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电荷降低的纳米电喷雾电离结合肽、蛋白质、糖蛋白、非共价蛋白质复合物和病毒的差分迁移率分析

Charge-reduced nano electrospray ionization combined with differential mobility analysis of peptides, proteins, glycoproteins, noncovalent protein complexes and viruses.

作者信息

Bacher G, Szymanski W W, Kaufman S L, Zöllner P, Blaas D, Allmaier G

机构信息

Institute for Analytical Chemistry, University of Vienna, Währinger Str. 38, A-1090 Vienna, Austria.

出版信息

J Mass Spectrom. 2001 Sep;36(9):1038-52. doi: 10.1002/jms.208.

Abstract

This study explores the potential of a novel electrospray-based method, termed gas-phase electrophoretic mobility molecular analysis (GEMMA), allowing the molecular mass determination of peptides, proteins and noncovalent biocomplexes up to 2 MDa (dimer of immunglobulin M). The macromolecular ions were formed by nano electrospray ionization (ESI) in the 'cone jet' mode. The multiple charged state of the monodisperse droplets/ions generated was reduced by means of bipolar ionized air (generated by an alpha-particle source) to yield exclusively singly charged positive and negative ions as well as neutrals. These ions are separated subsequently at atmospheric pressure using a nano differential mobility analyzer according to their electrophoretic mobility in air. Finally, the ions are detected using a standard condensation particle counter. Data were expressed as electrophoretic mobility diameters by applying the Millikan equation. The measured electrophoretic mobility diameters, or Millikan diameters, of 32 well-defined proteins were plotted against their molecular weights in the range 3.5 to 1920 kDa and exhibited an excellent squared correlation coefficient (r(2) = 0.999). This finding allowed the exact molecular weight determination of large (glyco)proteins and noncovalent biocomplexes by means of this new technique with a mass accuracy of +/-5.6% up to 2 MDa at the femtomole level. From the molecular masses of the weakly bound, large protein complexes thus obtained, the binding stoichiometry of the intact complex and the complex stability as a function of pH, for example, can be derived. Examples of specific protein complexes, such as the avidin or catalase homo-tetramer, are used to illustrate the potential of the technique for characterization of high-mass biospecific complexes. A discussion of current and future applications of charge-reduced nano ESI GEMMA, such as chemical reaction monitoring (reduction process of immunglobulin G) or size determination of an intact virus, a supramolecular complex, and monitoring of partial dissociation of a human rhinoviruses, is provided.

摘要

本研究探索了一种名为气相电泳迁移率分子分析(GEMMA)的新型基于电喷雾的方法的潜力,该方法可测定分子量高达2 MDa(免疫球蛋白M二聚体)的肽、蛋白质和非共价生物复合物。大分子离子通过“锥喷射”模式的纳米电喷雾电离(ESI)形成。通过双极电离空气(由α粒子源产生)降低产生的单分散液滴/离子的多电荷状态,以仅产生单电荷的正离子、负离子以及中性粒子。随后,这些离子在大气压下使用纳米差动迁移率分析仪根据它们在空气中的电泳迁移率进行分离。最后,使用标准凝结核计数器检测离子。通过应用密立根方程将数据表示为电泳迁移率直径。将32种明确的蛋白质的测量电泳迁移率直径(即密立根直径)与其3.5至1920 kDa范围内的分子量作图,显示出极佳的平方相关系数(r² = 0.999)。这一发现使得通过这种新技术能够在飞摩尔水平上精确测定高达2 MDa的大(糖)蛋白和非共价生物复合物的分子量,质量准确度为±5.6%。由此获得的弱结合大蛋白复合物的分子量,例如,可以推导出完整复合物的结合化学计量以及作为pH函数的复合物稳定性。使用特定蛋白质复合物的实例,如抗生物素蛋白或过氧化氢酶同四聚体,来说明该技术用于表征高质量生物特异性复合物的潜力。本文还讨论了电荷降低型纳米ESI GEMMA当前和未来的应用,如化学反应监测(免疫球蛋白G的还原过程)或完整病毒、超分子复合物的大小测定以及人鼻病毒部分解离的监测。

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