Author

M. Meier-Schellersheim

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

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:deep learning· 2 Research Focus:host-pathogen & immune response· 2 Organism:human· 2 Assay:proteomics· 2 Approach:statistical model· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1

Frequent Co-Authors

C. T. Boughter· 3 shared A. Nita-Lazar· 1 shared B. Marrero· 1 shared C. J. Bradfield· 1 shared H. Bongartz· 1 shared I. Fraser· 1 shared J. L. Gross· 1 shared R. A. Gottschalk· 1 shared

Activity by Year

2022-2024 · peak 2/yr

Co-Author Collaboration Network

9 top collaborators · 36 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersImmunology

C. T. Boughter

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Macrophages tune responses to pathogen dynamics through TLR4 stimulation memory and by licensing susceptibility to IL-10

H. Bongartz, C. T. Boughter, B. Marrero, T. Prustel, C. J. Bradfield, J. L. Gross, R. A. Gottschalk, A. Nita-Lazar, I. Fraser, M. Meier-Schellersheim

The paper shows macrophages use TLR4 memory and IL-10 susceptibility gating to adjust inflammation based on pathogen dynamics.

bioRxiv · Mar 28, 2024 · PreprintImmunology

An Integrated Approach to the Characterization of Immune Repertoires Using AIMS: An Automated Immune Molecule Separator

C. T. Boughter, M. Meier-Schellersheim

The paper introduces AIMS, a software tool for integrated analysis of immune repertoire data, enabling comparison across TCR, MHC, peptide, antibody, and antigen sequences to identify interaction hotspots.

bioRxiv · Dec 7, 2022Immunology

Conserved Biophysical Compatibility Among the Highly Variable Germline-Encoded Regions Shapes TCR-MHC Interactions

C. T. Boughter, M. Meier-Schellersheim

The paper analyzes all possible germline-encoded TCR-MHC contacts in humans, showing that conserved interactions are rare and that biophysical compatibility, not sequence conservation, defines binding orientation.

bioRxiv · Dec 7, 2022Immunology