Laboratoire des biomolécules, LBM, Département de chimie, Ecole normale supérieure, PSL University, Sorbonne université, CNRS, 75005 Paris, France.
Dalton Trans. 2020 Feb 21;49(7):2323-2330. doi: 10.1039/c9dt04619d. Epub 2020 Feb 5.
A superoxide dismutase mimic (Mn1) was functionalized with three positively charged-peptides: RRRRRRRRR (Mn1-R9), RRWWWRRWRR (Mn1-RW9) or F-r-F-K (Mn1-MPP). Characterization of the physico-chemical properties of the complexes show that they share similar binding affinity for Mn, apparent reduction potential and intrinsic superoxide dismutase activity. However, their accumulation in cells is different (Mn1-R9 < Mn1-MPP < Mn1-RW9 < Mn1), as well as their subcellular distribution. In addition, the three functionalized-complexes display a better anti-inflammatory activity than Mn1 when assayed at 10 μM. This improvement is due to a combination of an anti-inflammatory effect of the peptidyl moiety itself, and of the SOD mimic for Mn1-RW9 and Mn1-MPP. In contrast, the enhanced anti-inflammatory activity of Mn1-R9 is solely due to the SOD mimic.
一种超氧化物歧化酶模拟物(Mn1)被三个带正电荷的肽基化:RRRRRRRR(Mn1-R9)、RRWWWRRWRR(Mn1-RW9)或 F-r-F-K(Mn1-MPP)。这些配合物的物理化学性质的表征表明,它们对 Mn 的结合亲和力、表观还原电位和固有超氧化物歧化酶活性相似。然而,它们在细胞中的积累情况不同(Mn1-R9 < Mn1-MPP < Mn1-RW9 < Mn1),亚细胞分布也不同。此外,当在 10 μM 下进行测定时,这三种功能化复合物显示出比 Mn1 更好的抗炎活性。这种改善是由于肽段本身的抗炎作用,以及 Mn1-RW9 和 Mn1-MPP 的 SOD 模拟物的结合作用。相比之下,Mn1-R9 增强的抗炎活性仅归因于 SOD 模拟物。