Effective protein extraction combined with data independent acquisition analysis reveals a comprehensive and quantifiable insight into the proteomes of articular cartilage and subchondral bone

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Effective protein extraction combined with data independent acquisition analysis reveals a comprehensive and quantifiable insight into the proteomes of articular cartilage and subchondral bone. / Bundgaard, L.; Åhrman, E.; Malmström, J.; auf dem Keller, U.; Walters, M.; Jacobsen, S.

I: Osteoarthritis and Cartilage, Bind 30, Nr. 1, 2022, s. 137-146.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Bundgaard, L, Åhrman, E, Malmström, J, auf dem Keller, U, Walters, M & Jacobsen, S 2022, 'Effective protein extraction combined with data independent acquisition analysis reveals a comprehensive and quantifiable insight into the proteomes of articular cartilage and subchondral bone', Osteoarthritis and Cartilage, bind 30, nr. 1, s. 137-146. https://doi.org/10.1016/j.joca.2021.09.006

APA

Bundgaard, L., Åhrman, E., Malmström, J., auf dem Keller, U., Walters, M., & Jacobsen, S. (2022). Effective protein extraction combined with data independent acquisition analysis reveals a comprehensive and quantifiable insight into the proteomes of articular cartilage and subchondral bone. Osteoarthritis and Cartilage, 30(1), 137-146. https://doi.org/10.1016/j.joca.2021.09.006

Vancouver

Bundgaard L, Åhrman E, Malmström J, auf dem Keller U, Walters M, Jacobsen S. Effective protein extraction combined with data independent acquisition analysis reveals a comprehensive and quantifiable insight into the proteomes of articular cartilage and subchondral bone. Osteoarthritis and Cartilage. 2022;30(1):137-146. https://doi.org/10.1016/j.joca.2021.09.006

Author

Bundgaard, L. ; Åhrman, E. ; Malmström, J. ; auf dem Keller, U. ; Walters, M. ; Jacobsen, S. / Effective protein extraction combined with data independent acquisition analysis reveals a comprehensive and quantifiable insight into the proteomes of articular cartilage and subchondral bone. I: Osteoarthritis and Cartilage. 2022 ; Bind 30, Nr. 1. s. 137-146.

Bibtex

@article{ae91fdcd0b3f440493ce196fc32944d9,
title = "Effective protein extraction combined with data independent acquisition analysis reveals a comprehensive and quantifiable insight into the proteomes of articular cartilage and subchondral bone",
abstract = "Objective: The objectives of this study was to establish a sensitive and reproducible method to map the cartilage and subchondral bone proteomes in quantitative terms, and mine the proteomes for proteins of particular interest in the pathogenesis of osteoarthritis (OA). The horse was used as a model animal. Design: Protein was extracted from articular cartilage and subchondral bone samples from three horses in triplicate by pressure cycling technology or ultrasonication. Digested proteins were analysed by data independent acquisition based mass spectrometry. Data was processed using a pre-established spectral library as reference database (FDR 1%). Results: We identified to our knowledge the hitherto most comprehensive quantitative cartilage (1758 proteins) and subchondral bone (1482 proteins) proteomes in all species presented to date. Both extraction methods were sensitive and reproducible and the high consistency of the identified proteomes (>97% overlap) indicated that both methods preserved the diversity among the extracted proteins. Proteome mining revealed a substantial number of quantifiable cartilage and bone matrix proteins and proteins involved in osteogenesis and bone remodeling, including ACAN, BGN, PRELP, FMOD, COMP, ACP5, BMP3, BMP6, BGLAP, TGFB1, IGF1, ALP, MMP3, and collagens. A number of proteins, including COMP and TNN, were identified in different protein isoforms with potential unique biological roles. Conclusion: We have successfully developed two sensitive and reproducible non-species specific workflows enabling a comprehensive quantitative insight into the proteomes of cartilage and subchondral bone. This facilitates the prospect of investigating the molecular events at the osteochondral unit in the pathogenesis of OA in future projects.",
keywords = "Cartilage, Data independent acquisition, Horse, Osteoarthritis, Proteome, Subchondral bone",
author = "L. Bundgaard and E. {\AA}hrman and J. Malmstr{\"o}m and {auf dem Keller}, U. and M. Walters and S. Jacobsen",
note = "Publisher Copyright: {\textcopyright} 2021 Osteoarthritis Research Society International",
year = "2022",
doi = "10.1016/j.joca.2021.09.006",
language = "English",
volume = "30",
pages = "137--146",
journal = "Osteoarthritis and Cartilage",
issn = "1063-4584",
publisher = "Elsevier",
number = "1",

}

RIS

TY - JOUR

T1 - Effective protein extraction combined with data independent acquisition analysis reveals a comprehensive and quantifiable insight into the proteomes of articular cartilage and subchondral bone

AU - Bundgaard, L.

