Department ofPharmacy, University ofPatras, Panepistimioupoli, Rion, GR 26504, Greece.
Biopolymers. 2011;96(3):316-27. doi: 10.1002/bip.21558.
Amyloid beta peptide (Abeta) aggregation leads to the senile plaque formation, a process that is strongly influenced by oxidative stress and is considered as the molecular basis of various neurodegenerative diseases, such as Alzheimer's disease (AD). Endogenous antioxidants or dietary derived compounds may down-regulate this process. In this study, the interaction of two antioxidants, oleuropein (OE) and melatonin (M), with Abeta is monitored through nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry. The concerted application of these two analytical techniques provides new experimental evidence and residue-specific insights into the interacting Abeta peptide amino acids that are implicated in this process. Both antioxidant compounds interact in a similar way with the peptide and cause chemical shift variations. The most pronounced resonance changes have been observed for the 1H-15N signals of N-terminal region and Leu17-Phe20 residues, as monitored by NMR titration studies.
β淀粉样肽(Abeta)聚集导致老年斑形成,该过程受氧化应激的强烈影响,被认为是各种神经退行性疾病(如阿尔茨海默病(AD))的分子基础。内源性抗氧化剂或饮食来源的化合物可能会下调该过程。在这项研究中,通过核磁共振(NMR)光谱和质谱监测两种抗氧化剂橄榄苦苷(OE)和褪黑素(M)与 Abeta 的相互作用。这两种分析技术的协同应用为涉及该过程的相互作用 Abeta 肽氨基酸提供了新的实验证据和残基特异性见解。这两种抗氧化化合物以相似的方式与肽相互作用并引起化学位移变化。通过 NMR 滴定研究监测到,N 端区域和 Leu17-Phe20 残基的 1H-15N 信号发生了最明显的共振变化。