Constructing high complexity synthetic libraries of long ORFs using in vitro selection.
about
The use of mRNA display to select high-affinity protein-binding peptidesMulti-line split DNA synthesis: a novel combinatorial method to make high quality peptide librariesDomain structure and protein interactions of the silent information regulator Sir3 revealed by screening a nested deletion library of protein fragments.Functional proteins from a random-sequence libraryComparison of the frequency of functional SH3 domains with different limited sets of amino acids using mRNA display.Investigating and Engineering Enzymes by Genetic Selection.Large libraries reveal diverse solutions to an RNA recognition problem.Random multi-recombinant PCR for the construction of combinatorial protein librariesSelection of proteins with desired properties from natural proteome libraries using mRNA display.Sequence analysis of an artificial family of RNA-binding peptidesAn intein-based genetic selection allows the construction of a high-quality library of binary patterned de novo protein sequences.Construction and characterization of protein libraries composed of secondary structure modules.Combinatorial approaches to novel proteins.Selection and evolution of enzymes from a partially randomized non-catalytic scaffold.Comparative characterization of random-sequence proteins consisting of 5, 12, and 20 kinds of amino acids.Scanning the human proteome for calmodulin-binding proteins.mRNA display for the selection and evolution of enzymes from in vitro-translated protein libraries.Experimental mapping of soluble protein domains using a hierarchical approachmRNA display using covalent coupling of mRNA to translated proteins.mRNA display-based selections using synthetic peptide and natural protein libraries.Engineering of biocatalysts - from evolution to creation.In vitro selection of proteins with desired characteristics using mRNA-display.Design, expression, and purification of de novo transmembrane "hairpin" peptides.Development of Next-Generation Peptide Binders Using In vitro Display Technologies and Their Potential Applications.Inhibition of proteolysis and other posttranslational modifications with substrate-targeted inhibitors.Highly diverse protein library based on the ubiquitous (β/α)₈ enzyme fold yields well-structured proteins through in vitro folding selection.In vitro affinity screening of protein and peptide binders by megavalent bead surface display.An overhang-based DNA block shuffling method for creating a customized random library.Reverse Engineering of Vaccine Antigens Using High Throughput Sequencing-enhanced mRNA DisplayReprogramming eukaryotic translation with ligand-responsive synthetic RNA switches.Characterization of endogenous and recombinant human calpain-10Oligonucleotide-directed site-specific integration of high complexity libraries into ssDNA templatesHighly stable and efficient mRNA templates for mRNA-protein fusions and C-terminally labeled proteinsDirected Evolution of Glycopeptides Using mRNA Display.
P2860
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P2860
Constructing high complexity synthetic libraries of long ORFs using in vitro selection.
description
2000 nî lūn-bûn
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2000年の論文
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2000年論文
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name
Constructing high complexity synthetic libraries of long ORFs using in vitro selection.
@ast
Constructing high complexity synthetic libraries of long ORFs using in vitro selection.
@en
type
label
Constructing high complexity synthetic libraries of long ORFs using in vitro selection.
@ast
Constructing high complexity synthetic libraries of long ORFs using in vitro selection.
@en
prefLabel
Constructing high complexity synthetic libraries of long ORFs using in vitro selection.
@ast
Constructing high complexity synthetic libraries of long ORFs using in vitro selection.
@en
P2093
P356
P1476
Constructing high complexity synthetic libraries of long ORFs using in vitro selection.
@en
P2093
P304
P356
10.1006/JMBI.2000.3571
P407
P577
2000-03-01T00:00:00Z