Immobilized hdx

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Aerococcus urinae NBRC 15544 = CCUG 36881 (187)
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pride (187)
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iBET – Instituto de Biologia Experimental e Tecnológica, Av. da República, Oeiras, 2780-157, Portugal (14)
School of Pharmacy, Sungkyunkwan University, South Korea (5)
Department of Chemistry & Chemical Biology, Northeastern University (4)
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Protein Analysis Group, Department of Pharmacy, University of Copenhagen, Copenhagen, Denmark (3)
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Kobilka Institute of Innovative Drug Discovery, School ofMedicine, The Chinese University of Hong Kong, Shenzhen, China, 518172 (2)
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University of Edinburgh, Institute of Genetics and Molecular Medicine, Edinburgh, Scotland, United Kingdom, EH4 2XR (2)
University of Geneva, Department of Microbiology and Molecular Medicine (2)
Zhejiang University (2)
1 Max Planck Fellow Group Molecular Physiology of Microbes, Max Planck Institute for Terrestrial Microbiology, Marburg, Germany 2 Center for Synthetic Microbiology (SYNMIKRO), Marburg, Germany 3 Department of Chemistry, University of Marburg, Marburg, Germany (1)
1 Max-Planck Institute for Terrestrial Microbiology, Karl-von-Frisch Strasse 14, 35043 Marburg, Germany 2 University of Marburg, Center for Synthetic Microbiology (SYNMIKRO) & Departments of Chemistry and Biology, Karl-von-Frisch Strasse 14, 35043 Marburg, Germany (1)
Biological NMR and HDX-MS Platform, Institut Pasteur, Université Paris Cité, CNRS UMR 3528, 75015 Paris, France (1)
Center for Synthetic Microbiology & Department of Chemistry, Marburg University,Hans-Meerwein-Straße 4, 35043 Marburg, Germany (1)
Center for Synthetic Microbiology (SYNMIKRO) & Department of Chemistry, Philipps-University Marburg, Marburg, Germany (1)
Center for Synthetic Microbiology (SYNMIKRO) & Faculty of Chemistry, Philipps-University Marburg, 35043 Marburg, Germany (1)
Chromatin Structure & Mobile DNA Laboratory, The Francis Crick Institute, London, NW1 1AT, UK. (1)
Department of Biochemistry University of Washington, Seattle (1)
Department of Biochemistry and Microbiology, University of Victoria, BC, Canada (1)
Department of Biochemistry and Molecular Biology, Pennsylvania State University (1)
Department of Biochemistry and Molecular Biology, Section for Biomedical Mass Spectrometry and Systems Biology, University of Southern Denmark (1)
Department of Biochemistry and Pharmacology, University of Melbourne, Parkville, VIC 3010, Australia (1)

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HDX-MS of Immobilized Staph Enterotoxin B with Neutralizing Serum

Elucidating the interactions that drive antigen recognition is central to understanding antibody-based protection and is vital for the rational design of immunogens. Often, structural knowledge of epitopes targeted by antibodies is derived from isolated studies of monoclonal antibodies, for which nu...

ORGANISM(S): Mus musculus (Mouse)

2025-10-27 | PXD051156 | Pride

Hydrogen deuterium exchange epitope mapping of glycosylated epitopes enabled by online immobilized glycosidase

Numerous mAbs are known to recognize N-glycosylated epitopes or to bind in close proximity to an N-glycan site, however, glycosylated protein sites are typically obscured from HDX detection as a result of the inherent heterogeneity of glycans. To overcome this limitation, we covalently immobilized ...

ORGANISM(S): Homo sapiens (Human)

2024-05-24 | PXD041204 | Pride

Lc/ms-ms Hdx

Epitope Mapping of Human Polyclonal Antibodies to the fHbp Antigen of a Neisseria Meningitidis Vaccine by Hydrogen-Deuterium Exchange Mass Spectrometry (HDX-MS) - part 2

Antigen-antibody interactions play a key role in the immune response post vaccination and the mechanism of action of antibody-based biopharmaceuticals. 4CMenB is a multicomponent vaccine against Neisseria meningitidis serogroup B in which factor H binding protein (fHbp) is one of the key antigens. I...

ORGANISM(S): Homo sapiens (Human)

2024-05-22 | PXD047712 | Pride

Pab Fhbp Hdx-ms

Epitope Mapping of Human Polyclonal Antibodies to the fHbp Antigen of a Neisseria Meningitidis Vaccine by Hydrogen-Deuterium Exchange Mass Spectrometry (HDX-MS)

ORGANISM(S): Homo sapiens (Human)

2024-05-24 | PXD046572 | Pride

Polyclonal antibodies Pab Fhbp Hdx-ms

An HDX-MS optimised approach to characterise nanobodies as tools for biochemical and structural studies

Given the far-reaching applications of nanobodies, a stream-lined approach to characterizing nanobodies tailored to its intended application is warranted. Camelids can produce a large number of antibodies that can bind to a host of epitopes spanning the entire protein of interest, making identificat...

ORGANISM(S): Homo sapiens (Human)

2021-09-22 | PXD025207 | Pride

Hdx-ms Pi3k Nanobody

RSV nonstructural protein 1 (NS1) HDX LC-MS data

Raw liquid chromatography-mass spectrometry (LC-MS) datafiles acquired for hydrogen-deuterium exchange (HDX) of RSV nonstructural protein 1 (NS1)

ORGANISM(S): Human Respiratory syncytial virus 9320

2025-05-07 | PXD054005 | Pride

Rsv ns1 hdx-ms

HDX of SEB and Neutralizing mAbs

ORGANISM(S): Mus musculus (Mouse)

2025-10-27 | PXD051141 | Pride

Hdx-ms Hydorgen deuterium exchange Seb

Epitope analysis of the complex of CD73 and HB0038 by HDX-MS

Epitope analysis of the complex of CD73 antigen and the anti-CD73 antibody HB0038 by HDX-MS

ORGANISM(S): Homo sapiens (Human)

2025-05-07 | PXD057867 | Pride

Cd73 hb0038 hdx-ms

Human Calcitonin and Amylin receptor HDX-MS

Receptor activity-modifying proteins (RAMPs) regulate the pharmacology, trafficking, and signaling of class B1 G protein-coupled receptors (GPCRs). The calcitonin receptor (CTR) interacts with each of the three RAMPs to form amylin receptors (AMYRs), which display distinct ligand preferences and sig...

ORGANISM(S): Homo sapiens (Human)

2026-06-08 | PXD068848 | Pride

Calcitonin recepto Hdx-ms Recepror activity modifying protein (ramp) Gpcr Amylin receptor

HDX-MS analysis of the mechanism of AKT1 inhibitor binding

Analysis of AKT1 inhibitor binding using HDX-MS .

ORGANISM(S): Homo sapiens (Human)

2023-02-22 | PXD032929 | Pride

Hdx-ms Akt1 Akt drlink Akt da

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