AU - Åhrman, E.

AU - Malmström, J.

AU - auf dem Keller, U.

AU - Walters, M.

AU - Jacobsen, S.

N1 - Publisher Copyright: © 2021 Osteoarthritis Research Society International

PY - 2022

Y1 - 2022

N2 - Objective: The objectives of this study was to establish a sensitive and reproducible method to map the cartilage and subchondral bone proteomes in quantitative terms, and mine the proteomes for proteins of particular interest in the pathogenesis of osteoarthritis (OA). The horse was used as a model animal. Design: Protein was extracted from articular cartilage and subchondral bone samples from three horses in triplicate by pressure cycling technology or ultrasonication. Digested proteins were analysed by data independent acquisition based mass spectrometry. Data was processed using a pre-established spectral library as reference database (FDR 1%). Results: We identified to our knowledge the hitherto most comprehensive quantitative cartilage (1758 proteins) and subchondral bone (1482 proteins) proteomes in all species presented to date. Both extraction methods were sensitive and reproducible and the high consistency of the identified proteomes (>97% overlap) indicated that both methods preserved the diversity among the extracted proteins. Proteome mining revealed a substantial number of quantifiable cartilage and bone matrix proteins and proteins involved in osteogenesis and bone remodeling, including ACAN, BGN, PRELP, FMOD, COMP, ACP5, BMP3, BMP6, BGLAP, TGFB1, IGF1, ALP, MMP3, and collagens. A number of proteins, including COMP and TNN, were identified in different protein isoforms with potential unique biological roles. Conclusion: We have successfully developed two sensitive and reproducible non-species specific workflows enabling a comprehensive quantitative insight into the proteomes of cartilage and subchondral bone. This facilitates the prospect of investigating the molecular events at the osteochondral unit in the pathogenesis of OA in future projects.

AB - Objective: The objectives of this study was to establish a sensitive and reproducible method to map the cartilage and subchondral bone proteomes in quantitative terms, and mine the proteomes for proteins of particular interest in the pathogenesis of osteoarthritis (OA). The horse was used as a model animal. Design: Protein was extracted from articular cartilage and subchondral bone samples from three horses in triplicate by pressure cycling technology or ultrasonication. Digested proteins were analysed by data independent acquisition based mass spectrometry. Data was processed using a pre-established spectral library as reference database (FDR 1%). Results: We identified to our knowledge the hitherto most comprehensive quantitative cartilage (1758 proteins) and subchondral bone (1482 proteins) proteomes in all species presented to date. Both extraction methods were sensitive and reproducible and the high consistency of the identified proteomes (>97% overlap) indicated that both methods preserved the diversity among the extracted proteins. Proteome mining revealed a substantial number of quantifiable cartilage and bone matrix proteins and proteins involved in osteogenesis and bone remodeling, including ACAN, BGN, PRELP, FMOD, COMP, ACP5, BMP3, BMP6, BGLAP, TGFB1, IGF1, ALP, MMP3, and collagens. A number of proteins, including COMP and TNN, were identified in different protein isoforms with potential unique biological roles. Conclusion: We have successfully developed two sensitive and reproducible non-species specific workflows enabling a comprehensive quantitative insight into the proteomes of cartilage and subchondral bone. This facilitates the prospect of investigating the molecular events at the osteochondral unit in the pathogenesis of OA in future projects.

KW - Cartilage

KW - Data independent acquisition

KW - Horse

KW - Osteoarthritis

KW - Proteome

KW - Subchondral bone

U2 - 10.1016/j.joca.2021.09.006

DO - 10.1016/j.joca.2021.09.006

M3 - Journal article

C2 - 34547431

AN - SCOPUS:85116723412

VL - 30

SP - 137

EP - 146

JO - Osteoarthritis and Cartilage

JF - Osteoarthritis and Cartilage

SN - 1063-4584

IS - 1

ER -

ID: 284197639