Department of Applied Chemistry, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, 113-8656, Japan.
ACS Nano. 2023 Jan 10;17(1):212-220. doi: 10.1021/acsnano.2c06007. Epub 2022 Dec 29.
We developed an on-chip enrichment method based on an aqueous two-phase system of dextran/polyethylene glycol mix, DEX/PEG ATPS, for digital bioassay. Accordingly, we prepared an array device of femtoliter reactors that displays millions of uniformly shaped DEX-rich droplets under a PEG-rich medium. The DEX-rich droplets effectively enriched DNA molecules from the PEG-rich medium. To quantify the enrichment power of the system, we performed a digital bioassay of alkaline phosphatase (ALP). Upon genetically tagging ALP molecules with the DEX-binding domain (DBD) derived from dextransucrase, the ALP molecules were enriched 59-fold in the DEX droplets in comparison to that in a conventional digital bioassay. Subsequently, we performed a Cas13-based digital SARS-CoV-2 RNA detection assay to evaluate the performance of this system for a more practical assay. In this assay, the target RNA molecules bound to the DBD-tagged Cas13 molecules were effectively enriched in the DEX droplets. Consequently, an enrichment factor of 31 was achieved. Enrichment experiments for nonlabeled proteins were also performed to test the expandability of this technique. The model protein, nontagged β-galactosidase, was enriched in DEX droplets containing DBD-tagged antibody, with an enrichment factor of over 100. Thus, this system enabled effective on-chip enrichment of target molecules to enhance the detection sensitivity of digital bioassays without using external instruments or an external power source, which would be applicable for on-site bioassays or portable diagnostic tests.
我们开发了一种基于葡聚糖/聚乙二醇混合双水相体系的芯片富集方法,DEX/PEG ATPS,用于数字生物测定。相应地,我们制备了一种包含数万个体积为飞升级的微反应器的阵列器件,在富含 PEG 的介质中呈现出数百万个形状均匀的富含 DEX 的液滴。富含 DEX 的液滴可有效地从富含 PEG 的介质中浓缩 DNA 分子。为了量化该系统的浓缩能力,我们进行了碱性磷酸酶(ALP)的数字生物测定。通过用来源于葡聚糖蔗糖酶的 DEX 结合域(DBD)对 ALP 分子进行基因标记,与传统的数字生物测定相比,ALP 分子在 DEX 液滴中的富集倍数达到 59 倍。随后,我们进行了基于 Cas13 的数字 SARS-CoV-2 RNA 检测测定,以评估该系统在更实际的测定中的性能。在该测定中,与 DBD 标记的 Cas13 分子结合的靶 RNA 分子有效地在 DEX 液滴中浓缩。因此,实现了 31 倍的富集倍数。还进行了非标记蛋白质的富集实验,以测试该技术的可扩展性。模型蛋白,即未标记的β-半乳糖苷酶,在含有 DBD 标记的抗体的 DEX 液滴中被浓缩,富集倍数超过 100。因此,该系统能够有效地在芯片上对靶分子进行浓缩,从而提高数字生物测定的检测灵敏度,而无需使用外部仪器或外部电源,这将适用于现场生物测定或便携式诊断测试。