Rational engineering of DNA-nanoparticle motor with high speed and processivity comparable to motor proteins

IF 15.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Nature Communications Pub Date : 2025-01-16 DOI:10.1038/s41467-025-56036-0
Takanori Harashima, Akihiro Otomo, Ryota Iino
{"title":"Rational engineering of DNA-nanoparticle motor with high speed and processivity comparable to motor proteins","authors":"Takanori Harashima, Akihiro Otomo, Ryota Iino","doi":"10.1038/s41467-025-56036-0","DOIUrl":null,"url":null,"abstract":"<p>DNA-nanoparticle motor is a burnt-bridge Brownian ratchet moving on RNA-modified surface driven by Ribonuclease H (RNase H), and one of the fastest nanoscale artificial motors. However, its speed is still much lower than those of motor proteins. Here we resolve elementary processes of motion and reveal long pauses caused by slow RNase H binding are the bottleneck. As RNase H concentration ([RNase H]) increases, pause lengths shorten from ~70 s to ~0.2 s, while step sizes (displacements between two consecutive pauses) are constant ( ~ 20 nm). At high [RNase H], speed reaches ~100 nm s<sup>−1</sup>, however, processivity (total number of steps before detachment), run-length, and unidirectionality largely decrease. A geometry-based kinetic simulation reveals switching of bottleneck from RNase H binding to DNA/RNA hybridization at high [RNase H], and trade-off mechanism between speed and other performances. An engineered motor with 3.8-times larger DNA/RNA hybridization rate simultaneously achieves 30 nm s<sup>−1</sup> speed, 200 processivity, and 3 μm run-length comparable to motor proteins.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"31 1","pages":""},"PeriodicalIF":15.7000,"publicationDate":"2025-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-025-56036-0","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

DNA-nanoparticle motor is a burnt-bridge Brownian ratchet moving on RNA-modified surface driven by Ribonuclease H (RNase H), and one of the fastest nanoscale artificial motors. However, its speed is still much lower than those of motor proteins. Here we resolve elementary processes of motion and reveal long pauses caused by slow RNase H binding are the bottleneck. As RNase H concentration ([RNase H]) increases, pause lengths shorten from ~70 s to ~0.2 s, while step sizes (displacements between two consecutive pauses) are constant ( ~ 20 nm). At high [RNase H], speed reaches ~100 nm s−1, however, processivity (total number of steps before detachment), run-length, and unidirectionality largely decrease. A geometry-based kinetic simulation reveals switching of bottleneck from RNase H binding to DNA/RNA hybridization at high [RNase H], and trade-off mechanism between speed and other performances. An engineered motor with 3.8-times larger DNA/RNA hybridization rate simultaneously achieves 30 nm s−1 speed, 200 processivity, and 3 μm run-length comparable to motor proteins.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
具有可与马达蛋白媲美的高速度和加工能力的dna纳米粒子马达的合理工程设计
dna纳米马达是一种以核糖核酸酶H (RNase H)为驱动,在rna修饰表面上运动的烧桥布朗棘轮,是目前最快的纳米级人工马达之一。但其速度仍远低于运动蛋白。在这里,我们解决了基本的运动过程,并揭示了由缓慢的RNase H结合引起的长时间停顿是瓶颈。随着RNase H浓度([RNase H])的增加,暂停长度从~70 s缩短到~0.2 s,而步长(两个连续暂停之间的位移)是恒定的(~ 20 nm)。在高[RNase H]时,速度达到~100 nm s - 1,但加工效率(分离前的总步数)、行程长度和单向性大大降低。基于几何的动力学模拟揭示了瓶颈从RNase H结合到高[RNase H]下DNA/RNA杂交的转换,以及速度和其他性能之间的权衡机制。具有3.8倍DNA/RNA杂交率的工程马达同时实现30 nm s - 1速度,200的处理速率和3 μm的运行长度与马达蛋白相当。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Nature Communications
Nature Communications Biological Science Disciplines-
CiteScore
24.90
自引率
2.40%
发文量
6928
审稿时长
3.7 months
期刊介绍: Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.
期刊最新文献
Catalytic Proximal Protein Oligomerization as an Anti-Tumor Strategy Targeting WDR5. Recycling senescent cell lipids for targeted senotherapy. Structure of a pH-sensitive pentameric ligand-gated ion channel from the Sarcoptes scabies mite. The COP1-ADA2b module mediates light regulation of DNA double-strand break repair in Arabidopsis. The evolutionary consequences of behavioural plasticity.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1