School of Biology and Biological Engineering, South China University of Technology, Guangzhou, 510006, China.
National Engineering Laboratory of Rapid Diagnostic Tests, Guangzhou Wondfo Biotech Co., Ltd., Guangzhou, 510663, China.
Mikrochim Acta. 2023 Dec 19;191(1):39. doi: 10.1007/s00604-023-06109-y.
Rapid and sensitive dengue non-structural protein 1 (NS1) detection assay is essential for the treatment of disease and currently releases high medical cost burdens. To address the limitations of conventional LFIA strips, we have developed an improved Sup35NM-Z-based LFIA that immobilizes antibodies on cellulose membranes in an orientated manner to increase the sensitivity of LFIA strips. A dual-functional Sup35NM nanofibril was fabricated by fusion with the antibody binding domain; resultant nanofibril from the amyloid Sup35NM was sprayed on the T-line to orientate the capture antibody and produces fluorescence signals. Antibody binding analysis showed that self-assembly of the Sup35NM monomer does not affect the binding activity of the Z-domain with the antibody. The NS1 for DENV-2 infection was chosen as a model target antigen to assess the feasibility of the Sup35NM-Z-domain-based LFIA platform. Under optimal conditions, the Sup35NM-Z-domain-based LFIA detected NS1 within 15 min with a detection limit of 1.29 ng/ml, while the detection limit of traditional LFIA with the same concentration of anti-NS1-Ab1 on the T-line by conventional physical adsorption was 2.20 ng/ml, 1.7 times higher than that of Sup35NM-Z-domain-based LFIA. As compared to traditional LFIAs, the Sup35NM-Z-based LFIA had a wide detection range of 1.29-625 ng/mL. The LFIA's clinical performance in identifying NS1 was also assessed using 15 clinical samples. The LFIA accurately recognized positive and negative samples, equal to 86.7% accuracy. The developed Sup35NM-Z-domain-based LFIA in this study offers great potential for the identification of target markers because of its greatly improved sensitivity and wider detection range.
快速灵敏的登革热非结构蛋白 1(NS1)检测对于疾病的治疗至关重要,目前这会带来高昂的医疗费用负担。为了解决传统 LFIA 条带的局限性,我们开发了一种改良的基于 Sup35NM-Z 的 LFIA,它将抗体定向固定在纤维素膜上,以提高 LFIA 条带的灵敏度。通过与抗体结合域融合,制备了具有双重功能的 Sup35NM 纳米纤维;从淀粉样 Sup35NM 中得到的纳米纤维被喷涂在 T 线上,以定向捕获抗体并产生荧光信号。抗体结合分析表明,Sup35NM 单体的自组装不会影响 Z 结构域与抗体的结合活性。选择 DENV-2 感染的 NS1 作为模型靶标抗原,评估基于 Sup35NM-Z 结构域的 LFIA 平台的可行性。在最佳条件下,基于 Sup35NM-Z 结构域的 LFIA 在 15 分钟内检测到 NS1,检测限为 1.29ng/ml,而传统 LFIA 采用相同浓度的抗 NS1-Ab1 通过传统物理吸附在 T 线上的检测限为 2.20ng/ml,是基于 Sup35NM-Z 结构域的 LFIA 的 1.7 倍。与传统 LFIA 相比,基于 Sup35NM-Z 的 LFIA 的检测范围更宽,为 1.29-625ng/ml。还使用 15 个临床样本评估了 LFIA 对 NS1 的临床性能。LFIA 准确识别阳性和阴性样本,准确率为 86.7%。本研究开发的基于 Sup35NM-Z 的 LFIA 具有极大的灵敏度和更宽的检测范围,因此在识别靶标标志物方面具有很大的潜力。