Author

F. Meier

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Biochemistry· 6 Biophysics· 1 Pathology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 6 Assay:proteomics· 6 Organism:human· 4 Research Focus:protein folding & dynamics· 4 Research Focus:benchmarking· 2 Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Research Focus:protein structure prediction· 2

Frequent Co-Authors

M. Mann· 5 shared M. Thielert· 2 shared P. E. Geyer· 2 shared P. Skowronek· 2 shared S. Willems· 2 shared A. Applebaum· 1 shared A. K. Okada· 1 shared A. Krag· 1 shared

Activity by Year

2017-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 15 mutual co-author links

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5 shared papersBiochemistry

M. Mann

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Author profile →

8 papers

Recent·Most cited

EXCRETE enables deep proteomics of the microbial extracellular environment

D. A. Russo, D. Oliinyk, G. Pohnert, F. Meier, J. A. Z. Zedler

EXCRETE improves exoproteome identification in cyanobacteria, revealing 85% of predicted secreted proteins and highlighting key functions in cell envelope maintenance and nutrient acquisition.

bioRxiv · Mar 1, 2024 · PreprintBiochemistry

Synchro-PASEF allows precursor-specific fragment ion extraction and interference removal in data-independent acquisition

P. Skowronek, F. Krohs, M. Lubeck, G. Wallmann, E. Itang, P. Koval, M. Wahle, M. Thielert, F. Meier, S. Willems, O. Raether, M. Mann

This paper introduces synchro-PASEF, a method that improves fragment ion extraction and interference removal in DIA proteomics by synchronizing ion mobility and mass dimensions.

bioRxiv · Nov 1, 2022Biochemistry

Rapid and in-depth coverage of the (phospho-)proteome with deep libraries and optimal window design for dia-PASEF

P. Skowronek, M. Thielert, E. Voytik, M. C. Tanzer, F. M. Hansen, S. Willems, O. Karayel, A.-D. Brunner, F. Meier, M. Mann

This paper introduces an optimized dia-PASEF method with variable isolation windows to enhance proteome and phosphoproteome coverage in mass spectrometry.

bioRxiv · May 31, 2022Biochemistry

A paired liver biopsy and plasma proteomics study reveals circulating biomarkers for alcohol-related liver disease

L. Niu, M. Thiele, P. E. Geyer, D. N. Rasmussen, H. E. Webel, A. Santos, R. Gupta, F. Meier, M. Strauss, M. Kjaergaard, K. Lindvig, S. Jacobsen, S. Rasmussen, T. Hansen, A. Krag, M. Mann

This study identifies circulating proteomic biomarkers for alcohol-related liver disease using paired liver biopsy and plasma proteomics, showing improved performance over existing tests.

bioRxiv · Oct 16, 2020 · PreprintBiochemistry

Ectopic bone formation and systemic bone loss in a transmembrane TNF-driven model of human spondyloarthritis

E. Christodoulou-Vafeiadou, C. Geka, L. Ntari, K. Kranidioti, E. Argyropoulou, F. Meier, M. Armaka, I. Mourouzis, C. Pantos, M. Rouchota, G. Loudos, M. C. Denis, N. Karagianni, G. Kollias

This paper characterizes a transmembrane TNF-driven mouse model of spondyloarthritis, showing ectopic bone formation, systemic bone loss, and comorbid heart valve pathology, with early anti-TNF treatment reducing inflammation.

bioRxiv · May 14, 2020Pathology

Huntingtin fibrils with different toxicity, structure, and seeding potential can be reversibly interconverted

J. M. Isas, N. K. Pandey, K. Teranishi, A. K. Okada, A. Applebaum, F. Meier, R. Langen, A. Siemer

This study shows that HTTex1 fibrils with different toxicity and structure can be reversibly interconverted through changes in C-terminal domain dynamics.

bioRxiv · Jul 16, 2019 · PreprintBiophysics

A novel LC system embeds analytes in pre-formed gradients for rapid, ultra-robust proteomics

N. Bache, P. E. Geyer, D. B. Bekker-Jensen, O. Hoerning, L. Falkenby, P. V. Treit, S. Doll, I. Paron, F. Meier, J. V. Olsen, O. Vorm, M. Mann

The paper introduces a novel LC system for proteomics that enables rapid, high-throughput, and robust analysis with deep proteome coverage.

bioRxiv · May 15, 2018Biochemistry

EASI-tag enables accurate multiplexed and interference-free MS2-based proteome quantification

S. Virreira Winter, F. Meier, C. Wichmann, J. Cox, M. Mann, F. Meissner

EASI-tag enables accurate multiplexed proteome quantification by generating interference-free reporter ions through dissociation at low collision energy.

bioRxiv · Nov 27, 2017Biochemistry