Hugo J. Rodríguez-Franco, Pauline B. M. Hendrickx and Maartje M. C. Bastings*,
{"title":"Tailoring DNA Origami Protection: A Study of Oligolysine-PEG Coatings for Improved Colloidal, Structural, and Functional Integrity","authors":"Hugo J. Rodríguez-Franco, Pauline B. M. Hendrickx and Maartje M. C. Bastings*, ","doi":"10.1021/acspolymersau.4c0008510.1021/acspolymersau.4c00085","DOIUrl":null,"url":null,"abstract":"<p >Application of protective polymer coatings to enhance the biostability of DNA-based nanomaterials (DONs) has become common practice in <i>in vitro</i> and <i>in vivo</i> experiments. While the functional effect of these coatings is obvious, a detailed molecular picture of what is protected and for how long remains unclear. Additionally, the use of the oligolysine-1kPEG protective polymer has been limited due to aggregation issues. In this study, we evaluated the colloidal stability, structural integrity, and functional preservation of DONs coated with oligolysine (K)-1k/5kPEG block copolymers. Dynamic light scattering and transmission electron microscopy were employed to assess colloidal stability before and after degradation. A FRET-based assay was developed to monitor the directionality of degradation, while quantitative PCR measured the protection of functional DNA handles, crucial for the design of ligand-functionalized DONs. Our results show that K<sub>10</sub>-1kPEG, while prone to aggregation, can offer similar protection against nucleases as K<sub>10</sub>-5kPEG, provided buffer conditions are carefully chosen. Maintaining the colloidal, structural, and functional stability before and after nuclease exposure supports DON applications, particularly at the biointerface. These insights provide valuable guidelines for selecting the most effective protection strategy and enhancing DON functionality across diverse biological environments.</p>","PeriodicalId":72049,"journal":{"name":"ACS polymers Au","volume":"5 1","pages":"35–44 35–44"},"PeriodicalIF":4.7000,"publicationDate":"2024-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/epdf/10.1021/acspolymersau.4c00085","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS polymers Au","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acspolymersau.4c00085","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
摘要
应用保护性聚合物涂层来提高 DNA 纳米材料(DONs)的生物稳定性已成为体外和体内实验中的常见做法。虽然这些涂层的功能效果显而易见,但保护什么以及保护多长时间的详细分子图谱仍不清楚。此外,由于低聚赖氨酸-1kPEG 保护性聚合物的聚集问题,其使用受到了限制。在本研究中,我们评估了涂有寡聚赖氨酸(K)-1k/5kPEG 嵌段共聚物的 DONs 的胶体稳定性、结构完整性和功能性保护。采用动态光散射和透射电子显微镜评估降解前后的胶体稳定性。我们还开发了一种基于 FRET 的检测方法来监测降解的方向性,而定量 PCR 则测量了功能 DNA 手柄的保护情况,这对于配体功能化 DONs 的设计至关重要。我们的研究结果表明,K10-1kPEG 虽然容易发生聚集,但只要仔细选择缓冲条件,就能提供与 K10-5kPEG 类似的抗核酸酶保护。在核酸酶暴露前后保持胶体、结构和功能的稳定性有助于 DON 的应用,尤其是在生物界面的应用。这些见解为选择最有效的保护策略和增强 DON 在各种生物环境中的功能提供了宝贵的指导。
Tailoring DNA Origami Protection: A Study of Oligolysine-PEG Coatings for Improved Colloidal, Structural, and Functional Integrity
Application of protective polymer coatings to enhance the biostability of DNA-based nanomaterials (DONs) has become common practice in in vitro and in vivo experiments. While the functional effect of these coatings is obvious, a detailed molecular picture of what is protected and for how long remains unclear. Additionally, the use of the oligolysine-1kPEG protective polymer has been limited due to aggregation issues. In this study, we evaluated the colloidal stability, structural integrity, and functional preservation of DONs coated with oligolysine (K)-1k/5kPEG block copolymers. Dynamic light scattering and transmission electron microscopy were employed to assess colloidal stability before and after degradation. A FRET-based assay was developed to monitor the directionality of degradation, while quantitative PCR measured the protection of functional DNA handles, crucial for the design of ligand-functionalized DONs. Our results show that K10-1kPEG, while prone to aggregation, can offer similar protection against nucleases as K10-5kPEG, provided buffer conditions are carefully chosen. Maintaining the colloidal, structural, and functional stability before and after nuclease exposure supports DON applications, particularly at the biointerface. These insights provide valuable guidelines for selecting the most effective protection strategy and enhancing DON functionality across diverse biological environments.