Learte-Aymamí Soraya, Martínez-Castro Laura, González-González Carmen, Condeminas Miriam, Martin-Malpartida Pau, Tomás-Gamasa María, Baúlde Sandra, Couceiro José R, Maréchal Jean-Didier, Macias Maria J, Mascareñas José L, Vázquez M Eugenio
Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares (CiQUS), Departamento de Química Orgánica, Universidade de Santiago de Compostela, Santiago de Compostela 15705, Spain.
Insilichem, Departament de Química, Universitat Autónoma de Barcelona, Cerdanyola 08193, Spain.
JACS Au. 2024 Jun 23;4(7):2630-2639. doi: 10.1021/jacsau.4c00379. eCollection 2024 Jul 22.
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.
开发能够促进活细胞内生物正交反应的过渡金属基催化平台仍然是化学生物学中的一项重大挑战。对于钯基催化剂而言尤其如此,这类催化剂在有机合成中非常有效,但在细胞环境中表现不佳,主要是因为它们会迅速失活。我们现在证明,将钯(II)配合物接枝到模型WW结构域的工程化β折叠中会产生细胞相容的钯微型蛋白,其能够在HeLa细胞内有效催化脱炔丙基反应。事实证明,WW结构域β折叠的凹形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。全面的核磁共振和计算研究证实了金属固定肽的形成,并使我们能够为这种新型金属蛋白基序提出三维结构。