| Literature DB >> 32820060 |
Marc J Lajoie1,2, Scott E Boyken3,2, Alexander I Salter4,5, Jilliane Bruffey3,2,6, Anusha Rajan4,5, Robert A Langan3,2, Audrey Olshefsky3,7, Vishaka Muhunthan4,5, Matthew J Bick3,2, Mesfin Gewe5, Alfredo Quijano-Rubio3,2,7, JayLee Johnson3, Garreck Lenz3, Alisha Nguyen3, Suzie Pun7,8, Colin E Correnti5, Stanley R Riddell4,5,9, David Baker1,2,10.
Abstract
Precise cell targeting is challenging because most mammalian cell types lack a single surface marker that distinguishes them from other cells. A solution would be to target cells using specific combinations of proteins present on their surfaces. In this study, we design colocalization-dependent protein switches (Co-LOCKR) that perform AND, OR, and NOT Boolean logic operations. These switches activate through a conformational change only when all conditions are met, generating rapid, transcription-independent responses at single-cell resolution within complex cell populations. We implement AND gates to redirect T cell specificity against tumor cells expressing two surface antigens while avoiding off-target recognition of single-antigen cells, and three-input switches that add NOT or OR logic to avoid or include cells expressing a third antigen. Thus, de novo designed proteins can perform computations on the surface of cells, integrating multiple distinct binding interactions into a single output.Entities:
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Year: 2020 PMID: 32820060 PMCID: PMC8085813 DOI: 10.1126/science.aba6527
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728