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褪黑素与β-淀粉样蛋白具有高亲和力和特异性结合:LC-MS 提供了阿尔茨海默病治疗的新视角。

Melatonin binds with high affinity and specificity to beta-amyloid: LC-MS provides insight into Alzheimer's disease treatment.

机构信息

Department of Clinical Laboratory, The First Affiliated Hospital of Anhui Medical University, Hefei, China.

Department of Clinical Laboratory, Anqing Municipal Hospital, Anqing, China.

出版信息

FEBS Open Bio. 2021 Oct;11(10):2800-2806. doi: 10.1002/2211-5463.13279. Epub 2021 Sep 1.

Abstract

To study the potential relationship between melatonin and beta-amyloid (Abeta), we established a liquid chromatography-mass spectrometry (LC-MS) method to quantitatively analyze melatonin, deuterated isotopes (melatonin-D4), and internal standard 6-iodo-2-(4'-dimethylamino-) phenyl-imidazo(1,2) pyridine (IMPY) under positive (+) mode. The gradient elution was set to 6 min, and the corresponding peak time of melatonin and its isotope melatonin-D4 was 3.14 min, while the peak time for the internal standard IMPY was 3.24 min. Next, we established and optimized the molecule receptor saturation binding assay based on LC-MS to determine the melatonin affinity for beta-amyloid (Abeta). Melatonin showed a high and specific binding for Abeta. The corresponding equilibrium dissociation constant (Kd) of melatonin with Abeta 1-40 and Abeta 1-42 was 814.37 ± 36.62 and 628.33 ± 13.57 nmol·L ; besides, the Kd of melatonin with mixed plaques (1-40 and 1-42) was 461.13 ± 45.37 nmol·L . The results may suggest the potential mechanism of action of MT on Abeta and provide a theoretical basis for the improvement of MT treatment of Alzheimer's disease.

摘要

为了研究褪黑素与β-淀粉样蛋白(Abeta)之间的潜在关系,我们建立了一种液相色谱-质谱(LC-MS)方法,以正(+)模式定量分析褪黑素、氘代同位素(褪黑素-D4)和内标 6-碘-2-(4'-二甲氨基)苯基-咪唑并(1,2)吡啶(IMPY)。梯度洗脱设置为 6 分钟,褪黑素及其同位素褪黑素-D4 的相应峰时间为 3.14 分钟,而内标 IMPY 的峰时间为 3.24 分钟。接下来,我们建立并优化了基于 LC-MS 的分子受体饱和结合测定法,以确定褪黑素与β-淀粉样蛋白(Abeta)的亲和力。褪黑素对 Abeta 表现出高特异性结合。褪黑素与 Abeta 1-40 和 Abeta 1-42 的相应平衡解离常数(Kd)分别为 814.37±36.62 和 628.33±13.57 nmol·L -1 ;此外,褪黑素与混合斑块(1-40 和 1-42)的 Kd 为 461.13±45.37 nmol·L -1 。这些结果可能提示了 MT 对 Abeta 的潜在作用机制,并为改善 MT 治疗阿尔茨海默病提供了理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/019b/8487044/3a6ef326f8f3/FEB4-11-2800-g001.jpg

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