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Jordan R. Barrett on Muck Rack

Jordan R. Barrett

As seen in: Nature, Wiley Online Library, BioRxiv, Cell Press, Cell Reports Medicine, DEV Community
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Articles

Analysis of monoclonal antibodies against the malaria invasion complex protein RIPR reveals the structural basis for synergistic antibody protection

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By Barnabas G Williams, Jordan R. Barrett, Josefin Bartholdson Scott, Cassandra A Rigby, Matteo Cagiada, Doris Quinkert, Kirsty McHugh, Anna Huhn, Sean A. Burnap, Camille Gourjault, Francesca Byrne, Ana Rodrigues, Laura Bergamaschi, Simon Watson, Noah W. Miller, Lloyd D.W. King, Francesca R Donnellan, Camilla A. Gladstone, Sarah Silk, Jo Salkeld, Angela M Minassian, Katherine Skinner, Weston Struwe, Charlotte M. Deane, Stephen T. Reece, Andrew Ward, Simon Draper, Beatrice Balzarotti, Jemima Paterson, Stefania Scalabrino
| Cell Press Verified
Keywords malaria monoclonal antibodies RIPR vaccines Plasmodium falciparum mAb blood stage Introduction Malaria disease, caused by the parasite Plasmodium falciparum, is a global health problem with an estimated 282 million cases in 2024.1 The WHO currently recommends two malaria vaccines, RTS/S/AS01 and R21/Matrix-M2; however, both vaccines target the same pre-erythrocytic sporozoite stage of the parasite life cycle.
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What I learned from my first week in Rust

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By Jordan R. Barrett, Jacob A. Barrett
| DEV Community
Rust is a modern programming language with unique memory safety features that make it particularly suitable for systems programming. Its first stable release (1.0) was in 2015, and since then it's been gradually gaining popularity, especially for low-level programming and performance-critical applications. I've been wanting to learn Rust for a while, and this week I finally took the leap.
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Preclinical development of a stabilized RH5 virus-like particle vaccine that induces improved antimalarial antibodies

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By David Pulido, Jordan R. Barrett, Lloyd D.W. King, Hannah Davies
| Cell Reports Medicine Verified
Highlights • Inhibitory antibodies from RH5.1/AS01B vaccinees target the RH5 α-helical core • A truncated and thermostabilized RH5.2 immunogen induces more potent antibodies • Bioconjugation of RH5.2 to VLPs enhances antibody immunogenicity in rodents • RH5.2-VLP/Matrix-M induces highest functional antimalarial antibodies in rats Summary Plasmodium falciparum reticulocyte-binding protein homolog 5 (RH5) is a leading blood-stage malaria vaccine antigen target, currently in a phase 2b clinical...
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