Chemistry Department, New York University, 100 Washington Square E, New York, NY 10003, USA.
X-ray Science Division, Argonne National Laboratory, Lemont, IL 60439, USA.
Angew Chem Int Ed Engl. 2022 Jul 4;61(27):e202201895. doi: 10.1002/anie.202201895. Epub 2022 May 5.
Despite recent progress, it remains challenging to program biomacromolecules to assemble into discrete nanostructures with pre-determined sizes and topologies. We report here a novel strategy to address this challenge. By using two orthogonal pairs of heterodimeric coiled coils as the building blocks, we constructed six discrete supramolecular assemblies, each composed of a prescribed number of coiled coil components. Within these assemblies, different coiled coils were connected via end-to-side covalent linkages strategically pre-installed between the non-complementary pairs. The overall topological features of two highly complex assemblies, a "barbell" and a "quadrilateral" form, were characterized experimentally and were in good agreement to the designs. This work expands the design paradigms for peptide-based discrete supramolecular assemblies and will provide a route for de novo fabrication of functional protein materials.
尽管最近取得了一些进展,但仍然难以将生物大分子编程成具有预定尺寸和拓扑结构的离散纳米结构。我们在这里报告了一种解决这一挑战的新策略。通过使用两对正交的异二聚体卷曲螺旋作为构建块,我们构建了六个离散的超分子组装体,每个组装体由预定数量的卷曲螺旋组成。在这些组装体中,不同的卷曲螺旋通过在非互补对之间预先安装的末端到侧的共价键连接。两种高度复杂的组装体,一个“哑铃”和一个“四边形”形式的整体拓扑特征,通过实验进行了表征,并与设计相符。这项工作扩展了基于肽的离散超分子组装体的设计范例,并将为功能蛋白材料的从头制造提供一条途径。