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<p>Many proteins function as switches, transducing the concentrations of environmental chemicals into cellular responses. It is not well understood how signal processing by switches is genetically encoded. Here, using a massively parallel approach, GluePCA, we present &gt;40,000 measurements and a complete map of how mutations alter the quantitative&#xa0;activation function of a receptor switch, the plant hormone sensor PYL1. Close to 90% of missense variants tune the dose-response of the receptor, often causing correlated changes in sensitivity, basal activity, maximum response and induction steepness. Based on theory we predict and then validate the underlying latent mechanism as a change in protein stability. Beyond this, signalling parameters can be independently tuned, with large effects in interface-distal positions and a modular genetic architecture across the receptor’s structure. Rare single amino acid substitutions confer phenotypic innovation, including inverted and band-stop activation functions. Our data demonstrate the feasibility of dose-response profile quantification at massive scale and reveal the remarkable evolutionary malleability of a protein switch.</p>

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The genetic architecture of an allosteric hormone receptor

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年4月1日

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  • Maximilian R. Stammnitz,
  • Ben Lehner

摘要

Many proteins function as switches, transducing the concentrations of environmental chemicals into cellular responses. It is not well understood how signal processing by switches is genetically encoded. Here, using a massively parallel approach, GluePCA, we present >40,000 measurements and a complete map of how mutations alter the quantitative activation function of a receptor switch, the plant hormone sensor PYL1. Close to 90% of missense variants tune the dose-response of the receptor, often causing correlated changes in sensitivity, basal activity, maximum response and induction steepness. Based on theory we predict and then validate the underlying latent mechanism as a change in protein stability. Beyond this, signalling parameters can be independently tuned, with large effects in interface-distal positions and a modular genetic architecture across the receptor’s structure. Rare single amino acid substitutions confer phenotypic innovation, including inverted and band-stop activation functions. Our data demonstrate the feasibility of dose-response profile quantification at massive scale and reveal the remarkable evolutionary malleability of a protein switch.