Author

I. de la Arada

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

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Approach:experimental assay· 1 Research Focus:host-pathogen & immune response· 1 Approach:mechanistic / dynamical model· 1 Research Focus:protein folding & dynamics· 1 Assay:protein structure· 1 Approach:statistical model· 1

Frequent Co-Authors

C. M. Dobson· 1 shared F. Goni· 1 shared H. OSTOLAZA· 1 shared J. AMUATEGI· 1 shared J. D. Camino· 1 shared J. L. R. Arrondo· 1 shared J. Sot· 1 shared N. Cremades· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperBiophysics

C. M. Dobson

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2 papers

Recent·Most cited

Membrane-penetrating peptide from the translocation region of Bordetella Adenylate Cyclase Toxin prevents toxin cytotoxicity on target cells

J. AMUATEGI, R. ALONSO, I. DE LA ARADA, H. OSTOLAZA

The paper identifies a peptide from Bordetella Adenylate Cyclase Toxin that blocks its cytotoxicity by competing for membrane binding.

bioRxiv · Apr 18, 2023 · PreprintBiophysics

The extent of protein hydration dictates the preference for heterogeneous or homogeneous nucleation generating either parallel or antiparallel β-sheet α-synuclein aggregates

J. D. Camino, P. Gracia, S. W. Chen, J. Sot, I. de la Arada, V. Sebastian, J. L. R. Arrondo, F. Goni, C. M. Dobson, N. Cremades

This study shows that α-synuclein can form amyloid aggregates via homogeneous nucleation under limited hydration, leading to antiparallel β-sheet structures, which are more stable than parallel ones under such conditions.

bioRxiv · Sep 28, 2020Biophysics