Gallego-Villarejo Lucía, Wallin Cecilia, Król Sylwia, Enrich-Bengoa Jennifer, Suades Albert, Aguilella-Arzo Marcel, Gomara María José, Haro Isabel, Wärmlander Sebastian, Muñoz Francisco J, Gräslund Astrid, Perálvarez-Marín Alex
Unit of Biophysics Dept of Biochemistry and Molecular Biology, Institute of Neurosciences, Universitat Autònoma de Barcelona, Facultat de Medicina, 08193 Cerdanyola del Vallés, Catalonia, Spain.
Department of Biochemistry and Biophysics, Stockholm University, Stockholm, Sweden.
Comput Struct Biotechnol J. 2022 Oct 14;20:5672-5679. doi: 10.1016/j.csbj.2022.10.014. eCollection 2022.
Amyloid β-peptide (Aβ) misfolding into β-sheet structures triggers neurotoxicity inducing Alzheimer's disease (AD). Molecules able to reduce or to impair Aβ aggregation are highly relevant as possible AD treatments since they should protect against Aβ neurotoxicity. We have studied the effects of the interaction of dynorphins, a family of opioid neuropeptides, with Aβ the most abundant species of Aβ. Biophysical measurements indicate that Aβ interacts with Big Dynorphin (BigDyn), lowering the amount of hydrophobic aggregates, and slowing down the aggregation kinetics. As expected, we found that BigDyn protects against Aβ aggregates when studied in human neuroblastoma cells by cell survival assays. The cross-interaction between BigDyn and Aβ provides insight into the mechanism of amyloid pathophysiology and may open up new therapy possibilities.
淀粉样β肽(Aβ)错误折叠成β-折叠结构会引发神经毒性,进而导致阿尔茨海默病(AD)。能够减少或削弱Aβ聚集的分子作为可能的AD治疗方法具有高度相关性,因为它们应能预防Aβ神经毒性。我们研究了强啡肽(一类阿片类神经肽)与Aβ(Aβ最丰富的种类)相互作用的影响。生物物理测量表明,Aβ与大强啡肽(BigDyn)相互作用,减少了疏水聚集体的数量,并减缓了聚集动力学。正如预期的那样,通过细胞存活试验在人神经母细胞瘤细胞中进行研究时,我们发现BigDyn可预防Aβ聚集体。BigDyn与Aβ之间的交叉相互作用为淀粉样病理生理学机制提供了见解,并可能开辟新的治疗可能性。