Author

Greta Šneiderienė

University of CambridgeORCID 0000-0002-4585-5091Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Biochemistry· 1 Biophysics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:host-pathogen & immune response· 2 Assay:proteomics· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:differential expression· 1 Organism:human· 1

Frequent Co-Authors

Sara Snogerup LinseiD· 2 shared Tuomas P. J. KnowlesiD· 2 shared Alexander J. DeariD· 1 shared Alicia González DíaziD· 1 shared Dev ThackeriD· 1 shared Elin StemmeiD· 1 shared Ewa A. AndrzejewskaiD· 1 shared Gunnar K. GourasiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersBiochemistry

Sara Snogerup LinseORCID

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2 papers

Recent·Most cited

BiochemistrybioRxivPreprintJul 31, 2026

Errors in peptide synthesis are a source of discrepancies in Aβ42 studies

Karolina Matulewska-Sobczuk, Katja Bernfur, Dev Thacker…·Lei Ortigosa-Pascual

This study shows that sequence imperfections in synthetic Aβ42 peptides cause differences in aggregation behavior compared to recombinant Aβ42.

DOI 10.64898/2026.07.30.741826

proteomicsexperimental assay

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BiophysicsProceedings of the National Academy of SciencesPeer-reviewedJan 24, 2025

The Alzheimer's Amyloid beta peptide forms biomolecular condensates that trigger amyloid aggregation

Greta Šneiderienė, Alicia González Díaz, Sourav Dasadhikari…·Tuomas P. J. Knowles

This paper shows that Alzheimer's amyloid-beta peptide forms biomolecular condensates on lipid bilayers, accelerating amyloid aggregation and revealing a new early step in the disease mechanism.

41 citationstop 1%

humanproteomics

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