Applications of targeted proteomics in systems biology and translational medicine
Open accessAbstract
Biological systems are composed of numerous components of which proteins are of particularly high functional significance. Network models are useful abstractions for studying these components in context. Network representations display molecules as nodes and their interactions as edges. Because they are difficult to directly measure, functional edges are frequently inferred from suitably structured datasets consisting of the accurate and consistent quantification of network nodes under a multitude of perturbed conditions. For the precise quantification of a finite list of proteins across a wide range of samples, targeted proteomics exemplified by selected/multiple reaction monitoring (SRM, MRM) mass spectrometry has proven useful and has been applied to a variety of questions in systems biology and clinical studies. Here, we survey the literature of studies using SRM‐MS in systems biology and clinical proteomics. Systems biology studies frequently examine fundamental questions in network biology, whereas clinical studies frequently focus on biomarker discovery and validation in a variety of diseases including cardiovascular disease and cancer. Targeted proteomics promises to advance our understanding of biological networks and the phenotypic significance of specific network states and to advance biomarkers into clinical use.
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Targeted MS technologies such as SRM/MRM and PRM offer a promising alternative to the challenges of immunoassay validation.
“As an antibody-free platform with robust sensitivity, high accuracy, and an exceptional multiplex capacity, targeted MS technologies such as SRM/MRM and PRM offer a promising alternative to the challenges of immunoassay validation [184–187].”
From Systems-based proteomics to resolve the biology of Alzheimer’s disease beyond amyloid and tau (2021) · cites this paper as [185]
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- Authors
- Ebhardt, H. A., Root, A., Sander, C., & Aebersold, R.
- Affiliations
- ETH Zurich (CH)
- Memorial Sloan Kettering Cancer Center (US)
- University of Zurich (CH)
- Corresponding author
- Ebhardt, H. Alexander
- Venue
- PROTEOMICS
- Publisher
- Wiley
- Published
- 2015-07-16
- Volume
- 15
- Issue
- 18
- Pages
- 3193-3208
- ISSN
- 1615-9853 (ISSN-L)
- 1615-9861
- PMC
- PMC4758406
- OpenAlex
- W2164522178
- Cited by
- 184
- References
- 141
- Citations by year
- 2026: 4 · 2025: 6 · 2024: 10 · 2023: 14 · 2022: 12 · 2021: 18 · 2020: 15 · 2019: 25 · 2018: 22 · 2017: 24 · 2016: 32 · 2015: 2
- FWCI
- 2.58
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- PROTEOMICS (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- SystemsX.ch project PhosphoNetX
- SNSF (3100A0-688 107679)
- European Research Council (ERC-2008-AdG 233226)
- Topics
- Physical Sciences › Chemistry › Spectroscopy › Advanced Proteomics Techniques and Applications
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Advanced Biosensing Techniques and Applications
- Keywords
- targeted proteomics, multiple reaction monitoring, systems biology, network biology, biomarker discovery, biomarker validation, clinical proteomics, protein quantification, cardiovascular disease, cancer
- MeSH terms
- Humans, Proteomics, Systems Biology, Translational Research, Biomedical
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