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同源肽与基于 DNAzyme 的 ELISA 样测定法结合,用于高特异性和高灵敏度检测纤维蛋白。

Homing peptide combined with DNAzyme-based ELISA-like assay for highly specific and sensitive detection of fibrin.

机构信息

Shandong Provincial Key Laboratory of Chemical Energy Storage and Novel Cell Technology, School of Chemistry and Chemical Engineering, Liaocheng University, Liaocheng, 252000, China.

Shandong Provincial Key Laboratory of Chemical Energy Storage and Novel Cell Technology, School of Chemistry and Chemical Engineering, Liaocheng University, Liaocheng, 252000, China.

出版信息

Talanta. 2022 Feb 1;238(Pt 1):122995. doi: 10.1016/j.talanta.2021.122995. Epub 2021 Oct 28.

DOI:10.1016/j.talanta.2021.122995
PMID:34857328
Abstract

A highly sensitive and specific ELISA-like chemiluminescence method for detection of fibrin has been developed. In the sensing platform, the homing peptide (CREKA), as recognition molecule, which can specially recognize the fibrin on microtiter plate, combined with G-quadruplex-based DNAzyme to form the probe of G-quadruplex-hemin DNAzyme-CREKA. After the sample solution was coated on the plates, the probe was crosslinked with fibrin through the interaction of CREKA and fibrin. Finally, luminol-HO chemiluminesecence (CL) reaction was exploited for quantitative analysis of fibrin. The liner range for fibrin detection was from 0.112 pmol L to 5.6 pmol L with the detection limit of fibrin as low as 0.04 pmol L, based on a signal-to-noise ratio (S/N) of 3. Furthermore, on the basis of the high amplification efficiency of the rolling circle amplification (RCA) reaction, the method enabled to analyze fibrin with a detection limit corresponding to 0.06 fmol L, whose sensitivity increased 3 orders of magnitude than that of above method in the absence of RCA reaction. In particular, combined with the separation and washing steps of ELISA, the proposed method possessed higher selectivity, high-throughput and low cost, which shows promise for applications in clinical diagnosis.

摘要

已经开发出一种用于检测纤维蛋白的高灵敏度和特异性 ELISA 样化学发光方法。在传感平台中,同源肽 (CREKA) 作为识别分子,可以特异性地识别微孔板上的纤维蛋白,与基于 G-四链体的 DNA 酶结合形成 G-四链体-辣根过氧化物酶 DNA 酶-CREKA 探针。将样品溶液涂覆在平板上后,探针通过 CREKA 和纤维蛋白的相互作用与纤维蛋白交联。最后,利用鲁米诺-HO 化学发光 (CL) 反应进行纤维蛋白的定量分析。基于信噪比 (S/N) 为 3,纤维蛋白检测的线性范围为 0.112 pmol L 至 5.6 pmol L,检测限低至 0.04 pmol L。此外,基于滚环扩增 (RCA) 反应的高扩增效率,该方法能够分析检测限低至 0.06 fmol L 的纤维蛋白,其灵敏度比没有 RCA 反应时的方法提高了 3 个数量级。特别是,结合 ELISA 的分离和洗涤步骤,该方法具有更高的选择性、高通量和低成本,有望应用于临床诊断。

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