Chemoenzymatic Fc glycosylation via engineered aldehyde tags.
about
Intramolecular N-glycan/polypeptide interactions observed at multiple N-glycan remodeling steps through [(13)C,(15)N]-N-acetylglucosamine labeling of immunoglobulin G1.Site-specific antibody-drug conjugates: the nexus of bioorthogonal chemistry, protein engineering, and drug developmentBacterial glycosidases in pathogenesis and glycoengineering.Methods to Make Homogenous Antibody Drug Conjugates.Glycoengineered Monoclonal Antibodies with Homogeneous Glycan (M3, G0, G2, and A2) Using a Chemoenzymatic Approach Have Different Affinities for FcγRIIIa and Variable Antibody-Dependent Cellular Cytotoxicity Activities.Native mass spectrometry and ion mobility characterization of trastuzumab emtansine, a lysine-linked antibody drug conjugate.Site-Specific Glycoconjugation of Protein via Bioorthogonal Tetrazine Cycloaddition with a Genetically Encoded trans-Cyclooctene or Bicyclononyne.High Yield Expression of Recombinant Human Proteins with the Transient Transfection of HEK293 Cells in Suspension.Formylglycine, a post-translationally generated residue with unique catalytic capabilities and biotechnology applications.Protein-polymer therapeutics: a macromolecular perspective.Cutting-edge mass spectrometry methods for the multi-level structural characterization of antibody-drug conjugates.Peptide-tags for site-specific protein labelling in vitro and in vivo.Structurally Defined αMHC-II Nanobody-Drug Conjugates: A Therapeutic and Imaging System for B-Cell Lymphoma.Insights from native mass spectrometry approaches for top- and middle- level characterization of site-specific antibody-drug conjugates.Site-selective incorporation and ligation of protein aldehydes.Designing sugar mimetics: non-natural pyranosides as innovative chemical tools.N-O linkage in carbohydrates and glycoconjugates.Piperidine-based glycodendrons as protein N-glycan prosthetics.Improving theranostics in pancreatic cancer.Engineered, highly reactive substrates of microbial transglutaminase enable protein labeling within various secondary structure elements.Mutation of Conserved Residues Increases in Vitro Activity of the Formylglycine-Generating Enzyme.Structural Basis for Copper-Oxygen Mediated C-H Bond Activation by the Formylglycine-Generating Enzyme.One-Step Derivatization of Reducing Oligosaccharides for Rapid and Live-Cell-Compatible Chelation-Assisted CuAAC Conjugation.In Vitro Reconstitution of Formylglycine-Generating Enzymes Requires Copper(I).Synthetic and semi-synthetic approaches to unprotected N-glycan oxazolines.
P2860
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P2860
Chemoenzymatic Fc glycosylation via engineered aldehyde tags.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
Chemoenzymatic Fc glycosylation via engineered aldehyde tags.
@en
Chemoenzymatic Fc glycosylation via engineered aldehyde tags.
@nl
type
label
Chemoenzymatic Fc glycosylation via engineered aldehyde tags.
@en
Chemoenzymatic Fc glycosylation via engineered aldehyde tags.
@nl
prefLabel
Chemoenzymatic Fc glycosylation via engineered aldehyde tags.
@en
Chemoenzymatic Fc glycosylation via engineered aldehyde tags.
@nl
P2093
P2860
P356
P1476
Chemoenzymatic Fc glycosylation via engineered aldehyde tags
@en
P2093
Anthony T Iavarone
Elizabeth L Smith
Kamil Godula
Lai-Xi Wang
P2860
P304
P356
10.1021/BC500061S
P577
2014-04-07T00:00:00Z