Perez-Chirinos Laura, Almonte Lisa, Cortés-Ossa Juan David, Solano Eduardo, Calvo M Reyes, Sasselli Ivan R, Cortajarena Aitziber L
Center for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), Paseo de Miramón 194, Donostia-San Sebastián 20014, Spain.
Instituto Universitario de Materiales de Alicante (IUMA), Universidad de Alicante, Alicante 03690, Spain.
ACS Nano. 2025 May 6;19(17):16500-16516. doi: 10.1021/acsnano.4c18613. Epub 2025 Apr 25.
The natural self-assembly tendency of proteins to build complex structural architectures has kindled inspiration in developing supramolecular structures through the rational design of biomacromolecules. While there has been significant progress in achieving precise control over the morphology of self-assembled structures, combining different molecules within assemblies enables the design of materials with increased complexity, sophisticated structures, and a broad spectrum of functionalities. Here, the development of 1D and 2D peptide-protein coassembled systems based on the design of amphiphilic peptides and engineered proteins is described. The peptide was optimized to form stable self-assembled fibers by evaluating, computationally and experimentally, the assembling tendencies and the supramolecular features of peptides with different lengths and negative charges. A superhelical repeat protein was engineered by fusing one or two amphiphilic peptides into one or both termini. This modification drove the coassembly between the self-assembled fibers and the protein with one or two peptides, resulting in 1D or 2D coassembled systems. The protein films and the 2D coassembled system exhibited high ionic conductivity for a biomolecular system, attributed to their high content of charged residues, positioning these materials as promising candidates for developing bioelectronic devices. Thus, this work provides a versatile framework for developing coassembled materials with tunable dimensionality by using biocompatible building blocks without any additional chemical moieties, highlighting the potential for their use in biocompatible electronics.
蛋白质构建复杂结构架构的自然自组装倾向,激发了人们通过合理设计生物大分子来开发超分子结构的灵感。虽然在实现对自组装结构形态的精确控制方面已经取得了重大进展,但在组装体中结合不同分子能够设计出具有更高复杂性、更精细结构和广泛功能的材料。在此,描述了基于两亲性肽和工程化蛋白质设计的一维和二维肽 - 蛋白质共组装系统的开发。通过计算和实验评估不同长度和负电荷的肽的组装倾向和超分子特征,对肽进行了优化以形成稳定的自组装纤维。通过将一个或两个两亲性肽融合到一个或两个末端来设计超螺旋重复蛋白。这种修饰促使自组装纤维与带有一个或两个肽的蛋白质之间发生共组装,从而形成一维或二维共组装系统。蛋白质膜和二维共组装系统在生物分子系统中表现出高离子电导率,这归因于它们高含量的带电残基,使这些材料成为开发生物电子器件的有前途的候选材料。因此,这项工作提供了一个通用框架,用于通过使用生物相容性构建块开发具有可调维度的共组装材料,而无需任何额外的化学基团,突出了它们在生物相容性电子学中的应用潜力。