The Key Lab of Analysis and Detection Technology for Food Safety of the Ministry of Education, College of Chemistry, Chemical Engineering, Fuzhou University, Fuzhou 350002, People's Republic of China.
Anal Chem. 2011 Oct 1;83(19):7276-82. doi: 10.1021/ac200617k. Epub 2011 Sep 7.
Peptide-protein interactions have critical roles in biology. Monitoring peptide-protein interactions plays an important role in investigating molecular recognition, screening drugs, and designing biosensors. In this paper, we develop a novel fluorescent approach to monitor peptide-protein interactions based on the assembly of pyrene-labeled peptide and graphene oxide (GO). The pyrene-labeled peptide is strongly adsorbed on the surface of GO via π-π interactions and hydrophobic interactions. As a result, the proximity of the GO to the pyrene moiety effectively quenches the fluorescence of pyrene. In the presence of target protein, the competitive binding of the target protein with GO for peptide results in the restoration of fluorescence signal. This signaling mechanism makes it possible to monitor the peptide-protein interactions in a homogeneous real-time format.
肽-蛋白相互作用在生物学中具有关键作用。监测肽-蛋白相互作用对于研究分子识别、筛选药物和设计生物传感器都具有重要意义。在本文中,我们开发了一种基于芘标记肽和氧化石墨烯(GO)组装的新型荧光方法来监测肽-蛋白相互作用。芘标记肽通过π-π相互作用和疏水相互作用强烈吸附在 GO 表面上。因此,GO 与芘部分的接近有效地猝灭了芘的荧光。在存在靶蛋白的情况下,靶蛋白与 GO 竞争结合肽导致荧光信号恢复。这种信号机制使得以均相实时格式监测肽-蛋白相互作用成为可能。