Ribosome display efficiently selects and evolves high-affinity antibodies in vitro from immune libraries. - Wikidata - awgldk - TriplyDB

Ribosome display efficiently selects and evolves high-affinity antibodies in vitro from immune libraries.

Ribosome display efficiently selects and evolves high-affinity antibodies in vitro from immune libraries.

http://www.wikidata.org/entity/Q31967754

about

Molecular immunolabeling with recombinant single-chain variable fragment (scFv) antibodies designed with metal-binding domains mRNA display: diversity matters during in vitro selection The use of mRNA display to select high-affinity protein-binding peptides Remodeling a DNA-binding protein as a specific in vivo inhibitor of bacterial secretin PulD Oligonucleotide-assisted cleavage and ligation: a novel directional DNA cloning technology to capture cDNAs. Application in the construction of a human immune antibody phage-display library Directed in vitro evolution and crystallographic analysis of a peptide-binding single chain antibody fragment (scFv) with low picomolar affinity Structure-based Protocol for Identifying Mutations that Enhance Protein–Protein Binding Affinities Development of a generic adenovirus delivery system based on structure-guided design of bispecific trimeric DARPin adapters Yeast mating for combinatorial Fab library generation and surface display The role of dynamic conformational ensembles in biomolecular recognition Comparison of Escherichia coli and rabbit reticulocyte ribosome display systems.Investigating and Engineering Enzymes by Genetic Selection.Antigen-independent selection of stable intracellular single-chain antibodies.Direct in vivo screening of intrabody libraries constructed on a highly stable single-chain framework.Efficient isolation of soluble intracellular single-chain antibodies using the twin-arginine translocation machinery.The periplasmic Escherichia coli peptidylprolyl cis,trans-isomerase FkpA. I. Increased functional expression of antibody fragments with and without cis-prolines.Functional selection of vaccine candidate peptides from Staphylococcus aureus whole-genome expression libraries in vitro.Tailoring in vitro evolution for protein affinity or stability.Fine tuning of the specificity of an anti-progesterone antibody by first and second sphere residue engineering.An antibody library for stabilizing and crystallizing membrane proteins - selecting binders to the citrate carrier CitS.Ribosome display for improved biotherapeutic molecules.Isolation of anti-CD22 Fv with high affinity by Fv display on human cells.Optimizing the affinity and specificity of proteins with molecular display.Affinity-matured recombinant antibody fragments analyzed by single-molecule force spectroscopy Use of cDNA tiling arrays for identifying protein interactions selected by in vitro display technologies.Synthetic antibody libraries focused towards peptide ligands.Selection of anti-sulfadimidine specific ScFvs from a hybridoma cell by eukaryotic ribosome display.Spatially addressed combinatorial protein libraries for recombinant antibody discovery and optimization.Her2-specific multivalent adapters confer designed tropism to adenovirus for gene targeting Immunogenomic engineering of a plug-and-(dis)play hybridoma platform.Generation and Characterization of an scFv Directed against Site II of Rabies Glycoprotein.A label-free immunosensor array using single-chain antibody fragments.Arrayed protein library technology for therapeutic biologic discovery.Detection of biomarkers using recombinant antibodies coupled to nanostructured platforms Antibody isolation from immunized animals: comparison of phage display and antibody discovery via V gene repertoire mining.Affinity maturation of antiHER2 monoclonal antibody MIL5 using an epitope-specific synthetic phage library by computational design.Selection of single chain variable fragments specific for the human-inducible costimulator using ribosome display.The influence of antibody fragment format on phage display based affinity maturation of IgG.Novel Human Three-Domain Antibody Fragments Against sTNFα as Well as tmTNFα with High Affinity Generated by the Combination of Ribosome Display and E. coli Expression System.Three Recombinant Engineered Antibodies against Recombinant Tags with High Affinity and Specificity

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P2860

Ribosome display efficiently selects and evolves high-affinity antibodies in vitro from immune libraries.

http://www.wikidata.org/entity/Q31967754

description

1998 nî lūn-bûn

@nan

1998 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

1998 թվականի նոյեմբերին հրատարակված գիտական հոդված

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1998年の論文

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1998年論文

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1998年論文

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1998年論文

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1998年論文

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1998年論文

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1998年论文

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name

Ribosome display efficiently s ...... n vitro from immune libraries.

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Ribosome display efficiently s ...... n vitro from immune libraries.

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type

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Ribosome display efficiently s ...... n vitro from immune libraries.

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Ribosome display efficiently s ...... n vitro from immune libraries.

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prefLabel

Ribosome display efficiently s ...... n vitro from immune libraries.

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Ribosome display efficiently s ...... n vitro from immune libraries.

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PNAS.95.24.14130

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Ribosome display efficiently s ...... in vitro from immune libraries

@en

P2093

H R Bosshard

http://www.w3.org/2001/XMLSchema#string

J Hanes

http://www.w3.org/2001/XMLSchema#string

L Jermutus

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S Weber-Bornhauser

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P2860

An in vitro polysome display system for identifying ligands from very large peptide libraries

In vitro selection and evolution of functional proteins by using ribosome display

RNA-peptide fusions for the in vitro selection of peptides and proteins

The leucine zipper: a hypothetical structure common to a new class of DNA binding proteins

Calculation of protein extinction coefficients from amino acid sequence data

GCN4 protein, synthesized in vitro, binds HIS3 regulatory sequences: implications for general control of amino acid biosynthetic genes in yeast.

Rapid evolution of a protein in vitro by DNA shuffling

Human antibodies with sub-nanomolar affinities isolated from a large non-immunized phage display library.

Molecular evolution by staggered extension process (StEP) in vitro recombination.

Antibody-ribosome-mRNA (ARM) complexes as efficient selection particles for in vitro display and evolution of antibody combining sites.

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14130-14135

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24

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95

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Andreas Plückthun

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1998-11-01T00:00:00Z

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13459398

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9826665

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24338

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