Zhao Jianwei, Li Cuiping, Ma Guimin, Hao Wenhui, Jia Hongxia
Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of Ministry of Education, Key Laboratory of Analytical Science and Technology of Hebei Province, College of Chemistry and Environment Science, Hebei University Baoding 071002 P. R. China
College of Public Health, Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of Ministry of Education, Hebei University Baoding 071002 P. R. China
RSC Adv. 2018 Nov 19;8(68):38758-38764. doi: 10.1039/c8ra07314g. eCollection 2018 Nov 16.
A novel colorimetric strategy for protein detection was developed based on unmodified gold nanoparticles (AuNPs) and terminal protection from a target protein. A hairpin-structured DNA probe with a biotin modification at the 3' terminus combined with streptavidin (SA) by the high affinity between biotin and SA and resisted degradation from exonucleases III (Exo III), which selectively digested double-stranded DNA from the 3'-terminus. The remaining hairpin DNA lost the capacity to protect AuNPs from salt-induced aggregation, resulting in a color change of AuNPs from red to blue. In the absence of SA, Exo III degraded the hairpin DNA into single-stranded DNA, which adsorbed on the surfaces of AuNPs and prevented aggregation, keeping AuNPs with a red color. The state of AuNP aggregation can be discriminated by colorimetry and also can be measured by UV-vis spectroscopy. Our proposed method provided great selectivity and high sensitivity with a detection limit of 0.24 pmol for SA detection. Moreover, the assay avoided modification, enzymatic amplification and special equipment, and also offered the advantages of being simple, cost-effective, and sensitive. This novel strategy holds great promise for the detection of other proteins by small molecule interactions with proteins.
基于未修饰的金纳米颗粒(AuNPs)以及目标蛋白的末端保护作用,开发了一种用于蛋白质检测的新型比色策略。一种在3'末端带有生物素修饰的发夹结构DNA探针,通过生物素与链霉亲和素(SA)之间的高亲和力与链霉亲和素结合,并抵抗外切核酸酶III(Exo III)的降解,Exo III会从3'末端选择性地消化双链DNA。剩余的发夹DNA失去了保护AuNPs免受盐诱导聚集的能力,导致AuNPs的颜色从红色变为蓝色。在没有SA的情况下,Exo III将发夹DNA降解为单链DNA,单链DNA吸附在AuNPs表面并防止聚集,使AuNPs保持红色。AuNP聚集状态可通过比色法进行区分,也可通过紫外可见光谱法进行测量。我们提出的方法具有很高的选择性和灵敏度,SA检测的检测限为0.24 pmol。此外,该检测方法无需修饰、酶促扩增和特殊设备,还具有操作简单、成本效益高和灵敏度高的优点。这种新策略通过小分子与蛋白质的相互作用检测其他蛋白质具有很大的前景。