Weston B. Struwe

The Minimum Information Required for a Glycomics Experiment (MIRAGE) Project: Improving the Standards for Reporting Mass-spectrometry-based Glycoanalytic Data.

Increase in sialylation and branching in the mouse serum N-glycome correlates with inflammation and ovarian tumour progression.

MIRAGE: the minimum information required for a glycomics experiment.

Ejection of structural zinc leads to inhibition of γ-butyrobetaine hydroxylase.

Native mass spectrometry: towards high-throughput structural proteomics.

Studying the active-site loop movement of the São Paolo metallo-β-lactamase-1†Electronic supplementary information (ESI) available: Procedures for protein expression and purification, F-labelling, crystallisation, data collection, and structure determination, table of crystallographic data, table of crystallographic parameters and refinement statistics, figures showing binding mode and distances, procedures for mass spectrometry measurements, differential scanning fluorimetry measurements, stopped-flow measurements and other kinetics measurements. See DOI: 10.1039/c4sc01752hClick here for additional data file.

GlycoMob: an ion mobility-mass spectrometry collision cross section database for glycomics.

Structural characterization and biological implications of sulfated N-glycans in a serine protease from the neotropical moth Hylesia metabus (Cramer [1775]) (Lepidoptera: Saturniidae).

Optimal Synthetic Glycosylation of a Therapeutic Antibody.

High-resolution mass spectrometry of small molecules bound to membrane proteins.

Travelling-wave ion mobility and negative ion fragmentation of high-mannose N-glycans.

Composition and Antigenic Effects of Individual Glycan Sites of a Trimeric HIV-1 Envelope Glycoprotein.

Immune recruitment or suppression by glycan engineering of endogenous and therapeutic antibodies.

Structures of mammalian ER α-glucosidase II capture the binding modes of broad-spectrum iminosugar antivirals.

Travelling-wave ion mobility mass spectrometry and negative ion fragmentation of hybrid and complex N-glycans.

Optimal Synthetic Glycosylation of a Therapeutic Antibody.

Antibody production using a ciliate generates unusual antibody glycoforms displaying enhanced cell-killing activity.

The minimum information required for a glycomics experiment (MIRAGE) project: sample preparation guidelines for reliable reporting of glycomics datasets.

Ion mobility separation of deprotonated oligosaccharide isomers - evidence for gas-phase charge migration.

Molecular Architecture of the Cleavage-Dependent Mannose Patch on a Soluble HIV-1 Envelope Glycoprotein Trimer.

Global N-Glycan Site Occupancy of HIV-1 gp120 by Metabolic Engineering and High-Resolution Intact Mass Spectrometry.

The minimum information required for a glycomics experiment (MIRAGE) project: improving the standards for reporting glycan microarray-based data.

The role of interfacial lipids in stabilizing membrane protein oligomers.

Identification of Lewis and Blood Group Carbohydrate Epitopes by Ion Mobility-Tandem-Mass Spectrometry Fingerprinting.

The Tetrameric Plant Lectin BanLec Neutralizes HIV through Bidentate Binding to Specific Viral Glycans.

Glycan Fingerprinting via Cold-Ion Infrared Spectroscopy.

Reducing V3 Antigenicity and Immunogenicity on Soluble, Native-Like HIV-1 Env SOSIP Trimers.

Convergent immunological solutions to Argentine hemorrhagic fever virus neutralization.

Glycosylation profiling to evaluate glycoprotein immunogens against HIV-1.

Integrity of Glycosylation Processing of a Glycan-Depleted Trimeric HIV-1 Immunogen Targeting Key B-Cell Lineages.

Structural principles that enable oligomeric small heat-shock protein paralogs to evolve distinct functions.

Isomer Information from Ion Mobility Separation of High-Mannose Glycan Fragments.

Collision Cross Sections and Ion Mobility Separation of Fragment Ions from Complex N-Glycans.

Fucose Migration in Intact Protonated Glycan Ions: A Universal Phenomenon in Mass Spectrometry.

Quantitative mass imaging of single biological macromolecules.

Signature of Antibody Domain Exchange by Native Mass Spectrometry and Collision-Induced Unfolding.

Structural Studies of Fucosylated N-Glycans by Ion Mobility Mass Spectrometry and Collision-Induced Fragmentation of Negative Ions.

Structural Insights into the Broad-Spectrum Antiviral Target Endoplasmic Reticulum Alpha-Glucosidase II.

The Jumonji-C oxygenase JMJD7 catalyzes (3S)-lysyl hydroxylation of TRAFAC GTPases.

Publisher Correction: The Jumonji-C oxygenase JMJD7 catalyzes (3S)-lysyl hydroxylation of TRAFAC GTPases.

N-glycan microheterogeneity regulates interactions of plasma proteins.

Site-Specific Glycosylation of Virion-Derived HIV-1 Env Is Mimicked by a Soluble Trimeric Immunogen.

A Mass-Spectrometry-Based Modelling Workflow for Accurate Prediction of IgG Antibody Conformations in the Gas Phase.

The minimum information required for a glycomics experiment (MIRAGE) project: LC guidelines.

In-depth structural analysis of glycans in the gas phase.

Probing -glycoprotein microheterogeneity by lectin affinity purification-mass spectrometry analysis.

Separation of Isomeric Glycans by Ion Mobility and Liquid Chromatography-Mass Spectrometry.

Relating glycoprotein structural heterogeneity to function - insights from native mass spectrometry.

Towards a standardized bioinformatics infrastructure for N- and O-glycomics.

Separation of isomeric glycans by ion mobility spectrometry - the impact of fluorescent labelling.

Ion Mobility-Mass Spectrometry of Glycoconjugates.

A bipartite structural organization defines the SERINC family of HIV-1 restriction factors.

Quantifying Protein-Protein Interactions by Molecular Counting with Mass Photometry.

Shotgun ion mobility mass spectrometry sequencing of heparan sulfate saccharides.

Quantifying the heterogeneity of macromolecular machines by mass photometry.

Single molecule mass photometry of nucleic acids.

Hyper-truncated Asn355- and Asn391-glycans modulate the activity of neutrophil granule myeloperoxidase.

Correlating Glycoforms of DC-SIGN with Stability Using a Combination of Enzymatic Digestion and Ion Mobility Mass Spectrometry.

Mass Photometry of Membrane Proteins.

Assessing Antigen Structural Integrity through Glycosylation Analysis of the SARS-CoV-2 Viral Spike.

Native Mass Spectrometry Meets Glycomics: Resolving Structural Detail and Occupancy of Glycans on Intact Glycoproteins.

Identification of N-glycans with GalNAc-containing antennae from recombinant HIV trimers by ion mobility and negative ion fragmentation.

Label-free methods for optical characterization of protein-protein interactions.

Formation and fragmentation of doubly and triply charged ions in the negative ion spectra of neutral N-glycans from viral and other glycoproteins.

State-of-the-art glycosaminoglycan characterization.

Direct observation of the molecular mechanism underlying protein polymerization.

An N-glycan on the C2 domain of JAGGED1 is important for Notch activation.

Mass photometry reveals SARS-CoV-2 spike stabilisation to impede ACE2 binding through altered conformational dynamics.

Engineer RNA-Protein Nanowires as Light-Responsive Biomaterials.

Uncovering the Role of -Glycan Occupancy on the Cooperative Assembly of Spike and Angiotensin Converting Enzyme 2 Complexes: Insights from Glycoengineering and Native Mass Spectrometry.

Measuring Protein-Protein Interactions and Quantifying Their Dissociation Constants with Mass Photometry.