@misc{brodel_rodrigues_jaramillo_isalan_2019, 
  title={Engineering the smallest transcription factor: accelerated evolution of a 63-amino acid peptide dual activator-repressor}, 
  DOI={10.1101/725739}, 
  abstractNote={<jats:p>Transcription factors control gene expression in all life. This raises the question of what is the smallest protein that can support such activity. In nature, Cro from bacteriophage λ is the smallest known repressor (66 amino acids; a.a.) but activators are typically much larger (e.g. λ cI, 237 a.a.). Indeed, previous efforts to engineer a minimal activator from Cro resulted in no activity in vivo. In this study, we show that directed evolution results in a new Cro activator-repressor that functions as efficiently as λ cI, in vivo. To achieve this, we develop Phagemid-Assisted Continuous Evolution: PACEmid. We find that a peptide as small as 63-a.a. functions efficiently as an activator and/or repressor. To our knowledge, this is the smallest protein gene regulator reported to date, highlighting the capacity of transcription factors to evolve from very short peptide sequences.</jats:p>}, 
  publisher={Cold Spring Harbor Laboratory}, 
  author={Brodel, Andreas Klaus and Rodrigues, Rui and Jaramillo, Alfonso and Isalan, Mark}, 
  year={2019}, 
  month={Aug}
  }