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HFBI 修饰荧光 ICTS 上低浓度抗体的有效生物活性保留用于 PSA 的灵敏快速检测

Effective Bioactivity Retention of Low-Concentration Antibodies on HFBI-Modified Fluorescence ICTS for Sensitive and Rapid Detection of PSA.

机构信息

School of Life Sciences, Tianjin Engineering Center of Micro-Nano Biomaterials and Detection-Treatment Technology, Collaborative Innovation Center of Chemical Science and Engineering (Tianjin) , Tianjin University , Tianjin 300072 , China.

State Key Laboratory of Chemo/Biosensing and Chemometrics , Hunan University , Changsha 410082 , China.

出版信息

ACS Appl Mater Interfaces. 2018 May 2;10(17):14549-14558. doi: 10.1021/acsami.8b02945. Epub 2018 Apr 18.

Abstract

Nowadays, increasing analytical sensitivity is still a big challenge in constructing membrane-based fluorescence immunochromatography test strips (FICTS). However, the bioactivity of antibody (Ab) immobilized on the test line (T line) of porous nitrocellulose membrane (PNM), which directly influences the analytical sensitivity, is less studied. In this work, a novel amphiphilic hydrophobin (HFBI) protein was introduced to modify the T line to effectively retain the Abs' bioactivity. The results indicated that HFBI could self-assemble on the PNM and immobilize the Abs in the "stand-up" orientation. Compared with the conventional FICTS, the HFBI-modified FICTS with only 0.2 mg/mL of monoclonal Abs on T line enable more accurate quantitative detection and better sensitivity (0.06 ng/mL for prostate specific antigen), which is more than 2 orders of magnitude lower than that of the conventional FICTS with the same concentration of monoclonal Abs on T line. Furthermore, the accuracy of this HFBI-modified FICTS was investigated by testing 150 clinical serum samples and the detection results were coincident with those by electrochemiluminescence immunoassay. Our results provide a novel and promising strategy of Ab immobilization on FICTS for near-patient and point-of-care application.

摘要

如今,提高分析灵敏度仍然是构建基于膜的荧光免疫层析测试条(FICTS)的一大挑战。然而,固定在多孔硝酸纤维素膜(PNM)测试线上的抗体(Ab)的生物活性,直接影响分析灵敏度,却很少被研究。在这项工作中,一种新型的两亲性疏水蛋白(HFBI)被引入来修饰 T 线,以有效地保留 Ab 的生物活性。结果表明,HFBI 可以在 PNM 上自组装,并将 Ab 固定在“直立”状态。与传统的 FICTS 相比,T 线上仅使用 0.2mg/mL 的单克隆 Ab 的 HFBI 修饰的 FICTS 能够进行更准确的定量检测和更好的灵敏度(前列腺特异性抗原为 0.06ng/mL),比 T 线上具有相同浓度的单克隆 Ab 的传统 FICTS 低两个数量级以上。此外,通过测试 150 个临床血清样本,研究了这种 HFBI 修饰的 FICTS 的准确性,检测结果与电化学发光免疫分析的结果一致。我们的结果为基于 FICTS 的 Ab 固定提供了一种新颖且有前途的策略,可用于床边和即时检测。

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