Author

Camila Deride

Austral University of Chile

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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Molecular Biology· 2 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:drug response / drug discovery· 1 Research Focus:host-pathogen & immune response· 1 Assay:proteomics· 1

Frequent Co-Authors

Alejandro Rojas‐FernándeziD· 3 shared Guillermo ValenzuelaiD· 3 shared Johanna Himelreichs· 3 shared Alexander A. KhromykhiD· 2 shared Constanza Salinas-RebolledoiD· 2 shared Daniel WattersoniD· 2 shared Naphak ModhiraniD· 2 shared Pamela EhrenfeldiD· 2 shared

Activity by Year

2021-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersMolecular Biology

Alejandro Rojas‐FernándezORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

A protective bispecific antibody targets both Nipah virus surface glycoproteins and limits viral escape

Ariel Isaacs, Guillermo Valenzuela, Xinghai Zhang, Naphak Modhiran, Jennifer A. Barr, Nazia Thakur, Yu Shang Low, Rhys H. Parry, James B. Barnes, Ronald Jara, Johanna Himelreichs, Yanfeng Yao, Camila Deride, Barbara Barthou-Gatica, Constanza Salinas-Rebolledo, , Daniel Watterson

This paper develops a bispecific antibody that targets both Nipah virus surface glycoproteins, reducing viral escape and enhancing protection against NiV disease.

bioRxiv · Mar 11, 2025 · PreprintMicrobiology

Novel Library Assembly Technique for Developing Nanobodies Targeting IPNv VP2 Protein

Camila Nicole Pino Belmar, Johanna Himelreichs, Camila Deride, Tamara Matúte, Isaac Núñez, Severine Cazaux, Fernán Federici, Karen Moreno, Genaro Soto-Rauch, José Munizaga, Denise Haussmann, Alejandro Rojas-Fernandez, Figueroa V Jaime, Guillermo Valenzuela

This paper develops a novel nanobody library assembly technique for targeting IPNv VP2 protein, identifying specific nanobodies with diagnostic potential.

bioRxiv · Nov 13, 2024 · PreprintMolecular Biology

Potent neutralization of clinical isolates of SARS-CoV-2 D614 and G614 variants by a monomeric, sub-nanomolar affinity Nanobody.

Guillermo Valenzuela, Ronald Jara, Daniel Watterson, Naphak Modhiran, Alberto Anastacio Amarilla, Johanna Himelreichs, Alexander A. Khromykh, Constanza Salinas-Rebolledo, Teresa Pinto, Yorka Cheuquemilla, Yago Margolles, Natalia López‐González del Rey, Zaray Miranda-Chacón, Alexei Cuevas, Anne Berking, , Alejandro Rojas‐Fernández

The paper describes the development of a high-affinity Nanobody against SARS-CoV-2 RBD that neutralizes wild-type and D614G variants with nanomolar potency.

Scientific Reports · Feb 8, 2021Peer-reviewedMolecular Biology