d-Enantiomeric RTHLVFFARK-NH₂: A Potent Multifunctional Decapeptide Inhibiting Cu²⁺-Mediated Amyloid β-Protein Aggregation and Remodeling Cu²⁺-Mediated Amyloid β Aggregates

Abstract

Aggregation of amyloid β-protein (Aβ) into β-sheet-rich plaques is a general feature of Alzheimer’s disease (AD). Homeostasis dysregulation of Cu2+ mediates Aβ to form high cytotoxic aggregates, which causes cell damage by generation of reactive oxygen species (ROS). To improve the inhibitory potency and explore the multifaceted functions of our previously designed decapeptide, RTHLV­FFARK-NH2 (RK10), we have herein reformulated the decapeptide into its d-enantiomer, rk10, and the effects of chirality on Aβ aggregation, Cu2+-mediated Aβ aggregations, and aggregate-remodeling effects were investigated. The results revealed the following: (1) The d-enantiomer presented enhanced inhibitory potency on Aβ fibrillogenesis in comparison to RK10; rk10 and RK10 increased the cell viability from 60% to 91% and 71%, respectively, at an equimolar concentration to Aβ. (2) The enantiomers were chemically equivalent to Cu2+ chelation, ROS suppression and oxidative damage rescue. (3) The d-enantiomer exhibited higher performance to inhibit Cu2+-mediated Aβ aggregation, and more significantly attenuated the cytotoxicity caused by Aβ42-Cu2+ complex than RK10. Cell viability was rescued from 51% to 89% and 74% by coincubating with rk10 and RK10 at 50 μM, respectively. Intracellular ROS levels generated by Aβ42 and Aβ42-Cu2+ species were also remarkably decreased by treating with rk10. (4) The enantiomers could remodel mature Aβ42-Cu2+ aggregates by Cu2+ chelation, and rk10 showed higher performance than RK10, as evidenced by the enhanced cell viability from 57% to 86% by RK10 and to 96% by rk10. The d-enantiomer also showed higher ability than RK10 on protecting the disrupted species from reaggregation. Taken together, D-chiral derivatization of the decapeptide resulted in a potent multifunctional agent in inhibiting Cu2+-mediated Aβ aggregation and remodeling mature Aβ-Cu2+ species. To the best of our knowledge, this is the first investigation on the chirality effect of a multifunctional peptide inhibitor on Cu2+-mediated Aβ aggregation and on the remodeling effect of mature Aβ-Cu2+ aggregates. The work provides new insights into the critical role of chirality in the multifaceted functions of peptide inhibitors against amyloid formation and its toxicity.

Design of Multifunctional Agent Based on Basified Serum Albumin for Efficient In Vivo β-Amyloid Inhibition and Imaging

“…1−4 The attenuation of Aβ accumulation toward alleviating amyloid-associated neurotoxicity has been considered as a promising therapeutic strategy for AD treatment. Many efforts have been done to develop different agents for inhibiting Aβ fibrillization, such as small organic molecules, 5,6 peptides, 7,8 proteins, 9 and nanoparticles. 10,11 Moreover, the remodeling or disassembly of performed Aβ aggregates has recently attracted wide attention.…”

The Role of Exosomal microRNAs and Oxidative Stress in Neurodegenerative Diseases

“…Reciprocally, Aβ has several pathways to induce cells to overexpress ROS and then increase oxidative stress. For instance, metal ion-chelate Aβ can restore the O 2 through a three-step cycle where O 2 is gradually reduced to superoxide and oxygen peroxide, eventually forming OH radicals and generating ROS as byproducts [34][35][36]. Moreover, Aβ can also directly stimulate oxidative stress through endoplasmic stress, lipid peroxidation, and mitochondria dysfunction [37][38][39].…”

Nanomaterials for Modulating the Aggregation of β-Amyloid Peptides

“…Prompted by the need to pursue effective treatment of AD, many inhibitors against Aβ aggregation and cytotoxicity were explored, including small molecules, peptides [ 17 , 18 , 19 ], proteins [ 20 , 21 , 22 ] and antibodies [ 23 ]. For example, we demonstrated that 5,10,15,20-tetrakis(N-methyl-4-pyridyl)-porphyrin (TMPyP), a water-soluble porphyrin, can inhibit Aβ aggregation, disintegrate the preformed Aβ aggregates and alleviate Aβ-induced cytotoxicity [ 24 ].…”

“…[16][17][18][19][20][21][22] peptide[84]. Moreover,Kim et al reported that a C 60 derivate(1,2-dimethoxymethanofullerene) could bind to the central motif, namely, Aβ 16-20 (KLVFF), based on the strong hydrophobic interaction and inhibit the aggregation of Aβ peptides at the early stage[85].…”