Park Seonhwa, Park Kiryeon, Na Hee Sam, Chung Jin, Yang Haesik
Department of Chemistry and Chemistry Institute for Functional Materials, Pusan National University, Busan 46241, Korea.
Department of Oral Microbiology, School of Dentistry, Pusan National University, Gyeongsangnam-do 50612, Korea.
Anal Chem. 2021 Apr 6;93(13):5644-5650. doi: 10.1021/acs.analchem.1c00572. Epub 2021 Mar 26.
Indirect detection of in saliva, based on proteolytic cleavage by an Arg-specific gingipain (Arg-gingipain), has traditionally been used for simple, initial diagnosis of periodontitis. To accurately detect using a point-of-care format, development of a simple biosensor that can measure the exact concentration of is required. However, electrochemical detection in saliva is challenging due to the presence of various interfering electroactive species in different concentrations. Here, we report a washing- and separation-free electrochemical biosensor for sensitive detection of in saliva. Glycine-proline-arginine conjugated with 4-aminophenol (AP) was used as an electrochemical substrate for a trypsin-like Arg-gingipain, and glycylglycine was used to increase the Arg-gingipain activity. The electrochemical signal of AP was increased using electrochemical-chemical (EC) redox cycling involving an electrode, AP, and tris(2-carboxyethyl)phosphine, and the electrochemical charge signal was corrected using the initial charge obtained before a 15 min incubation period. The EC redox cycling combined with the matrix-corrected signal facilitated a high and reproducible signal without requiring washing and separation steps. The proteolytic cleavage of the electrochemical substrate was specific to . The calculated detection limit for in artificial saliva was 5 × 10 colony-forming units/mL, and the concentration of in human saliva could be measured. The developed biosensor can be used as an initial diagnosis method to distinguish between healthy people and patients with periodontal diseases.
基于精氨酸特异性牙龈蛋白酶(精氨酸 - 牙龈蛋白酶)的蛋白水解切割作用,对唾液中[具体物质未明确]进行间接检测,传统上一直用于牙周炎的简单初步诊断。为了采用即时检测形式准确检测[具体物质未明确],需要开发一种能够测量其确切浓度的简单生物传感器。然而,由于唾液中存在不同浓度的各种干扰性电活性物质,在唾液中进行电化学检测具有挑战性。在此,我们报告一种无需洗涤和分离的电化学生物传感器,用于灵敏检测唾液中的[具体物质未明确]。与4 - 氨基苯酚(AP)共轭的甘氨酸 - 脯氨酸 - 精氨酸用作类胰蛋白酶精氨酸 - 牙龈蛋白酶的电化学底物,甘氨酰甘氨酸用于提高精氨酸 - 牙龈蛋白酶的活性。利用涉及电极、AP和三(2 - 羧乙基)膦的电化学 - 化学(EC)氧化还原循环增加AP的电化学信号,并使用在15分钟孵育期之前获得的初始电荷校正电化学电荷信号。EC氧化还原循环与基质校正信号相结合,无需洗涤和分离步骤即可促进产生高且可重复的信号。电化学底物的蛋白水解切割对[具体物质未明确]具有特异性。人工唾液中[具体物质未明确]的计算检测限为5×10菌落形成单位/毫升,并且可以测量人类唾液中[具体物质未明确]的浓度。所开发的生物传感器可作为区分健康人和牙周疾病患者的初步诊断方法。