Laniado Joshua, Cannon Kevin A, Miller Justin E, Sawaya Michael R, McNamara Dan E, Yeates Todd O
Molecular Biology Institute, UCLA, Los Angeles, California 90095, United States.
Institute for Genomics and Proteomics, UCLA-DOE, Los Angeles, California 90095, United States.
ACS Nano. 2021 Mar 23;15(3):4277-4286. doi: 10.1021/acsnano.0c07167. Epub 2021 Mar 8.
Protein molecules bring a rich functionality to the field of designed nanoscale architectures. High-symmetry protein cages are rapidly finding diverse applications in biomedicine, nanotechnology, and imaging, but methods for their reliable and predictable construction remain challenging. In this study we introduce an approach for designing protein assemblies that combines ideas and favorable elements adapted from recent work. Cubically symmetric cages can be created by combining two simpler symmetries, following recently established principles. Here, two different oligomeric protein components are brought together in a geometrically specific arrangement by their separate genetic fusion to individual components of a heterodimeric coiled-coil polypeptide motif of known structure. Fusions between components are made by continuous α-helices to limit flexibility. After a computational design, we tested 10 different protein cage constructions experimentally, two of which formed larger assemblies. One produced the intended octahedral cage, ∼26 nm in diameter, while the other appeared to produce the intended tetrahedral cage as a minor component, crystallizing instead in an alternate form representing a collapsed structure of lower stoichiometry and symmetry. Geometric distinctions between the two characterized designs help explain the different degrees of success, leading to clearer principles and improved prospects for the routine creation of nanoscale protein architectures using diverse methods.
蛋白质分子为设计纳米级结构领域带来了丰富的功能。高对称性蛋白质笼正在迅速在生物医学、纳米技术和成像领域找到各种应用,但可靠且可预测地构建它们的方法仍然具有挑战性。在本研究中,我们引入了一种设计蛋白质组装体的方法,该方法结合了从近期工作中借鉴的思路和有利元素。根据最近确立的原则,通过结合两种更简单的对称性可以创建立方对称笼。在这里,两种不同的寡聚蛋白质组分通过分别与已知结构的异二聚体卷曲螺旋多肽基序的各个组分进行基因融合,以几何特定排列组合在一起。组分之间的融合由连续的α螺旋构成,以限制灵活性。经过计算设计后,我们通过实验测试了10种不同的蛋白质笼构建体,其中两种形成了更大的组装体。一种产生了预期的八面体笼,直径约为26纳米,而另一种似乎产生了预期的四面体笼作为次要组分,反而以代表较低化学计量和对称性的塌陷结构的另一种形式结晶。两种已表征设计之间的几何差异有助于解释不同程度的成功,从而为使用多种方法常规创建纳米级蛋白质结构带来更清晰的原则和更好的前景。