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Book ChapterDOI

Selection of Recombinant Human Antibodies.

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TLDR
In this review, different technologies that are currently used for the in vitro and in vivo generation of human antibodies are described.
Abstract
Since the development of therapeutic antibodies the demand of recombinant human antibodies is steadily increasing. Traditionally, therapeutic antibodies were generated by immunization of rat or mice, the generation of hybridoma clones, cloning of the antibody genes and subsequent humanization and engineering of the lead candidates. In the last few years, techniques were developed that use transgenic animals with a human antibody gene repertoire. Here, modern recombinant DNA technologies can be combined with well established immunization and hybridoma technologies to generate already affinity maturated human antibodies. An alternative are in vitro technologies which enabled the generation of fully human antibodies from antibody gene libraries that even exceed the human antibody repertoire. Specific antibodies can be isolated from these libraries in a very short time and therefore reduce the development time of an antibody drug at a very early stage.In this review, we describe different technologies that are currently used for the in vitro and in vivo generation of human antibodies.

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Journal ArticleDOI

Opportunities for therapeutic antibodies directed at G-protein-coupled receptors

TL;DR: The progress made by targeting GPCRs with antibody-based therapeutics, as well as technical hurdles to overcome, are presented and discussed in this Review.
Journal ArticleDOI

Peptides, Antibodies, Peptide Antibodies and More.

TL;DR: The applications of peptides and antibodies to multiple targets have emerged as powerful tools in research, diagnostics, vaccine development, and therapeutics and remain crucial reagents in molecular biology.

Multi-subunit proteins onthesurface offilamentous phage: methodologies fordisplaying antibody (Fab) heavyand light chains

Peter Hudson
TL;DR: In this paper, the authors show that FabFragments can be assembled onthesurface of the phage by linking one chain to thephage coat protein, and hiding the other in the bacterial periplasm.
Book ChapterDOI

Construction of Synthetic Antibody Phage-Display Libraries

TL;DR: This protocol describes the construction of synthetic antibody libraries based on a single engineered human autonomous variable heavy domain scaffold with diversity in all three complementarity-determining regions.
Journal ArticleDOI

Recombinant antibodies and their use for food immunoanalysis

TL;DR: In this paper, the characteristics, advantages, and disadvantages of recombinant antibodies including antigen-binding fragments (Fab), single-chain fragment variable (scFv), and single-domain antibodies (VHH) and their application in food analysis with especial emphasis on the analysis of biotoxins, antibiotics, pesticides, and foodborne pathogens.
References
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Journal ArticleDOI

Continuous cultures of fused cells secreting antibody of predefined specificity

TL;DR: The derivation of a number of tissue culture cell lines which secrete anti-sheep red blood cell (SRBC) antibodies is described here, made by fusion of a mouse myeloma and mouse spleen cells from an immunised donor.
Journal ArticleDOI

Filamentous fusion phage: novel expression vectors that display cloned antigens on the virion surface

TL;DR: Foreign DNA fragments can be inserted into filamentous phage gene III to create a fusion protein with the foreign sequence in the middle that is incorporated into the virion, which retains infectivity and displays the foreign amino acids in immunologically accessible form.
Journal ArticleDOI

Phage antibodies: filamentous phage displaying antibody variable domains

TL;DR: It is shown that complete antibody V domains can be displayed on the surface of fd bacteriophage, that the phage bind specifically to antigen and that rare phage can be isolated after affinity chromatography.
Journal ArticleDOI

Interleukin-13: Central Mediator of Allergic Asthma

TL;DR: In this paper, the type 2 cytokine IL-13, which shares a receptor component and signaling pathways with IL-4, was found to be necessary and sufficient for the expression of allergic asthma.
Journal ArticleDOI

Rapid evolution of a protein in vitro by DNA shuffling.

Willem P. C. Stemmer
- 04 Aug 1994 - 
TL;DR: It is reported here that selected mutants had a minimum inhibitory concentration of 640 μg ml-1, a 32,000-fold increase and 64-fold greater than any published TEM-1 derived enzyme.
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