...
首页> 外文期刊>Analytical chemistry >alpha-Synuclein-Confocal Nanoscanning (ASYN-CONA), a Bead-Based Assay for Detecting Early-Stage alpha-Synuclein Aggregation
【24h】

alpha-Synuclein-Confocal Nanoscanning (ASYN-CONA), a Bead-Based Assay for Detecting Early-Stage alpha-Synuclein Aggregation

机译:α-突触核蛋白共聚焦纳米镜(Asyn-Cona),用于检测早期α-突触核蛋白聚集的基于珠子的测定

获取原文
获取原文并翻译 | 示例

摘要

alpha-Synuclein fibrils are considered a hallmark of Parkinson's disease and other synucleinopathies. However, small oligomers that formed during the early stages of alpha-synuclein aggregation are thought to be the main toxic species causing disease. The formation of alpha-synuclein oligomers has proven difficult to follow, because of the heterogeneity and transient nature of the species formed. Here, a novel bead-based aggregation assay for monitoring the earliest stages of alpha-synuclein oligomerization, alpha-Synuclein-Confocal Nanoscanning (ASYN-CONA), is presented. The alpha-synuclein A91C single cysteine mutant is modified with a trifunctional chemical tag, which allows simultaneous fluorescent labeling with a green dye (tetramethylrhodamine, TMR) and attachment to microbeads. Beads with bound TMR-labeled alpha-synuclein are then incubated with a red dye (Cy5)-labeled variant of alpha-synuclein A91C, and EtOH (20%) to induce aggregation. Aggregation is detected by confocal scanning imaging, below the equatorial plane of the beads, which is known as the CONA technique. On-bead TMR-labeled alpha-synuclein and aggregated Cy5-labeled alpha-synuclein from the solution are quantitatively monitored in parallel by detection of fluorescent halos or "rings". alpha-Synuclein on-bead oligomerization results in a linear increase of red bead ring fluorescence intensity over a period of 5 h. Total internal reflection fluorescence microscopy was performed on oligomers cleaved from the beads, and it revealed that (i) oligomers are sufficiently stable in solution to investigate their composition, consisting of 6 +/- 1 monomer units, and (ii) oligomers containing a mean of 15 monomers bind Thioflavin-T. Various known inhibitors of alpha-synuclein aggregation were used to validate the ASYN-CONA assay for drug screening. Baicalein, curcumin, and rifampicin showed concentration-dependent inhibition of the alpha-synuclein aggregation and the IC50 (the concentration of the compound at which the maxiumum intensity was reduced by one-half) were calculated.
机译:α-突触核蛋白原纤维被认为是帕金森病和其他孕核视察的标志。然而,在α-突触核蛋白聚集的早期阶段形成的小寡聚体被认为是导致疾病的主要有毒物种。由于所形成的物种的异质性和瞬态性质,α-突触核蛋白低聚物的形成已经难以遵循。这里,提出了一种用于监测最早阶段的α-突触核蛋白寡聚蛋白化,α-突触核蛋白共聚焦纳米阳型(Asyn-Cona)的新型珠子聚集测定。用三官能化学标签修饰α-突触核蛋白A91C单个半胱氨酸突变体,其允许用绿色染料(四甲基吡啶,TMR)同时荧光标记并与微珠附着。然后将具有结合TMR标记的α-突触核蛋白的珠与α-突触核蛋白A91C的红色染料(CY5) - 标记变体,EtOH(20%)孵育以诱导聚集。通过共聚焦扫描成像来检测聚集,下面是珠子的赤道平面,称为CON​​A技术。通过检测荧光光晕或“环”并行地并联地单独地监测来自珠子TMR标记的α-突触核蛋白和聚集的Cy5标记的α-突触核蛋白。 α-突触核蛋白的珠子低聚导致红色珠圈环荧光强度的线性升高在5小时的时间内。在从珠粒切割的低聚物上进行全内反射荧光显微镜,并显示出(i)寡聚体在溶液中足够稳定,以研究由6 +/- 1单体单元组成的组合物,并含有平均值的寡聚体15个单体结合硫蛋白-T。使用各种已知的α-突触核蛋白聚集体的抑制剂来验证药物筛选的Asyn-Cona测定。本颗粒,姜黄素和利福平显示出浓度依赖性依赖性抑制α-突触核蛋白聚集和IC50(计算较大强度减少一半的化合物的浓度)。

著录项

  • 来源
    《Analytical chemistry》 |2019年第9期|共9页
  • 作者单位

    Univ Edinburgh Sch Biol Sci Kings Bldg Edinburgh EH9 3BF Midlothian Scotland;

    Univ Edinburgh Sch Biol Sci Kings Bldg Edinburgh EH9 3BF Midlothian Scotland;

    Univ Edinburgh EaStCHEM Sch Chem Edinburgh EH9 3FJ Midlothian Scotland;

    Univ Edinburgh Sch Biol Sci Kings Bldg Edinburgh EH9 3BF Midlothian Scotland;

    Univ Edinburgh Sch Biol Sci Inst Stem Cell Res MRC Ctr Regenerat Med Edinburgh EH16 4UU Midlothian Scotland;

    Univ Edinburgh Sch Biol Sci Kings Bldg Edinburgh EH9 3BF Midlothian Scotland;

    Univ Edinburgh Sch Biol Sci Inst Stem Cell Res MRC Ctr Regenerat Med Edinburgh EH16 4UU Midlothian Scotland;

    Univ Edinburgh Sch Biol Sci Kings Bldg Edinburgh EH9 3BF Midlothian Scotland;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号