Construction of a novel phagemid to produce custom DNA origami scaffolds

IF 3.2 4区 生物学 Q1 Agricultural and Biological Sciences Synthetic Biology Pub Date : 2018-04-27 DOI:10.1101/309682
Parsa M. Nafisi, Tural Aksel, Shawn M. Douglas
{"title":"Construction of a novel phagemid to produce custom DNA origami scaffolds","authors":"Parsa M. Nafisi, Tural Aksel, Shawn M. Douglas","doi":"10.1101/309682","DOIUrl":null,"url":null,"abstract":"DNA origami, a method for constructing nanoscale objects, relies on a long single strand of DNA to act as the “scaffold” to template assembly of numerous short DNA oligonucleotide “staples”. The ability to generate custom scaffold sequences can greatly benefit DNA origami design processes. Custom scaffold sequences can provide better control of the overall size of the final object and better control of low-level structural details, such as locations of specific base pairs within an object. Filamentous bacteriophages and related phagemids can work well as sources of custom scaffold DNA. However, scaffolds derived from phages require inclusion of multi-kilobase DNA sequences in order to grow in host bacteria, and thus cannot be altered or removed. These fixed-sequence regions constrain the design possibilities of DNA origami. Here we report the construction of a novel phagemid, pScaf, to produce scaffolds that have a custom sequence with a much smaller fixed region of only 381 bases. We used pScaf to generate new scaffolds ranging in size from 1,512 to 10,080 bases and demonstrated their use in various DNA origami shapes and assemblies. We anticipate our pScaf phagemid will enhance development of the DNA origami method and its future applications.","PeriodicalId":22158,"journal":{"name":"Synthetic Biology","volume":"8 1","pages":""},"PeriodicalIF":3.2000,"publicationDate":"2018-04-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"36","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Synthetic Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1101/309682","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Agricultural and Biological Sciences","Score":null,"Total":0}
引用次数: 36

Abstract

DNA origami, a method for constructing nanoscale objects, relies on a long single strand of DNA to act as the “scaffold” to template assembly of numerous short DNA oligonucleotide “staples”. The ability to generate custom scaffold sequences can greatly benefit DNA origami design processes. Custom scaffold sequences can provide better control of the overall size of the final object and better control of low-level structural details, such as locations of specific base pairs within an object. Filamentous bacteriophages and related phagemids can work well as sources of custom scaffold DNA. However, scaffolds derived from phages require inclusion of multi-kilobase DNA sequences in order to grow in host bacteria, and thus cannot be altered or removed. These fixed-sequence regions constrain the design possibilities of DNA origami. Here we report the construction of a novel phagemid, pScaf, to produce scaffolds that have a custom sequence with a much smaller fixed region of only 381 bases. We used pScaf to generate new scaffolds ranging in size from 1,512 to 10,080 bases and demonstrated their use in various DNA origami shapes and assemblies. We anticipate our pScaf phagemid will enhance development of the DNA origami method and its future applications.
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
构建一种新型噬菌体以生产定制DNA折纸支架
DNA折纸是一种构建纳米级物体的方法,它依靠一条长单链DNA作为“支架”,将许多短DNA寡核苷酸“订书钉”组装成模板。产生定制支架序列的能力可以极大地有利于DNA折纸设计过程。定制支架序列可以更好地控制最终对象的整体尺寸,更好地控制底层结构细节,例如对象内特定碱基对的位置。丝状噬菌体和相关的噬菌体可以很好地作为定制支架DNA的来源。然而,来自噬菌体的支架需要包含多千碱基DNA序列才能在宿主细菌中生长,因此不能被改变或移除。这些固定序列区域限制了DNA折纸设计的可能性。在这里,我们报道了一种新的噬菌体pScaf的构建,以产生具有定制序列的支架,其固定区域更小,只有381个碱基。我们使用pScaf生成新的支架,其大小从1,512到10,080个碱基不等,并演示了它们在各种DNA折纸形状和组装中的使用。我们期望我们的pScaf噬菌体将促进DNA折纸方法的发展及其未来的应用。
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
Synthetic Biology
Synthetic Biology Agricultural and Biological Sciences-Agricultural and Biological Sciences (miscellaneous)
CiteScore
4.50
自引率
3.10%
发文量
28
审稿时长
25 weeks
期刊最新文献
Utilizing a Cell-free Protein Synthesis Platform for the Biosynthesis of a Natural Product, Caffeine Advancing reproducibility can ease the ‘hard truths’ of synthetic biology Efficient and iterative retron-mediated in vivo recombineering in Escherichia coli Xer recombination for the automatic deletion of selectable marker genes from plasmids in enteric bacteria Development of synthetic biotics as treatment for human diseases
×
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:481959085
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