VEGAS as a Platform for Facile Directed Evolution in Mammalian Cells
Author(s) -
Justin G. English,
Reid H. J. Olsen,
Katherine Lansu,
Michael Patel,
Karoline White,
Adam S. Cockrell,
Darshan Singh,
Ryan T. Strachan,
Daniel Wacker,
Bryan L. Roth
Publication year - 2019
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2019.05.051
Subject(s) - biology , las vegas , computational biology , evolutionary biology , microbiology and biotechnology , medicine , metropolitan area , pathology
Directed evolution, artificial selection toward designed objectives, is routinely used to develop new molecular tools and therapeutics. Successful directed molecular evolution campaigns repeatedly test diverse sequences with a designed selective pressure. Unicellular organisms and their viral pathogens are exceptional for this purpose and have been used for decades. However, many desirable targets of directed evolution perform poorly or unnaturally in unicellular backgrounds. Here, we present a system for facile directed evolution in mammalian cells. Using the RNA alphavirus Sindbis as a vector for heredity and diversity, we achieved 24-h selection cycles surpassing 10 -3 mutations per base. Selection is achieved through genetically actuated sequences internal to the host cell, thus the system's name: viral evolution of genetically actuating sequences, or "VEGAS." Using VEGAS, we evolve transcription factors, GPCRs, and allosteric nanobodies toward functional signaling endpoints each in less than 1 weeks' time.
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