作者
Robby Divine,Ha V. Dang,George Ueda,Jorge A. Fallas,Ivan Vulovic,William Sheffler,Shally Saini,Yan Ting Zhao,Infencia Xavier Raj,Peter A. Morawski,Madeleine F. Jennewein,Leah J. Homad,Yu-Hsin Wan,Marti R. Tooley,Franziska Seeger,Ali Etemadi,Mitchell L. Fahning,James Lazarovits,Alex Roederer,Alexandra C. Walls,Lance Stewart,Mohammadali Mazloomi,Neil P. King,Daniel Campbell,Andrew T. McGuire,Leonidas Stamatatos,Hannele Ruohola‐Baker,Julie Mathieu,David Veesler,David Baker
摘要
Integrating form and function for design Antibodies are broadly used in therapies and as research tools because they can be generated against a wide range of targets. Efficacy can often be increased by clustering antibodies in multivalent assemblies. Divine et al. designed antibody nanocages from two components: One is an antibody-binding homo-oligomic protein and the other is the antibody itself. Computationally designed proteins drive the assembly of antibody nanocages in a range of architectures, allowing control of the symmetry and the antibody valency. The multivalent display enhances antibody-dependent signaling, and nanocages displaying antibodies against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein effectively neutralize pseudovirus. Science , this issue p. eabd9994