QTY code-designed water-soluble Fc-fusion cytokine receptors bind to their respective ligands

Cytokine release syndrome (CRS), or "cytokine storm", is the leading side effect during CAR-T therapy that is potentially life-threatening It also plays a critical role in viral infections such as COVID-19 Therefore, efficient removal of excessive cytokines is essential for treatment We previously reported a novel protein modification tool called the QTY code, through which hydrophobic amino acids Leu, Ile, Val and Phe are replaced by Gln (Q), Thr (T) and Tyr (Y) Thus the functional detergent-free equivalent of membrane proteins can be designed Here we report the application of the QTY code on six variants of cytokine receptors, including interleukin receptors IL4αR and IL10αR, chemokine receptors CCR9 and CXCR2, as well as interferon receptors IFNγR1 and IFNλR1 QTY-variant cytokine receptors exhibit physiol properties similar to those of native receptors without the presence of hydrophobic segments The receptors were fused to the Fc region of IgG protein to form an antibody-like structure These QTY code-designed Fc fusion receptors were expressed in E coli and purified The resulting water-soluble fusion receptors bind to their resp ligands with Kd values affinity similar to isolated native receptors Our cytokine receptor-Fc fusion proteins potentially serve as an antibody-like decoy to dampen the excessive cytokine levels associated with CRS and COVID-19 infection