Formation and characterization of protein-protein complexes in vacuo

被引:62
作者
Wells, JM [1 ]
Chrisman, PA [1 ]
McLuckey, SA [1 ]
机构
[1] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
关键词
D O I
10.1021/ja035051l
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Gas-phase reactions between multiply charged positive and negative protein ions are carried out in a quadrupole ion trap mass spectrometer. The ions react with one another by proton transfer and complex formation. Proton transfer products and complexes are formed via competitive processes in single ion/ion encounters. The relative contributions of proton transfer versus complex formation are dependent upon the charges of the ions as well as other characteristics of the ions yet to be clearly delineated. No fragmentation of covalent bonds of the protein reactants is observed. A model that considers the trajectories associated with ion/ion interactions appears to hold the most promise in accounting for the results. The formation of bound ion/ion orbits appears to play an important role in determining overall reaction kinetics as well as the distribution of ion/ion reaction products. Tandem mass spectrometry is used to compare protein complexes formed in the gas-phase with those formed initially in solution and subsequently liberated by electrospray; it is shown that both forms of complex dissociate similarly, but the complexes formed in the gas phase can retain a "memory" of their method of formation.
引用
收藏
页码:7238 / 7249
页数:12
相关论文
共 91 条
[1]   Measurement of external ion injection and trapping efficiency in the ion trap mass spectrometer and comparison with a predictive model [J].
Appelhans, AD ;
Dahl, DA .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2002, 216 (03) :269-284
[2]   NEW RECOMBINATION MECHANISM - TIDAL TERMOLECULAR IONIC RECOMBINATION [J].
BATES, DR ;
MORGAN, WL .
PHYSICAL REVIEW LETTERS, 1990, 64 (19) :2258-2260
[3]   Mass spectrometry of ribosomes and ribosomal subunits [J].
Benjamin, DR ;
Robinson, CV ;
Hendrick, JP ;
Hartl, FU ;
Dobson, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (13) :7391-7395
[4]   FOURIER-TRANSFORM ELECTROSPRAY INSTRUMENTATION FOR TANDEM HIGH-RESOLUTION MASS-SPECTROMETRY OF LARGE MOLECULES [J].
BEU, SC ;
SENKO, MW ;
QUINN, JP ;
WAMPLER, FM ;
MCLAFFERTY, FW .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1993, 4 (07) :557-565
[5]   Deuterium exchange reactions as a probe of biomolecule structure. Fundamental studies of cas phase H/D exchange reactions of protonated glycine oligomers with D2O, CD3OD, CD3CO2D, and ND3 [J].
Campbell, S ;
Rodgers, MT ;
Marzluff, EM ;
Beauchamp, JL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (51) :12840-12854
[6]   Identification of bacteriophage MS2 coat protein from E-coli lysates via ion trap collisional activation of intact protein ions [J].
Cargile, BJ ;
McLuckey, SA ;
Stephenson, JL .
ANALYTICAL CHEMISTRY, 2001, 73 (06) :1277-1285
[7]   DEPROTONATION REACTIONS OF MULTIPLY PROTONATED UBIQUITIN IONS [J].
CASSADY, CJ ;
WRONKA, J ;
KRUPPA, GH ;
LAUKIEN, FH .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 1994, 8 (05) :394-400
[8]   Collision cross sections of myoglobin and cytochrome c ions with Ne, Ar, and Kr [J].
Chen, YL ;
Collings, BA ;
Douglas, DJ .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1997, 8 (07) :681-687
[9]  
Clemmer DE, 1997, J MASS SPECTROM, V32, P577
[10]   COLLISION CROSS-SECTIONS FOR PROTEIN IONS [J].
COVEY, T ;
DOUGLAS, DJ .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1993, 4 (08) :616-623