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

被引:187
作者
Bacher, G
Szymanski, WW
Kaufman, SL
Zöllner, P
Blaas, D
Allmaier, G
机构
[1] Univ Vienna, Inst Analyt Chem, A-1090 Vienna, Austria
[2] Univ Vienna, Inst Expt Phys, A-1090 Vienna, Austria
[3] TSI Inc, St Paul, MN 55216 USA
[4] Univ Vienna, Inst Med Biochem, A-1030 Vienna, Austria
来源
JOURNAL OF MASS SPECTROMETRY | 2001年 / 36卷 / 09期
关键词
GEMMA; nano ESI; charge neutralization; mass; spectrometry; noncovalent biocomplex; protein; virus;
D O I
10.1002/jms.208
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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. Copyright (C) 2001 John Wiley & Sons, Ltd.
引用
收藏
页码:1038 / 1052
页数:15
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