Author

A. Kiyatkin

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· 1 Biophysics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Assay:fluorescence / live-cell microscopy· 1 Organism:human· 1 Approach:microscopy & imaging analysis· 1 Research Focus:protein folding & dynamics· 1 Assay:protein structure· 1

Frequent Co-Authors

C. Hu· 2 shared M. A. Lemmon· 2 shared C. A. Leche· 1 shared D. J. Schodt· 1 shared D. Lidke· 1 shared E. A. Burns· 1 shared E. M. Mangiacapre· 1 shared H. R. Ortiz· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersBiophysics

C. Hu

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2 papers

Recent·Most cited

Distinct interactions stabilize EGFR dimers and higher-order oligomers in cell membranes

K. C. Mudumbi, E. A. Burns, D. J. Schodt, Z. O. Petrova, A. Kiyatkin, L. W. Kim, E. M. Mangiacapre, I. Ortiz-Caraveo, H. R. Ortiz, C. Hu, K. D. Ashtekar, K. A. Lidke, D. Lidke, M. A. Lemmon

This study investigates how EGFR dimers and higher-order oligomers form and interact in cell membranes using SPT and FRET, revealing the role of the tyrosine kinase domain in oligomerization.

bioRxiv · Apr 10, 2023Biophysics

Glioblastoma mutations impair ligand discrimination by EGFR

C. Hu, C. A. Leche, A. Kiyatkin, S. E. Stayrook, K. M. Ferguson, M. A. Lemmon

This study shows that GBM mutations in EGFR disrupt ligand discrimination by altering dimer structure and stability, leading to aberrant signaling.

bioRxiv · May 4, 2021 · PreprintBiochemistry