Expressed murine and human CDR-H3 intervals of equal length exhibit distinct repertoires that differ in their amino acid composition and predicted range of structures.
about
Toward high-resolution homology modeling of antibody Fv regions and application to antibody-antigen dockingEngineered IgG1-Fc--one fragment to bind them allDeep sequencing in library selection projects: what insight does it bring?In situ click chemistry: from small molecule discovery to synthetic antibodiesHigh-affinity single-domain binding proteins with a binary-code interfaceA Dominant Conformational Role for Amino Acid Diversity in Minimalist Protein–Protein InterfacesAn Ultra-specific Avian Antibody to Phosphorylated Tau Protein Reveals a Unique Mechanism for Phosphoepitope RecognitionCDR-H3 Diversity Is Not Required for Antigen Recognition by Synthetic AntibodiesA Reverse Binding Motif That Contributes to Specific Protease Inhibition by AntibodiesSupersite of immune vulnerability on the glycosylated face of HIV-1 envelope glycoprotein gp120Rabbit Anti-HIV-1 Monoclonal Antibodies Raised by Immunization Can Mimic the Antigen-Binding Modes of Antibodies Derived from HIV-1-Infected HumansStructure and specificity of an antibody targeting a proteolytically cleaved IgG hingeEngineering of recombinant crystallization chaperonesSnugDock: paratope structural optimization during antibody-antigen docking compensates for errors in antibody homology modelsSingle cycle structure-based humanization of an anti-nerve growth factor therapeutic antibodyImmunoglobulin heavy chain diversity in Pteropid bats: evidence for a diverse and highly specific antigen binding repertoireHumanized Immunoglobulin Mice: Models for HIV Vaccine Testing and Studying the Broadly Neutralizing Antibody Problem.Systematic analysis of short internal indels and their impact on protein folding.Synthetic antibodies from a four-amino-acid code: a dominant role for tyrosine in antigen recognition.Antibody binding loop insertions as diversity elementsA focused antibody library for selecting scFvs expressed at high levels in the cytoplasm.Amino acid alphabet size in protein evolution experiments: better to search a small library thoroughly or a large library sparsely?Investigating the properties of Bacillus thuringiensis Cry proteins with novel loop replacements created using combinatorial molecular biology.The importance of being tyrosine: lessons in molecular recognition from minimalist synthetic binding proteins.Precise determination of the diversity of a combinatorial antibody library gives insight into the human immunoglobulin repertoire.The functional repertoire of rabbit antibodies and antibody discovery via next-generation sequencing.Stability and CDR composition biases enrich binder functionality landscapes.Rare antibodies from combinatorial libraries suggests an S.O.S. component of the human immunological repertoire.Comparative analysis of human and mouse immunoglobulin variable heavy regions from IMGT/LIGM-DB with IMGT/HighV-QUEST.Comparison of antibody repertoires produced by HIV-1 infection, other chronic and acute infections, and systemic autoimmune disease.Identification of nitrated immunoglobulin variable regions in the HIV-infected human brain: implications in HIV infection and immune response.ScaffoldSeq: Software for characterization of directed evolution populations.Selection of a CXCR4 antagonist from a human heavy chain CDR3-derived phage library.The promise and challenge of high-throughput sequencing of the antibody repertoire.Antibody V(h) repertoire differences between resolving and chronically evolving hepatitis C virus infections.Structure of the Fab fragment of F105, a broadly reactive anti-human immunodeficiency virus (HIV) antibody that recognizes the CD4 binding site of HIV type 1 gp120.Expressed antibody repertoires in human cord blood cells: 454 sequencing and IMGT/HighV-QUEST analysis of germline gene usage, junctional diversity, and somatic mutations.Characterization of a high-affinity human antibody with a disulfide bridge in the third complementarity-determining region of the heavy chain.Structural basis for the recognition of human cytomegalovirus glycoprotein B by a neutralizing human antibodyTransferring the characteristics of naturally occurring and biased antibody repertoires to human antibody libraries by trapping CDRH3 sequences
P2860
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P2860
Expressed murine and human CDR-H3 intervals of equal length exhibit distinct repertoires that differ in their amino acid composition and predicted range of structures.
description
2003 nî lūn-bûn
@nan
2003 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Expressed murine and human CDR ...... predicted range of structures.
@ast
Expressed murine and human CDR ...... predicted range of structures.
@en
type
label
Expressed murine and human CDR ...... predicted range of structures.
@ast
Expressed murine and human CDR ...... predicted range of structures.
@en
prefLabel
Expressed murine and human CDR ...... predicted range of structures.
@ast
Expressed murine and human CDR ...... predicted range of structures.
@en
P2093
P1476
Expressed murine and human CDR ...... predicted range of structures.
@en
P2093
Cosima Zemlin
Harry W Schroeder
Jeffrey A Engler
Karl Bauer
Martin Klinger
Perry M Kirkham
P304
P356
10.1016/J.JMB.2003.10.007
P407
P577
2003-12-01T00:00:00Z