一种通用且高效的分离 DNA-聚合酶缀合物的方法。
A Versatile and Efficient Method to Isolate DNA-Polymer Conjugates.
机构信息
Max Planck Institute for Polymer Research, Ackermannweg 10, 55128 Mainz, Germany.
出版信息
ACS Macro Lett. 2023 Sep 19;12(9):1257-1263. doi: 10.1021/acsmacrolett.3c00371. Epub 2023 Sep 1.
We present a facile and adaptable method to purify and isolate DNA-polymer conjugates from different uncharged homo, random, or block copolymer families. Anion exchange chromatography is used to separate the reaction solution and retrieve the excess unreacted polymer and oligonucleotide. The stationary phase has a high efficiency (25 nmol of DNA per run), facilitating the purification of large batches without compromising the peak shape and resolution. To demonstrate the versatility of this method, different types of polymers, including acrylates, methacrylates, and acrylamides containing hydrophilic and hydrophobic blocks, were purified with high yields. Additionally, DNA-polymer conjugates with various DNA block lengths were also successfully purified, further highlighting the broad applicability of this method.
我们提出了一种简便且适应性强的方法,可从不同的不带电荷的同系物、无规和嵌段共聚物家族中纯化和分离 DNA-聚合物缀合物。阴离子交换色谱用于分离反应溶液并回收过量的未反应聚合物和寡核苷酸。固定相具有高效率(每次运行 25 nmol 的 DNA),便于纯化大量批次,而不会影响峰形和分辨率。为了展示该方法的多功能性,用高收率纯化了不同类型的聚合物,包括含亲水性和疏水性嵌段的丙烯酰胺、甲基丙烯酰胺和丙烯酸酯。此外,还成功地纯化了具有不同 DNA 嵌段长度的 DNA-聚合物缀合物,进一步突出了该方法的广泛适用性。