Author

A. Cattaneo

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 Evolutionary Biology· 1 Immunology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:protein folding & dynamics· 3 Assay:proteomics· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell type annotation· 1 Research Focus:clustering· 1 Approach:deep learning· 1 Organism:human· 1

Frequent Co-Authors

A. Pastore· 2 shared A. Bachi· 1 shared A. Benito-Martinez· 1 shared A. Kuzmanic· 1 shared A. Pierson· 1 shared A. S. Arseniev· 1 shared B. Gaudineau· 1 shared D. Lamba· 1 shared

Activity by Year

2018-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 12 mutual co-author links

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2 shared papersEvolutionary Biology

A. Pastore

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Author profile →

4 papers

Recent·Most cited

Structural Basis for the transmembrane signaling and antidepressant-induced activation of the receptor tyrosine kinase TrkB

E. F. Kot, S. A. Goncharuk, M. L. Franco, A. S. Arseniev, A. Benito-Martinez, M. Costa, A. Cattaneo, M. Vilar, K. S. Mineev

This study determines the structure of the TrkB transmembrane domain using NMR and shows how fluoxetine activates the receptor by binding to it.

bioRxiv · Jun 6, 2023Biochemistry

Protein structure without structure determination: direct coupling analysis based on in vitro evolution

M. Fantini, S. Lisi, P. de los Rios, A. Cattaneo, A. Pastore

This study introduces a method to infer protein structure and evolutionary landscape from functional selection without direct structural determination or physical measurements.

bioRxiv · Feb 4, 2021Evolutionary Biology

Tumors escape immunosurveillance by overexpressing the proteasome activator REGγ

M. Boulpicante, R. Darrigrand, A. Pierson, V. Salgues, B. Gaudineau, M. Khaled, A. Cattaneo, A. Bachi, P. Cascio, S. Apcher

The paper shows cancer cells evade immunosurveillance by upregulating REGγ, which increases destruction of MHC-I peptides generated from nuclear translation products.

bioRxiv · Jan 6, 2019Immunology

The structure of the Pro-domain of mouse proNGF in contact with the NGF domain

R. Yan, H. Yalinca, F. Paoletti, F. Gobbo, L. Marchetti, A. Kuzmanic, D. Lamba, F. L. Gervasio, P. V. Konarev, A. Cattaneo, A. Pastore

This study determines the structure of the pro-domain of mouse proNGF using NMR and SAXS, revealing its intrinsic disorder and functional interactions with mature NGF.

bioRxiv · May 29, 2018Biophysics