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
- Citations
- 22
- FWCI
- 2.86
- Field percentile
- top 8%
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
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