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采用弱阳离子交换预分离和纳升毛细管液相色谱-质谱联用技术对单只蜜蜂组织中的肽apidaecin 1亚型进行灵敏定量分析。

A sensitive quantification of the peptide apidaecin 1 isoforms in single bee tissues using a weak cation exchange pre-separation and nanocapillary liquid chromatography coupled with mass spectrometry.

作者信息

Danihlík Jiří, Šebela Marek, Petřivalský Marek, Lenobel René

机构信息

Department of Biochemistry, Faculty of Science, Palacký University, Šlechtitelů 11, 78379 Olomouc, Czech Republic; Department of Protein Biochemistry and Proteomics, Centre of the Region Haná for Biotechnological and Agricultural Research, Faculty of Science, Palacký University, Šlechtitelů 11, 783 71 Olomouc, Czech Republic.

Department of Protein Biochemistry and Proteomics, Centre of the Region Haná for Biotechnological and Agricultural Research, Faculty of Science, Palacký University, Šlechtitelů 11, 783 71 Olomouc, Czech Republic.

出版信息

J Chromatogr A. 2014 Dec 29;1374:134-144. doi: 10.1016/j.chroma.2014.11.041. Epub 2014 Nov 20.

DOI:10.1016/j.chroma.2014.11.041
PMID:25435459
Abstract

Apidaecins represent an important group of antimicrobial peptides occurring in honey bee hemolymph, where they play an important role as key components of humoral immunity. The present study demonstrates the development of a highly sensitive assay for apidaecin 1 isoforms quantification in the hemolymph or body parts from honey bee individuals. The analytical protocol comprises apidaecins 1 purification and enrichment steps by weak cation-exchange chromatography (WCX) in laboratory-made WCX-Tip microcolumns combined with a desalting step on a reversed-phase sorbent (C8) carried in StageTips. Apidaecin-enriched fraction was analyzed by a reversed-phase based nanoliquid chromatography (C4) separation coupled with high-resolution mass spectrometry. The method performance was validated in its specificity, linearity (0-5pmol), recovery (∼45%), precision (<10% at 0.1pmol), limit of detection (∼50fmol), limit of quantification (0.1pmol) and sample stability. The method was successfully applied to analyze the content of apidaecin 1 isoforms in the following samples: hemolymph - 13.0ng/μL (95% confidence interval of 7.5-18.6ng/μL), thoraxes - 36.2ng/unit (95% CI of 18.9-53.6ng/unit) and heads - 12.9ng/unit (95% CI of 9.1-16.7ng/unit). Freshly emerged bees had apidaecin 1 isoforms levels below the limit of detection. Thus it was possible to use them as a competitive matrix for calibration standards to prevent losses of highly basic apidaecins. This new protocol for apidaecin 1 isoforms quantification represents a promising tool to study the role of apidaecins in honey bee immunity and can be considered as a proof-of-concept for the development of sensitive quantification methods for basic antimicrobial peptides in various organisms.

摘要

蜜蜂防御素是存在于蜜蜂血淋巴中的一类重要抗菌肽,它们作为体液免疫的关键成分发挥着重要作用。本研究展示了一种高灵敏度检测方法的开发,用于定量蜜蜂个体血淋巴或身体部位中的蜜蜂防御素1亚型。分析方案包括在实验室自制的弱阳离子交换色谱(WCX)Tip微柱中通过弱阳离子交换色谱法对蜜蜂防御素1进行纯化和富集步骤,并结合在StageTips中进行的反相吸附剂(C8)脱盐步骤。通过基于反相的纳升液相色谱(C4)分离结合高分辨率质谱对富集了蜜蜂防御素的馏分进行分析。该方法的性能在特异性、线性(0 - 5pmol)、回收率(约45%)、精密度(0.1pmol时<10%)、检测限(约50fmol)、定量限(0.1pmol)和样品稳定性方面得到了验证。该方法成功应用于分析以下样品中蜜蜂防御素1亚型的含量:血淋巴 - 13.0ng/μL(95%置信区间为7.5 - 18.6ng/μL),胸部 - 36.2ng/单位(95%置信区间为18.9 - 53.6ng/单位)和头部 - 12.9ng/单位(95%置信区间为9.1 - 16.7ng/单位)。刚羽化的蜜蜂中蜜蜂防御素1亚型水平低于检测限。因此,可以将它们用作校准标准的竞争基质,以防止高碱性蜜蜂防御素的损失。这种用于蜜蜂防御素1亚型定量的新方案是研究蜜蜂防御素在蜜蜂免疫中作用的一种有前景的工具,并且可以被视为开发各种生物体中碱性抗菌肽灵敏定量方法的概念验证。

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