Cell DiscoverySynthetic BiologyPeer-reviewed journal article
Designed allosteric protein logic
Tjaša PlaperiD, Estera MerljakiD, Tina FinkiD, Tadej SatleriD, Ajasja LjubetičiD, Duško LainščekiD, Vid JazbeciD, Mojca BenčinaiD, Sintija Stevanoska, Sašo DžeroskiiD, Roman JeralaiD
Abstract
Regulation of the activity of proteins enables control of complex cellular processes. Allosteric regulation has been introduced individually into few natural proteins. Here, we present a generally applicable regulation of diverse proteins called INSRTR (inserted peptide structure regulator), based on inserting a short unstructured peptide into a solvent-accessible loop that retains protein function. Function of the target protein can be inactivated by the addition of a peptide that forms a rigid coiled-coil dimer. This platform enables the construction of ON/OFF protein switches, their regulation by small molecules, and Boolean logic functions with a rapid response in mammalian cells. INSRTR can be used to regulate a wide range of proteins, as demonstrated on ten members of protein families with diverse biological activities including enzymes, signaling mediators, DNA binders/transcriptional regulators, fluorescent protein, and antibodies regulating chimeric antigen receptor. INSRTR platform presents an extraordinary potential for regulating biological systems and applications. One sentence summaryAuthors have designed a widely applicable system to activate or inactivate function of diverse proteins or form Boolean logic gates based on formation of a coiled-coil dimer within protein loops and demonstrated its implementation on a range of 10 diverse proteins.
- assay: protein structure
- research focus: protein design
- research focus: drug response / drug discovery
- research focus: perturbation response prediction
- approach: experimental assay
- Citations
- 22
- FWCI
- 2.86
- Field percentile
- top 8%
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