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Shotgun analysis of rough-type lipopolysaccharides using ultraviolet photodissociation mass spectrometry

机译:用紫外光解离质谱法对杂型脂多糖的弹枪分析

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摘要

Detailed structural characterization of intact rough-type lipopolysaccharides (R-LPS) was accomplished using an MS3 strategy consisting of collision-induced dissociation (CID) followed by 193 ultraviolet photodissociation (UVPD) implemented on an Orbitrap Fusion mass spectrometer. Complex mixtures of R-LPS from either E. coli or S. enterica were directly infused into the mass spectrometer using static source nanoESI. An initial CID event performed on an R-LPS precursor produced spectra with abundant ions corresponding to the lipid A and core oligosaccharide (OS) substructures. Comparison of CID spectra of R-LPS ions with varying lipid A and core OS structures verify that lipid A and core OS ions are consistently produced in high abundance. The resulting lipid A and core OS ions were subsequently activated by CID, high-energy collision induced dissociation (HCD), or UVPD. For both the lipid A and core OS substructures, HCD and UVPD produced highly informative complementary spectra, with UVPD of the core OS producing an extensive array of cross-ring cleavage fragments. Successful discernment of E. coli R-LPS structures with isomeric core structures confirmed the degree to which subtle structural differences could be determined using this method.
机译:使用MS 3 策略完成完整的粗糙型脂多糖(R-LPS)的详细结构表征,该策略包括碰撞诱导解离(CID),然后在Orbitrap Fusion上实现193紫外光解离(UVPD)质谱仪。使用静态源nanoESI将来自大肠杆菌或肠炎链球菌的R-LPS的复杂混合物直接注入质谱仪中。在R-LPS前体上执行的初始CID事件产生的光谱具有与脂质A和核心寡糖(OS)子结构相对应的丰富离子。比较具有变化的脂质A和核心OS结构的R-LPS离子的CID光谱可验证,脂质A和核心OS离子始终以高丰度产生。随后,通过CID,高能碰撞诱导离解(HCD)或UVPD激活所得的脂质A和核心OS离子。对于脂质A和核心OS亚结构,HCD和UVPD产生了非常丰富的互补光谱,而核心OS的UVPD则产生了广泛的交叉环裂解片段阵列。具有异构核心结构的大肠杆菌R-LPS结构的成功识别证实了使用此方法可以确定微妙的结构差异的程度。

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