Evidence map›Paper›PMID 33284343›Full record

ArticleThe Biochemical journal2021

Hydrogen deuterium exchange mass spectrometry identifies the dominant paratope in CD20 antigen binding to the NCD1.2 monoclonal antibody.

Lukas Uhrik, Lenka Hernychova, Petr Muller, Umesh Kalathiya, Malgorzata M Lisowska, Mikolaj Kocikowski, Maciej Parys, Jakub Faktor, Marta Nekulova, Chris Nortcliffe and 7 more

Open access · hybridAbstract read
In one paragraph

Article in The Biochemical journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 6 institutions in 6 countries.

Lukas UhrikResearch Centre for Applied Molecular Oncology, Masaryk Memorial Cancer Institute, Zluty kopec 7, 656 53 Brno, Czech Republic.
Lenka HernychovaResearch Centre for Applied Molecular Oncology, Masaryk Memorial Cancer Institute, Zluty kopec 7, 656 53 Brno, Czech Republic.
Petr MullerResearch Centre for Applied Molecular Oncology, Masaryk Memorial Cancer Institute, Zluty kopec 7, 656 53 Brno, Czech Republic.
Umesh KalathiyaInternational Centre for Cancer Vaccine Science, University of Gdansk, ul. Kładki 24 80-822 Gdańsk, Poland.
Malgorzata M LisowskaInternational Centre for Cancer Vaccine Science, University of Gdansk, ul. Kładki 24 80-822 Gdańsk, Poland.
Mikolaj KocikowskiInternational Centre for Cancer Vaccine Science, University of Gdansk, ul. Kładki 24 80-822 Gdańsk, Poland.
Maciej ParysInstitute of Genetics and Molecular Medicine, University of Edinburgh, EH4 2XR Edinburgh, U.K.
Jakub FaktorInternational Centre for Cancer Vaccine Science, University of Gdansk, ul. Kładki 24 80-822 Gdańsk, Poland.
Marta NekulovaResearch Centre for Applied Molecular Oncology, Masaryk Memorial Cancer Institute, Zluty kopec 7, 656 53 Brno, Czech Republic.
Chris NortcliffeSciex, Phoenix House Lakeside Drive Centre Park WA1 1RX, Warrington, U.K.
Pavlina ZatloukalovaResearch Centre for Applied Molecular Oncology, Masaryk Memorial Cancer Institute, Zluty kopec 7, 656 53 Brno, Czech Republic.
Barbara RuetgenClinical Pathology, Department of Pathobiology, University of Veterinary Medicine Vienna, Veterinärplatz 1, 1210 Vienna, Austria.
Robin FahraeusResearch Centre for Applied Molecular Oncology, Masaryk Memorial Cancer Institute, Zluty kopec 7, 656 53 Brno, Czech Republic.
Kathryn L BallInstitute of Genetics and Molecular Medicine, University of Edinburgh, EH4 2XR Edinburgh, U.K.
David J ArgyleInstitute of Genetics and Molecular Medicine, University of Edinburgh, EH4 2XR Edinburgh, U.K.
Borivoj VojtesekResearch Centre for Applied Molecular Oncology, Masaryk Memorial Cancer Institute, Zluty kopec 7, 656 53 Brno, Czech Republic.
Ted R HuppResearch Centre for Applied Molecular Oncology, Masaryk Memorial Cancer Institute, Zluty kopec 7, 656 53 Brno, Czech Republic.
Masaryk Memorial Cancer Institute · CZEdinburgh Cancer Research · GBUniversity of Gdańsk · PLInserm · FRPhoenix Houses of New England · USUniversity of Veterinary Medicine Vienna · AT

Funding

Biotechnology and Biological Sciences Research Council BB/J00751X/1Biotechnology and Biological Sciences Research Council BB/R012385/1Biotechnology and Biological Sciences Research Council IAA PIII-024Biotechnology and Biological Sciences Research Council IAA, TEC3706
6 · The paper itself

Abstract

A comparative canine-human therapeutics model is being developed in B-cell lymphoma through the generation of a hybridoma cell that produces a murine monoclonal antibody specific for canine CD20. The hybridoma cell produces two light chains, light chain-3, and light chain-7. However, the contribution of either light chain to the authentic full-length hybridoma derived IgG is undefined. Mass spectrometry was used to identify only one of the two light chains, light chain-7, as predominating in the full-length IgG. Gene synthesis created a recombinant murine-canine chimeric monoclonal antibody expressing light chain-7 that reconstituted the IgG binding to CD20. Using light chain-7 as a reference sequence, hydrogen deuterium exchange mass spectrometry was used to identify the dominant CDR region implicated in CD20 antigen binding. Early in the deuteration reaction, the CD20 antigen suppressed deuteration at CDR3 (VH). In later time points, deuterium suppression occurred at CDR2 (VH) and CDR2 (VL), with the maintenance of the CDR3 (VH) interaction. These data suggest that CDR3 (VH) functions as the dominant antigen docking motif and that antibody aggregation is induced at later time points after antigen binding. These approaches define a methodology for fine mapping of CDR contacts using nested enzymatic reactions and hydrogen deuterium exchange mass spectrometry. These data support the further development of an engineered, synthetic canine-murine monoclonal antibody, focused on CDR3 (VH), for use as a canine lymphoma therapeutic that mimics the human-murine chimeric anti-CD20 antibody Rituximab.

Indexed as

Hydrogen Deuterium Exchange-Mass SpectrometryAmino Acid SequenceAnimalsAntibodies, MonoclonalAntigens, CD20Binding Sites, AntibodyCell Line, TumorChromatography, LiquidDogsHumansImmunoglobulin GImmunoglobulin Heavy ChainsImmunoglobulin Light ChainsKineticsPeptide LibraryRecombinant Fusion ProteinsAntibodies, MonoclonalAntigens, CD20Immunoglobulin GImmunoglobulin Heavy ChainsImmunoglobulin Light ChainsPeptide LibraryRecombinant Fusion ProteinsCD20comparative medicinehydrogen deuterium exchange mass spectrometrylymphomamonoclonal antibody

Identifiers

PMID33284343
PMCPMC7813475
OpenAlexW3113313372

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.