折叠(DSP实现)
力谱学
蛋白质折叠
计算生物学
DNA折纸
DNA
生物物理学
钙结合蛋白
化学
能源景观
钙
纳米技术
生物
原子力显微镜
生物化学
材料科学
工程类
有机化学
电气工程
作者
Honglu Zhang,Cristhian Cañari-Chumpitaz,Lisa Alexander,Huan Zhang,Chunhai Fan,Carlos Bustamante
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2025-05-01
卷期号:11 (18)
标识
DOI:10.1126/sciadv.adv1962
摘要
Understanding the intricate folding process of proteins and characterizing the intermediates they populate en route to their native state remain challenging despite the remarkable accuracy achieved through in silico approaches for predicting native protein structures. Here, we replaced the conventional flexible double-stranded DNA handle force transducers with solid DNA-origami bundles to conduct single-molecule folding force-spectroscopy studies on calerythrin, a compact multidomain calcium-binding globular protein. The resulting origami-enhanced data revealed a previously "hidden" folding intermediate and the hierarchical nature of the protein's folding pathway. A systematic comparison of the AlphaFold-predicted conformational ensemble of structures of the native state and folding intermediates across various calcium-binding proteins provides a structural rationalization for the folding behavior of this protein family. The integration of DNA origami-enhanced single-molecule experiments with in silico approaches, and structural analysis presented here, constitutes a comprehensive method to uncover the rules underlying the formation of intermediates within protein folding landscapes.
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