Extending half-life by indirect targeting of the neonatal Fc receptor (FcRn) using a minimal albumin binding domain.
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Fusion Proteins for Half-Life Extension of Biologics as a Strategy to Make BiobettersUnraveling the Interaction between FcRn and Albumin: Opportunities for Design of Albumin-Based TherapeuticsFusion to a highly stable consensus albumin binding domain allows for tunable pharmacokineticsThe neonatal Fc receptor, FcRn, as a target for drug delivery and therapyEngineering of bispecific affinity proteins with high affinity for ERBB2 and adaptable binding to albuminEngineering bispecificity into a single albumin-binding domain.Bacterial display in combinatorial protein engineering.In vivo targeting of HER2-positive tumor using 2-helix affibody molecules.Selection of nanobodies that target human neonatal Fc receptor.Repeated acetylcholine receptor antibody-concentrations and association to clinical myasthenia gravis development.Development and characterization of small bispecific albumin-binding domains with high affinity for ErbB3.Engineered antibody variable and constant domains as therapeutic candidates.Novel exenatide analogs with peptidic albumin binding domains: potent anti-diabetic agents with extended duration of actionThe albumin-binding domain as a scaffold for protein engineering.Genetically engineered humanized mouse models for preclinical antibody studies.A truncated and dimeric format of an Affibody library on bacteria enables FACS-mediated isolation of amyloid-beta aggregation inhibitors with subnanomolar affinity.Albumin-binding domain conjugate for near-infrared fluorescence lymphatic imaging.Monoclonal antibodies directed against human FcRn and their applications.Protease substrate profiling using bacterial display of self-blocking affinity proteins and flow-cytometric sorting.Absorption, distribution, metabolism, and excretion (ADME) studies of biotherapeutics for autoimmune and inflammatory conditions.Engineering neonatal Fc receptor-mediated recycling and transcytosis in recombinant proteins by short terminal peptide extensions.A series of anti-CEA/anti-DOTA bispecific antibody formats evaluated for pre-targeting: comparison of tumor uptake and blood clearance.Long-acting recombinant coagulation factor IX albumin fusion protein (rIX-FP) in hemophilia B: results of a phase 3 trial.Improved in vivo anti-tumor effects of IgA-Her2 antibodies through half-life extension and serum exposure enhancement by FcRn targetingFab-dsFv: A bispecific antibody format with extended serum half-life through albumin binding.Evaluation of an Albumin-Binding Domain Protein Fused to Recombinant Human IL-2 and Its Effects on the Bioactivity and Serum Half-Life of the Cytokine.In vivo evaluation of a novel format of a bivalent HER3-targeting and albumin-binding therapeutic affibody construct.Candidate antibody-based therapeutics against HIV-1.Design and evaluation of radiolabeled tracers for tumor imaging.Fatty Acid-Modified Gapmer Antisense Oligonucleotide and Serum Albumin Constructs for Pharmacokinetic Modulation.Novel affinity binders for neutralization of vascular endothelial growth factor (VEGF) signaling.Engineering of a bispecific affibody molecule towards HER2 and HER3 by addition of an albumin-binding domain allows for affinity purification and in vivo half-life extension.Recent advances in (therapeutic protein) drug development.Extending the half-life of a fab fragment through generation of a humanized anti-human serum albumin Fv domain: An investigation into the correlation between affinity and serum half-life.Dissection of the neonatal Fc receptor (FcRn)-albumin interface using mutagenesis and anti-FcRn albumin-blocking antibodiesPharmacokinetics and mechanisms of plasma removal of hemoglobin-based oxygen carriers.TAT-HSA-α-MSH fusion protein with extended half-life inhibits tumor necrosis factor-α in brain inflammation of mice.Oral delivery of anti-MDM2 inhibitor SP141-loaded FcRn-targeted nanoparticles to treat breast cancer and metastasis.Therapeutic impact of human serum albumin-thioredoxin fusion protein on influenza virus-induced lung injury mice.Interaction with both domain I and III of albumin is required for optimal pH-dependent binding to the neonatal Fc receptor (FcRn).
P2860
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P2860
Extending half-life by indirect targeting of the neonatal Fc receptor (FcRn) using a minimal albumin binding domain.
description
2010 nî lūn-bûn
@nan
2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Extending half-life by indirec ...... inimal albumin binding domain.
@ast
Extending half-life by indirec ...... inimal albumin binding domain.
@en
Extending half-life by indirect targeting of the neonatal Fc receptor
@nl
type
label
Extending half-life by indirec ...... inimal albumin binding domain.
@ast
Extending half-life by indirec ...... inimal albumin binding domain.
@en
Extending half-life by indirect targeting of the neonatal Fc receptor
@nl
prefLabel
Extending half-life by indirec ...... inimal albumin binding domain.
@ast
Extending half-life by indirec ...... inimal albumin binding domain.
@en
Extending half-life by indirect targeting of the neonatal Fc receptor
@nl
P2093
P2860
P356
P1476
Extending half-life by indirec ...... inimal albumin binding domain.
@en
P2093
Caroline Ekblad
Jan Terje Andersen
Lars Abrahmsén
Muluneh Bekele Daba
Rikard Pehrson
Vladimir Tolmachev
P2860
P304
P356
10.1074/JBC.M110.164848
P407
P577
2010-12-07T00:00:00Z