Girja S Shukla; David N Krag
Journal:  Comb Chem High Throughput Screen       Date:  2010-01       Impact factor: 1.339

6.  Generation of Fab fragment-like molecular recognition proteins against staphylococcal enterotoxin B by phage display technology.

Authors:  Yuji Urushibata; Kunihiko Itoh; Motohiro Ohshima; Yasuo Seto
Journal:  Clin Vaccine Immunol       Date:  2010-09-15

7.  A yeast platform for the production of single-chain antibody-green fluorescent protein fusions.

Authors:  Dagang Huang; Eric V Shusta
Journal:  Appl Environ Microbiol       Date:  2006-10-06       Impact factor: 4.792

8.  Fluorescent labeling of antibody fragments using split GFP.

Authors:  Fortunato Ferrara; Pawel Listwan; Geoffrey S Waldo; Andrew R M Bradbury
Journal:  PLoS One       Date:  2011-10-05       Impact factor: 3.240

9.  Expression of recombinant multi-coloured fluorescent antibodies in gor -/trxB- E. coli cytoplasm.

Authors:  Anatoliy Markiv; Richard Beatson; Joy Burchell; Ravi V Durvasula; Angray S Kang
Journal:  BMC Biotechnol       Date:  2011-11-30       Impact factor: 2.563

Review 10.  scFv antibody: principles and clinical application.

Authors:  Zuhaida Asra Ahmad; Swee Keong Yeap; Abdul Manaf Ali; Wan Yong Ho; Noorjahan Banu Mohamed Alitheen; Muhajir Hamid
Journal:  Clin Dev Immunol       Date:  2012-03-15
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