Designed architectural proteins that tune DNA looping in bacteria.
David H TseNicole A BeckerRobert T YoungWilma K OlsonJustin P PetersTanya L SchwabKarl J ClarkLouis James Maher IiiPublished in: Nucleic acids research (2021)
Architectural proteins alter the shape of DNA. Some distort the double helix by introducing sharp kinks. This can serve to relieve strain in tightly-bent DNA structures. Here, we design and test artificial architectural proteins based on a sequence-specific Transcription Activator-like Effector (TALE) protein, either alone or fused to a eukaryotic high mobility group B (HMGB) DNA-bending domain. We hypothesized that TALE protein binding would stiffen DNA to bending and twisting, acting as an architectural protein that antagonizes the formation of small DNA loops. In contrast, fusion to an HMGB domain was hypothesized to generate a targeted DNA-bending architectural protein that facilitates DNA looping. We provide evidence from Escherichia coli Lac repressor gene regulatory loops supporting these hypotheses in living bacteria. Both data fitting to a thermodynamic DNA looping model and sophisticated molecular modeling support the interpretation of these results. We find that TALE protein binding inhibits looping by stiffening DNA to bending and twisting, while the Nhp6A domain enhances looping by bending DNA without introducing twisting flexibility. Our work illustrates artificial approaches to sculpt DNA geometry with functional consequences. Similar approaches may be applicable to tune the stability of small DNA loops in eukaryotes.
Keyphrases
- circulating tumor
- cell free
- single molecule
- escherichia coli
- nucleic acid
- magnetic resonance
- amino acid
- computed tomography
- magnetic resonance imaging
- machine learning
- small molecule
- protein protein
- transcription factor
- drug delivery
- dendritic cells
- mass spectrometry
- multidrug resistant
- candida albicans
- cancer therapy
- toll like receptor
- nuclear factor
- big data
- dna binding
- klebsiella pneumoniae