Author
S. Hernandez-Perez
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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2019-2023 · peak 2/yrCo-Author Collaboration Network
10 top collaborators · 36 mutual co-author links6 papers
Recent·Most cited
Proteomic profiling of isolated immune synapses from primary mouse B cells
D. M. Cunha, S. Hernandez-Perez, L. O. Awoniyi, A. F. Carisey, G. Jacquemet, P. Mattila
This study isolates and profiles immune synapses from primary mouse B cells to identify proteins involved in early activation by surface-bound antigens, revealing novel components and pathways.
bioRxiv · Feb 23, 2023 · PreprintImmunology
Loss of Rab8a in B cells leads to increased antibody responses and class-switch recombination
S. Hernandez-Perez, A. V. Sarapulov, M. O. Balci, E. Coffey, A. Harada, P. Mattila
This study shows that Rab8a deficiency in B cells increases antibody responses and class-switch recombination by altering signaling pathways.
bioRxiv · Sep 19, 2022 · PreprintImmunology
BCR-induced protein dynamics and the emerging role of SUMOylation revealed by proximity proteomics
L. O. Awoniyi, A. V. Sarapulov, S. Hernandez-Perez, M. Runsala, D. M. Cunha, B. Tejeda-Gonzalez, V. Sustar, M. O. Balci, P. Petrov, P. K. Mattila
This study uses proximity proteomics to identify dynamic protein changes and SUMOylation events in BCR activation, revealing new roles in signaling pathways.
bioRxiv · Sep 29, 2020 · PreprintImmunology
Missing-In-Metastasis / Metastasis Suppressor 1 modulates B cell receptor signaling, B cell metabolic potential and T cell-independent immune responses.
A. V. Sarapulov, P. Petrov, S. Hernandez-Perez, V. Sustar, E. Kuokkanen, R. Vinod, M. Vainio, L. Cords, M. Fritzsche, Y. Carrasco, P. Mattila
This study shows that MIM/MTSS1 regulates B cell receptor signaling, metabolic activity, and T cell-independent immune responses, with implications for cancer biology.
bioRxiv · Mar 8, 2020Immunology
B cells rapidly target antigen and surface-derived MHCII into peripheral degradative compartments.
S. Hernandez-Perez, M. Vainio, E. Kuokkanen, V. Sustar, P. Petrov, S. Forsten, V. Paavola, J. Rajala, L. Awoniyi, A. Sarapulov, H. Vihinen, E. Jokitalo, A. Bruckbauer, P. Mattila
This study identifies specialized early peripheral acidic vesicles (eMIIC) in B cells that facilitate rapid antigen processing and MHCII peptide loading for immune response.
bioRxiv · Oct 30, 2019Immunology