Skeletides: A Modular, Simplified Physical Model of Protein Secondary Structure

被引:0
|
作者
Asachi, Parsa [1 ]
Nguyen, Uyen N. T. [1 ]
Dang, Jacqueline [1 ]
Spencer, Ryan K. [2 ]
Martin, Hannah S. [1 ]
Zuckermann, Ronald N. [1 ]
机构
[1] Lawrence Berkeley Natl Lab, Mol Foundry, 1 Cyclotron Rd, Berkeley, CA 94720 USA
[2] Univ Calif Irvine, Dept Chem Engn, Irvine, CA USA
关键词
molecular models; 3D printing; self-assembly; protein structure; amino acids; conformational analysis; BACKBONE RECONSTRUCTION; VALIDATION;
D O I
10.1089/3dp.2019.0121
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Three-dimensional (3D) models are essential for visualization and conceptual understanding of complex architectures such as protein structure. Although there is a plethora of software platforms that allow digital depictions of protein structure at an atomic level in silico, physical models are needed to convey an intuitive understanding of biomolecular architecture. However, it is a challenge to represent all the relevant features of proteins in a single physical model due to their sheer structural complexity. Here, we describe a modular protein model that focuses only on representation of the secondary structure-the underlying structural skeleton. The simplified model consists of amino acid units, which can be linked together to reproduce the two most fundamental structural features of protein secondary structure: the relative positions of the amino acid alpha carbon atoms, and the intra-main chain hydrogen bonding pattern. We use 3D printing and magnets to create a set of three modular amino acid building blocks, which when linked together into a chain, can faithfully represent alpha helices, beta sheets, and turns. These simple to make models can be used to quickly assemble the alpha carbon trace of an entire protein domain, which conveys a tactile experience of the complexity of protein skeletal architecture. These models highlight the modularity of protein structure: where a single structural unit, the amino acid, can be linked together to form a larger, regular secondary structure. These models also have a propensity to spontaneously organize into alpha helices and beta sheets, as demonstrated by their ability to autonomously assemble when placed in a circulating water tank. These models provide a missing educational tool to expand knowledge of protein structure, foster deeper insight into protein folding, and inspire greater interest in biomacromolecular architecture.
引用
收藏
页码:60 / 69
页数:10
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