Author

A. Jankevics

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· 3 Cancer Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Assay:proteomics· 3 Research Focus:protein folding & dynamics· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell type annotation· 1 Organism:human· 1 Organism:mouse· 1 Organism:multiple species· 1

Frequent Co-Authors

R. A. Scheltema· 3 shared A. J. R. Heck· 2 shared A. Cabrera-Orefice· 1 shared A. D. Southam· 1 shared A. F. L. Hurlstone· 1 shared A. P. Badrock· 1 shared A. Potter· 1 shared C. Ceol· 1 shared

Activity by Year

2020-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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3 shared papersBiochemistry

R. A. Scheltema

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Fast and accurate disulfide bridge detection

S. Heissel, Y. He, A. Jankevics, Y. Shi, H. Molina, R. Viner, R. A. Scheltema

This paper presents a fast and accurate method for detecting disulfide bridges in proteins using mass spectrometry with optimized sample preparation and data analysis.

bioRxiv · Nov 22, 2023Biochemistry

MRPS36 provides a missing link in the eukaryotic 2-oxoglutarate dehydrogenase complex for recruitment of E3 to the E2 core

J. f. Hevler, P. Albanese, A. Cabrera-Orefice, A. Potter, A. Jankevics, J. Misic, R. A. Scheltema, U. Brandt, S. Arnold, A. J. R. Heck

The paper identifies MRPS36 as an essential component of the eukaryotic 2-oxoglutarate dehydrogenase complex, replacing the bacterial PSBD and providing structural insights into its organization.

bioRxiv · Oct 8, 2022 · PreprintBiochemistry

Oxonium Ion-Guided Ion Mobility-Assisted Glycoproteomics on the timsTOF Pro

S. Mukherjee, A. Jankevics, F. Busch, M. Lubeck, Y. Zou, G. Kruppa, A. J. R. Heck, R. A. Scheltema, K. Reiding

This paper introduces a method using ion mobility on the timsTOF Pro to separate glycopeptides from non-modified peptides, improving glycoproteomics analysis of complex samples.

bioRxiv · Jul 4, 2022Biochemistry

DGAT1 is a lipid metabolism oncoprotein that enables cancer cells to accumulate fatty acid while avoiding lipotoxicity

D. J. Wilcock, A. P. Badrock, R. Owen, M. Guerin, A. D. Southam, H. Johnston, S. Ogden, P. Fullwood, J. Watson, H. Ferguson, J. Haworth, D. A. Richardson, G. R. Lloyd, A. Jankevics, W. B. Dunn, , A. F. L. Hurlstone

This study identifies DGAT1 as an oncoprotein that enables cancer cells to accumulate fatty acids while avoiding lipotoxicity, promoting melanoma formation.

bioRxiv · Jun 23, 2020 · PreprintCancer Biology