Droplet-based screening of phosphate transfer catalysis reveals how epistasis shapes MAP kinase interactions with substrates
| Autor: | Remkes A. Scheele, Laurens H. Lindenburg, Maya Petek, Markus Schober, Kevin N. Dalby, Florian Hollfelder |
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| Přispěvatelé: | Petek, Maya [0000-0002-4597-4162], Dalby, Kevin N [0000-0001-9272-5129], Hollfelder, Florian [0000-0002-1367-6312], Apollo - University of Cambridge Repository |
| Rok vydání: | 2022 |
| Předmět: |
endocrine system
MAP Kinase Signaling System Science 49/47 MAP Kinase Kinase 1 49/23 General Physics and Astronomy 96/35 96/34 631/45/275 General Biochemistry Genetics and Molecular Biology Catalysis Phosphates Substrate Specificity 96/95 Protein Domains Humans Phosphorylation Mitogen-Activated Protein Kinase 1 49/31 Multidisciplinary 631/45/603 article Epistasis Genetic General Chemistry 631/92/605 Protein-Tyrosine Kinases Molecular Docking Simulation 631/92/552 631/1647/2163 Mitogen-Activated Protein Kinases Protein Kinases Signal Transduction |
| Zdroj: | Nature Communications, Vol 13, Iss 1, Pp 1-14 (2022) |
| DOI: | 10.17863/cam.80115 |
| Popis: | The combination of ultrahigh-throughput screening and sequencing informs on function and intragenic epistasis within combinatorial protein mutant libraries. Establishing a droplet-based, in vitro compartmentalised approach for robust expression and screening of protein kinase cascades (>107 variants/day) allowed us to dissect the intrinsic molecular features of the MKK-ERK signalling pathway, without interference from endogenous cellular components. In a six-residue combinatorial library of the MKK1 docking domain, we identified 29,563 sequence permutations that allow MKK1 to efficiently phosphorylate and activate its downstream target kinase ERK2. A flexibly placed hydrophobic sequence motif emerges which is defined by higher order epistatic interactions between six residues, suggesting synergy that enables high connectivity in the sequence landscape. Through positive epistasis, MKK1 maintains function during mutagenesis, establishing the importance of co-dependent residues in mammalian protein kinase-substrate interactions, and creating a scenario for the evolution of diverse human signalling networks. RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) - BB/M011194/1 EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) - 721613 EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) - 659029 EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) - 695669 |
| Databáze: | OpenAIRE |
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