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采用液相色谱-电喷雾电离-离子阱串联质谱法(LC-ESI-IT-MS/MS)对伊朗蜜蜂(Apis mellifera meda)毒液中的蜂毒肽进行定量分析。

Quantification of Melittin in Iranian Honey Bee (Apis mellifera meda) Venom by Liquid Chromatography-electrospray Ionization-ion Trap Tandem Mass Spectrometry (LC-ESI-IT-MS/MS).

作者信息

Hematyar M, Es-Haghi A, Soleimani M

机构信息

Department of Chemistry, Imam Khomeini International University (IKIU), Qazvin, Iran.

Department of Physico Chemistry, Razi Vaccine and Serum Research Institute, Agricultural Research, Education and Extension Organization (AREEO), Karaj, Iran.

出版信息

Arch Razi Inst. 2019 Dec;74(4):435-439. doi: 10.22092/ari.2018.122150.1219. Epub 2019 Dec 1.

DOI:10.22092/ari.2018.122150.1219
PMID:31939261
Abstract

The current research aimed to quantify melittin (MEL) in Iranian honey bee (Apis mellifera meda) venom. To this end, a liquid chromatography-electrospray ionization-ion trap tandem mass spectrometry (LC-ESI-IT-MS/MS) approach was employed. Melittin is the main toxic peptide of honey bee venom with various biological and pharmacological activities. It was extracted with pure water from the bee venom samples. The analyses were performed on XBridge BEH300 C4 column using a gradient method with the mobile phase consisting of ultrapure water and acetonitrile (containing 0.1% formic acid). Signals of the melittin were recorded with the selected reaction monitoring (SRM) mode, which is a quantitative approach capable of quantifying analyte peptides with high sensitivity and. The mass spectrum of MEL was obtained in the positive ion mode and the quantification analysis was performed using precursor to product ion transition of m/z 570.2/669.9. This method demonstrated good linearity (R2˃0.997) in the range of 1-100 µg mL-1, with a limit of quantification (LOQ) of 1.0 µg mL-1. The content of MEL in Iranian honey bee venom accounts for 43–55% of total dry weight. This method can be used to evaluate the quality and authenticity of bee venom samples for different therapeutic applications of MEL.

摘要

当前的研究旨在对伊朗蜜蜂(西方蜜蜂中东亚种)毒液中的蜂毒肽(MEL)进行定量分析。为此,采用了液相色谱-电喷雾电离-离子阱串联质谱(LC-ESI-IT-MS/MS)方法。蜂毒肽是蜜蜂毒液的主要毒性肽,具有多种生物学和药理活性。它是从蜜蜂毒液样品中用纯水提取的。分析在XBridge BEH300 C4柱上进行,采用梯度法,流动相由超纯水和乙腈(含0.1%甲酸)组成。蜂毒肽的信号通过选择反应监测(SRM)模式记录,这是一种能够高灵敏度定量分析物肽的定量方法。MEL的质谱在正离子模式下获得,定量分析使用m/z 570.2/669.9的前体到产物离子跃迁进行。该方法在1-100μg mL-1范围内显示出良好的线性(R2˃0.997),定量限(LOQ)为1.0μg mL-1。伊朗蜜蜂毒液中MEL的含量占总干重的43-55%。该方法可用于评估用于MEL不同治疗应用的蜜蜂毒液样品的质量和真伪。

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