K Cervantes-Salguero, M Freeley, R E A Gwyther, D D Jones, J L Chávez, M Palma
{"title":"Single molecule DNA origami nanoarrays with controlled protein orientation.","authors":"K Cervantes-Salguero, M Freeley, R E A Gwyther, D D Jones, J L Chávez, M Palma","doi":"10.1063/5.0099294","DOIUrl":null,"url":null,"abstract":"<p><p>The nanoscale organization of functional (bio)molecules on solid substrates with nanoscale spatial resolution and single-molecule control-in both position and orientation-is of great interest for the development of next-generation (bio)molecular devices and assays. Herein, we report the fabrication of nanoarrays of individual proteins (and dyes) via the selective organization of DNA origami on nanopatterned surfaces and with controlled protein orientation. Nanoapertures in metal-coated glass substrates were patterned using focused ion beam lithography; 88% of the nanoapertures allowed immobilization of functionalized DNA origami structures. Photobleaching experiments of dye-functionalized DNA nanostructures indicated that 85% of the nanoapertures contain a single origami unit, with only 3% exhibiting double occupancy. Using a reprogrammed genetic code to engineer into a protein new chemistry to allow residue-specific linkage to an addressable ssDNA unit, we assembled orientation-controlled proteins functionalized to DNA origami structures; these were then organized in the arrays and exhibited single molecule traces. This strategy is of general applicability for the investigation of biomolecular events with single-molecule resolution in defined nanoarrays configurations and with orientational control of the (bio)molecule of interest.</p>","PeriodicalId":72405,"journal":{"name":"Biophysics reviews","volume":null,"pages":null},"PeriodicalIF":2.9000,"publicationDate":"2022-08-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10903486/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biophysics reviews","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1063/5.0099294","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/9/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 0
Abstract
The nanoscale organization of functional (bio)molecules on solid substrates with nanoscale spatial resolution and single-molecule control-in both position and orientation-is of great interest for the development of next-generation (bio)molecular devices and assays. Herein, we report the fabrication of nanoarrays of individual proteins (and dyes) via the selective organization of DNA origami on nanopatterned surfaces and with controlled protein orientation. Nanoapertures in metal-coated glass substrates were patterned using focused ion beam lithography; 88% of the nanoapertures allowed immobilization of functionalized DNA origami structures. Photobleaching experiments of dye-functionalized DNA nanostructures indicated that 85% of the nanoapertures contain a single origami unit, with only 3% exhibiting double occupancy. Using a reprogrammed genetic code to engineer into a protein new chemistry to allow residue-specific linkage to an addressable ssDNA unit, we assembled orientation-controlled proteins functionalized to DNA origami structures; these were then organized in the arrays and exhibited single molecule traces. This strategy is of general applicability for the investigation of biomolecular events with single-molecule resolution in defined nanoarrays configurations and with orientational control of the (bio)molecule of interest.
在固体基底上以纳米级空间分辨率组织功能(生物)分子,并对其位置和方向进行单分子控制,这对于开发新一代(生物)分子设备和检测方法具有重大意义。在此,我们报告了通过在纳米图案表面上选择性组织 DNA 折纸并控制蛋白质取向来制造单个蛋白质(和染料)纳米阵列的情况。利用聚焦离子束光刻技术在金属涂层玻璃基底上绘制了纳米孔,88%的纳米孔可以固定功能化的DNA折纸结构。对染料功能化的 DNA 纳米结构进行的光漂白实验表明,85% 的纳米孔包含一个折纸单元,只有 3% 的纳米孔显示出双层结构。我们利用重新编程的遗传密码,在蛋白质中加入新的化学成分,使残基特异性连接到可寻址的 ssDNA 单元,从而组装出与 DNA 折纸结构功能化的定向控制蛋白质;这些蛋白质随后被组织到阵列中,并显示出单分子痕迹。这种策略普遍适用于在确定的纳米阵列配置中以单分子分辨率研究生物分子事件,并对感兴趣的(生物)分子进行定向控制。