De Novo Engineering of Pd-Metalloproteins and Their Use as Intracellular Catalysts

JACS Au Pub Date : 2024-06-23 DOI:10.1021/jacsau.4c00379
Soraya Learte-Aymamí, Laura Martínez-Castro, Carmen González-González, Miriam Condeminas, Pau Martin-Malpartida, María Tomás-Gamasa, Sandra Baúlde, José R. Couceiro, Jean-Didier Maréchal, Maria J. Macias, José L. Mascareñas, M. Eugenio Vázquez
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Abstract

The development of transition metal-based catalytic platforms that promote bioorthogonal reactions inside living cells remains a major challenge in chemical biology. This is particularly true for palladium-based catalysts, which are very powerful in organic synthesis but perform poorly in the cellular environment, mainly due to their rapid deactivation. We now demonstrate that grafting Pd(II) complexes into engineered β-sheets of a model WW domain results in cell-compatible palladominiproteins that effectively catalyze depropargylation reactions inside HeLa cells. The concave shape of the WW domain β-sheet proved particularly suitable for accommodating the metal center and protecting it from rapid deactivation in the cellular environment. A thorough NMR and computational study confirmed the formation of the metal-stapled peptides and allowed us to propose a three-dimensional structure for this novel metalloprotein motif.

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钯金属蛋白新工程及其作为细胞内催化剂的应用
开发能促进活细胞内生物正交反应的过渡金属催化平台仍然是化学生物学领域的一大挑战。钯基催化剂尤其如此,它们在有机合成中非常强大,但在细胞环境中却表现不佳,主要原因是它们会迅速失活。我们现在证明,将 Pd(II) 复合物接枝到模型 WW 结构域的工程化 β 片上,就能产生与细胞兼容的钯多聚蛋白,在 HeLa 细胞内有效催化去丙炔化反应。事实证明,WW结构域β片的凹面形状特别适合容纳金属中心,并保护其在细胞环境中不会迅速失活。通过全面的核磁共振和计算研究,我们证实了金属叠肽的形成,并提出了这种新型金属蛋白图案的三维结构。
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