Department of Applied Physics and Materials Science, and ‡Division of Chemistry and Chemical Engineering, California Institute of Technology , 1200 East California Boulevard, Pasadena, California 91125, United States.
ACS Nano. 2013 Oct 22;7(10):9452-60. doi: 10.1021/nn404296k. Epub 2013 Oct 8.
We report on a robust and sensitive approach for detecting protective antigen (PA) exotoxin from Bacillus anthracis in complex media. A peptide-based capture agent against PA was developed by improving a bacteria display-developed peptide into a highly selective biligand through in situ click screening against a large, chemically synthesized peptide library. This biligand was coupled with an electrochemical enzyme-linked immunosorbent assay utilizing nanostructured gold electrodes. The resultant assay yielded a limit of detection of PA of 170 pg/mL (2.1 pM) in buffer, with minimal sensitivity reduction in 1% serum. The powdered capture agent could be stably stored for several days at 65 °C, and the full electrochemical biosensor showed no loss of performance after extended storage at 40 °C. The engineered stability and specificity of this assay should be extendable to other cases in which biomolecular detection in demanding environments is required.
我们报告了一种在复杂介质中检测炭疽芽孢杆菌保护性抗原(PA)外毒素的强大而敏感的方法。通过对一个大型化学合成肽文库进行原位点击筛选,将一种针对 PA 的基于肽的捕获剂从细菌展示开发的肽改进为高选择性的双配体。该双配体与利用纳米结构金电极的电化学酶联免疫吸附测定法偶联。该测定法在缓冲液中的 PA 检测限为 170 pg/mL(2.1 pM),在 1%血清中的灵敏度降低最小。粉末状捕获剂可在 65°C 下稳定储存数天,而经过长时间在 40°C 下储存后,完整的电化学生物传感器性能没有任何损失。该检测方法的工程稳定性和特异性应该可以扩展到其他需要在苛刻环境中进行生物分子检测的情况。