Designed protein logic to target cells with precise combinations of surface antigens
Author(s) -
Marc J. Lajoie,
Scott E. Boyken,
Alexander I. Salter,
Jilliane Bruffey,
Anusha Rajan,
Robert A. Langan,
Audrey Olshefsky,
Vishaka Muhunthan,
Matthew J. Bick,
Mesfin Gewe,
Alfredo QuijanoRubio,
JayLee M. Johnson,
Garreck Lenz,
Alisha Nguyen,
Suzie H. Pun,
Colin Correnti,
Stanley R. Riddell,
David Baker
Publication year - 2020
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aba6527
Subject(s) - antigen , chimeric antigen receptor , microbiology and biotechnology , cell , surface protein , computational biology , biology , computer science , chemistry , t cell , immunology , virology , genetics , immune system
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.
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