College of Environmental Science and Engineering, Anhui Normal University, Wuhu 241000, PR China; Anhui Provincial Engineering Laboratory of Water and Soil Pollution Control and Remediation, Anhui Normal University, Wuhu 241000, PR China.
College of Environmental Science and Engineering, Anhui Normal University, Wuhu 241000, PR China; Anhui Provincial Engineering Laboratory of Water and Soil Pollution Control and Remediation, Anhui Normal University, Wuhu 241000, PR China.
Biosens Bioelectron. 2018 May 30;106:111-116. doi: 10.1016/j.bios.2018.01.069. Epub 2018 Feb 1.
The present study develops a rapid, simple and efficient method for the determination of type IV collagenase by using a specific peptide-modified quartz crystal microbalance (QCM). A small peptide (P1), contains a specific sequence (Pro-Gly) and a terminal cysteine, was synthetized and immobilized to the surface of QCM electrode via the reaction between Au and thiol of the cysteine. The peptide bond between proline and glycine can be specific hydrolyzed cleavage by type IV collagenase, which enabled the modified electrode with a high selectivity toward type IV collagenase. The cleaving process caused a frequency change of QCM to give a signal related to the concentration of type IV collagenase. The morphologies of the modified electrodes were characterized by scanning electron microscope (SEM) and the specific hydrolyzed cleavage process was monitored by QCM. When P1 was modified with gold nanoparticles (P1-Au NPs), the signal could be amplified to further enhance the sensitivity of the designed sensor due to the high-mass of the modified Au NPs. Compared the direct unamplified assay, the values obtained for the limit of detection for type IV collagenase was 0.96 ng mL, yielding about 6.5 times of magnitude improvement in sensitivity. This signal enhanced peptide based QCM biosensor for type IV collagenase also showed good selectivity and sensitivity in complex matrix.
本研究开发了一种快速、简单、高效的方法,通过使用特定的肽修饰石英晶体微天平(QCM)来测定 IV 型胶原酶。合成了一个小肽(P1),包含一个特定的序列(Pro-Gly)和一个末端半胱氨酸,通过 Au 与半胱氨酸的巯基之间的反应固定在 QCM 电极的表面。脯氨酸和甘氨酸之间的肽键可以被 IV 型胶原酶特异性水解切割,这使得修饰电极对 IV 型胶原酶具有高选择性。切割过程导致 QCM 的频率发生变化,从而产生与 IV 型胶原酶浓度相关的信号。通过扫描电子显微镜(SEM)对修饰电极的形貌进行了表征,并通过 QCM 监测了特定的水解切割过程。当 P1 被金纳米粒子(P1-Au NPs)修饰时,由于修饰的 Au NPs 的高质量,可以放大信号,从而进一步提高设计传感器的灵敏度。与直接未放大的测定相比,用于 IV 型胶原酶的检测限的测定值为 0.96ng/mL,灵敏度提高了约 6.5 倍。这种基于信号增强肽的 QCM 生物传感器对 IV 型胶原酶也表现出良好的选择性和灵敏度,在复杂基质中也有很好的表现。