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Pregled bibliografske jedinice broj: 1279416

NIST interlaboratory study on glycosylation analysis of monoclonal antibodies: comparison of results from diverse analytical methods


De Leoz, Maria Lorna A.; Duewer, David L.; Fung, Adam; ...; Lauc, Gordan; ...; Leone, Joseph W.; Yuan, Hua; Stein, Stephen E.
NIST interlaboratory study on glycosylation analysis of monoclonal antibodies: comparison of results from diverse analytical methods // Molecular & cellular proteomics, 19 (2020), 1; 11-30 doi:10.1074/mcp.RA119.001677 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 1279416 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
NIST interlaboratory study on glycosylation analysis of monoclonal antibodies: comparison of results from diverse analytical methods

Autori
De Leoz, Maria Lorna A. ; Duewer, David L. ; Fung, Adam ; ... ; Lauc, Gordan ; ... ; Leone, Joseph W. ; Yuan, Hua ; Stein, Stephen E.

Izvornik
Molecular & cellular proteomics (1535-9476) 19 (2020), 1; 11-30

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
glycomics ; mass spectrometry ; fluorescence ; glycosylation ; glycoproteins ; glycan ; glycopeptide ; interlaboratory study ; NISTmAb ; reference antibody

Sažetak
Glycosylation is a topic of intense current interest in the development of biopharmaceuticals because it is related to drug safety and efficacy. This work describes results of an interlaboratory study on the glycosylation of the Primary Sample (PS) of NISTmAb, a monoclonal antibody reference material. Seventy-six laboratories from industry, university, research, government, and hospital sectors in Europe, North America, Asia, and Australia submitted a total of 103 reports on glycan distributions. The principal objective of this study was to report and compare results for the full range of analytical methods presently used in the glycosylation analysis of mAbs. Therefore, participation was unrestricted, with laboratories choosing their own measurement techniques. Protein glycosylation was determined in various ways, including at the level of intact mAb, protein fragments, glycopeptides, or released glycans, using a wide variety of methods for derivatization, separation, identification, and quantification. Consequently, the diversity of results was enormous, with the number of glycan compositions identified by each laboratory ranging from 4 to 48. In total, one hundred sixteen glycan compositions were reported, of which 57 compositions could be assigned consensus abundance values. These consensus medians provide community- derived values for NISTmAb PS. Agreement with the consensus medians did not depend on the specific method or laboratory type. The study provides a view of the current state-of-the-art for biologic glycosylation measurement and suggests a clear need for harmonization of glycosylation analysis methods.

Izvorni jezik
Engleski

Znanstvena područja
Temeljne medicinske znanosti



POVEZANOST RADA


Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb,
GENOS d.o.o.

Profili:

Avatar Url Gordan Lauc (autor)

Poveznice na cjeloviti tekst rada:

doi

Citiraj ovu publikaciju:

De Leoz, Maria Lorna A.; Duewer, David L.; Fung, Adam; ...; Lauc, Gordan; ...; Leone, Joseph W.; Yuan, Hua; Stein, Stephen E.
NIST interlaboratory study on glycosylation analysis of monoclonal antibodies: comparison of results from diverse analytical methods // Molecular & cellular proteomics, 19 (2020), 1; 11-30 doi:10.1074/mcp.RA119.001677 (međunarodna recenzija, članak, znanstveni)
De Leoz, M., Duewer, D., Fung, A., ..., Lauc, G., ..., Leone, J., Yuan, H. & Stein, S. (2020) NIST interlaboratory study on glycosylation analysis of monoclonal antibodies: comparison of results from diverse analytical methods. Molecular & cellular proteomics, 19 (1), 11-30 doi:10.1074/mcp.RA119.001677.
@article{article, author = {De Leoz, Maria Lorna A. and Duewer, David L. and Fung, Adam and Lauc, Gordan and Leone, Joseph W. and Yuan, Hua and Stein, Stephen E.}, year = {2020}, pages = {11-30}, DOI = {10.1074/mcp.RA119.001677}, keywords = {glycomics, mass spectrometry, fluorescence, glycosylation, glycoproteins, glycan, glycopeptide, interlaboratory study, NISTmAb, reference antibody}, journal = {Molecular and cellular proteomics}, doi = {10.1074/mcp.RA119.001677}, volume = {19}, number = {1}, issn = {1535-9476}, title = {NIST interlaboratory study on glycosylation analysis of monoclonal antibodies: comparison of results from diverse analytical methods}, keyword = {glycomics, mass spectrometry, fluorescence, glycosylation, glycoproteins, glycan, glycopeptide, interlaboratory study, NISTmAb, reference antibody} }
@article{article, author = {De Leoz, Maria Lorna A. and Duewer, David L. and Fung, Adam and Lauc, Gordan and Leone, Joseph W. and Yuan, Hua and Stein, Stephen E.}, year = {2020}, pages = {11-30}, DOI = {10.1074/mcp.RA119.001677}, keywords = {glycomics, mass spectrometry, fluorescence, glycosylation, glycoproteins, glycan, glycopeptide, interlaboratory study, NISTmAb, reference antibody}, journal = {Molecular and cellular proteomics}, doi = {10.1074/mcp.RA119.001677}, volume = {19}, number = {1}, issn = {1535-9476}, title = {NIST interlaboratory study on glycosylation analysis of monoclonal antibodies: comparison of results from diverse analytical methods}, keyword = {glycomics, mass spectrometry, fluorescence, glycosylation, glycoproteins, glycan, glycopeptide, interlaboratory study, NISTmAb, reference antibody} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


Citati:





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