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去甲哈尔满基质增强了基质辅助激光解吸电离质谱法对内毒素的检测能力,用于同时分析病原体、宿主和载体系统。

Norharmane Matrix Enhances Detection of Endotoxin by MALDI-MS for Simultaneous Profiling of Pathogen, Host, and Vector Systems.

作者信息

Scott Alison J, Flinders Bryn, Cappell Joanna, Liang Tao, Pelc Rebecca S, Tran Bao, Kilgour David P A, Heeren Ron M A, Goodlett David R, Ernst Robert K

机构信息

Department of Microbial Pathogenesis, School of Dentistry, University of Maryland Baltimore, Baltimore, Maryland, USA.

FOM-Institute AMOLF, Amsterdam, The Netherlands Maastricht Multimodal Molecular Imaging Institute (M4I), Maastricht University, Maastricht, The Netherlands.

出版信息

Pathog Dis. 2016 Nov;74(8). doi: 10.1093/femspd/ftw097. Epub 2016 Sep 19.

Abstract

The discovery of novel pathogenic mechanisms engaged during bacterial infections requires the evolution of advanced techniques. Here, we evaluate the dual polarity matrix norharmane (NRM) to improve detection of bacterial lipid A (endotoxin), from host and vector tissues infected with Francisella novicida (Fn). We evaluated NRM for improved detection and characterization of a wide range of lipids in both positive and negative polarities, including lipid A and phospholipids across a range of matrix assisted laser desorption-ionization (MALDI)-coupled applications. NRM matrix improved the limit of detection (LOD) for monophosphoryl lipid A (MPLA) down to picogram-level representing a ten-fold improvement of LOD versus 2,5-dihydroxybenzoic acid (DHB) and 100-fold improvement of LOD versus 9-aminoacridine (9-AA). Improved LOD for lipid A subsequently facilitated detection of the Fn lipid A major ion (m/z 1665) from extracts of infected mouse spleen and the temperature-modified Fn lipid A at m/z 1637 from infected D. variabilis ticks. Finally, we simultaneously mapped bacterial phospholipid signatures within an Fn infected spleen along with exclusively host-derived inositol-based phospholipid (m/z 933) demonstrating co-profiling for the host-pathogen interaction. Expanded use of NRM matrix in other infection models and endotoxin-targeting imaging experiments will improve our understanding of the lipid interactions at the host-pathogen interface.

摘要

发现细菌感染过程中涉及的新致病机制需要先进技术的发展。在此,我们评估双极性基质去甲哈尔满(NRM),以改进对感染新凶手弗朗西斯菌(Fn)的宿主和载体组织中细菌脂多糖(内毒素)的检测。我们评估了NRM在正负两种极性下对多种脂质(包括脂多糖和磷脂)进行改进检测和表征的能力,这些脂质涉及一系列基质辅助激光解吸电离(MALDI)耦合应用。NRM基质将单磷酸脂多糖(MPLA)的检测限(LOD)降低到皮克水平,与2,5 - 二羟基苯甲酸(DHB)相比,检测限提高了10倍,与9 - 氨基吖啶(9 - AA)相比,检测限提高了100倍。脂多糖检测限的提高随后有助于从感染小鼠脾脏提取物中检测到Fn脂多糖主要离子(m/z 1665),以及从感染变异革蜱的提取物中检测到温度修饰的Fn脂多糖(m/z 1637)。最后,我们同时绘制了Fn感染脾脏内的细菌磷脂特征图谱以及仅宿主来源的基于肌醇的磷脂(m/z 933),证明了宿主 - 病原体相互作用的共同分析。在其他感染模型和内毒素靶向成像实验中扩大NRM基质的使用,将增进我们对宿主 - 病原体界面脂质相互作用的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4015/8427938/968ceb29ff94/ftw097fig1.jpg

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