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通过毛细管区带电泳-电喷雾/质谱法获得甲基葡萄糖脂多糖/棕榈酰辅酶A非共价复合物的直接证据。

Direct evidence of methylglucose lipopolysaccharides/palmitoyl-CoA noncovalent complexes by capillary zone electrophoresis-electrospray/mass spectrometry.

作者信息

Tuffal G, Tuong A, Dhers C, Uzabiaga F, Rivière M, Picard C, Puzo G

机构信息

Institut de Pharmacologie et Biologie Structurale, CNRS, Toulouse, France.

出版信息

Anal Chem. 1998 May 1;70(9):1853-8. doi: 10.1021/ac971101r.

Abstract

Mycobacterial methylglucose lipopolysaccharides (MGLPs) play an important regulatory role in the biosynthesis of long-chain fatty acids by forming complexes with neosynthesized acyl-CoA fatty acid derivatives. The MGLPs from Mycobacterium smegmatis were purified by high-performance anion-exchange chromatography and characterized by LSIMS and CE/ESI-MS. We investigated their interaction with palmitoyl-CoA using capillary zone electrophoresis with both direct and indirect UV detection. In the latter mode, the signal of the UV-transparent MGLPs decreased upon addition of increasing amounts of palmitoyl-CoA; while using direct UV detection, the addition of palmitoyl-CoA to the MGLPs revealed characteristic profiles. The major peak was assigned to the noncovalent MGLP/palmitoyl-CoA complex on the basis of its electrophoretic mobility. The abundance of the complex was found to increase until the MGLP/palmitoyl-CoA molar ratio reached a 1/1 stoichiometry. The existence of and the stoichiometry of this complex were assessed by CE/ESI mass spectrum analysis, showing pseudomolecular ions of the MGLP/palmitoyl-CoA complex. These results confirm that CE/ESI-MS is a powerful tool to characterize noncovalent molecular association.

摘要

分枝杆菌甲基葡萄糖脂多糖(MGLPs)通过与新合成的酰基辅酶A脂肪酸衍生物形成复合物,在长链脂肪酸的生物合成中发挥重要的调节作用。耻垢分枝杆菌的MGLPs通过高效阴离子交换色谱法进行纯化,并通过液相二次离子质谱(LSIMS)和毛细管电泳/电喷雾电离质谱(CE/ESI-MS)进行表征。我们使用具有直接和间接紫外检测的毛细管区带电泳研究了它们与棕榈酰辅酶A的相互作用。在后一种模式下,随着棕榈酰辅酶A添加量的增加,紫外线透明的MGLPs的信号降低;而使用直接紫外检测时,向MGLPs中添加棕榈酰辅酶A显示出特征性图谱。根据其电泳迁移率,主要峰被归属于非共价MGLP/棕榈酰辅酶A复合物。发现该复合物的丰度会增加,直到MGLP/棕榈酰辅酶A摩尔比达到1/1化学计量比。通过CE/ESI质谱分析评估了该复合物的存在和化学计量比,显示出MGLP/棕榈酰辅酶A复合物的准分子离子。这些结果证实CE/ESI-MS是表征非共价分子缔合的有力工具。

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