Gas-phase basicities for ions from bradykinin and its des-arginine analogues

被引:25
作者
Ewing, NP [1 ]
Pallante, GA [1 ]
Zhang, X [1 ]
Cassady, CJ [1 ]
机构
[1] Miami Univ, Dept Chem & Biochem, Oxford, OH 45056 USA
来源
JOURNAL OF MASS SPECTROMETRY | 2001年 / 36卷 / 08期
关键词
bradykinin; gas-phase basicity; deprotonation reaction; molecular modeling; FT-ICR;
D O I
10.1002/jms.188
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Apparent gas-phase basicities (GB(app)s) for [M + H](+) of bradykinin, des-Arg(1)-bradykinin and des-Arg(9)-bradykinin have been assigned by deprotonation reactions of [M + 2H](2+) in a Fourier transform ion cyclotron resonance mass spectrometer. With a GB(app) of 225.8 +/- 4.2 kcal mol(-1), bradykinin [M + H](+) is the most basic of the ions studied. Ions from des-Arg(1)-bradykinin and des-Arg9-bradykinin have GB(app) values of 222.8 +/- 4.3 kcal mol(-1) and 214.9 +/- 2.3 kcal mol(-1), respectively. One purpose of this work was to determine a suitable reaction efficiency 'break point' for assigning GB(app) values to peptide ions using the bracketing method. An efficiency value of 0.1 (i.e. approximately 10% of all collisions resulting in a deprotonation reaction) was used to assign GB(app)s. Support for this criterion is provided by the fact that our GB(app) values for des-Arg(1)-bradykinin and des-Arg(9)-bradykinin are identical, within experimental error, to literature values obtained using a modified kinetic method. However, the GB(app)s for bradykinin ions from the two studies differ by 10.3 kcal mol(-1). The reason for this is not clear, but may involve conformation differences produced by experimental conditions. The results may be influenced by salt-bridge conformers and/or by conformational changes caused by the use of a proton-bound heterodimer in the kinetic method. Factors affecting the basicities of these peptide ions are also discussed, and molecular modeling is used to provide information on protonation sites and conformations. The presence of two highly basic arginine residues on bradykinin results in its high GB(app), while the basicity of des-Arg(1)-bradykinin ions is increased by the presence of two proline residues at the N-terminus. The proline residue in the second position folds the peptide chain in a manner that increases intramolecular hydrogen bonding to the protonated N-terminal amino group of the proline at the first position. Copyright (C) 2001 John Wiley & Sons, Ltd.
引用
收藏
页码:875 / 881
页数:7
相关论文
共 54 条
[1]   HELIX GEOMETRY IN PROTEINS [J].
BARLOW, DJ ;
THORNTON, JM .
JOURNAL OF MOLECULAR BIOLOGY, 1988, 201 (03) :601-619
[2]   PROTON AFFINITIES OF LYSINE AND HISTIDINE - A THEORETICAL CONSIDERATION OF THE DISCREPANCY BETWEEN EXPERIMENTAL RESULTS FROM THE KINETIC AND BRACKETING METHODS [J].
BLIZNYUK, AA ;
SCHAEFER, HF ;
AMSTER, IJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (12) :5149-5154
[3]   A relationship between the kinetics and thermochemistry of proton transfer reactions in the gas phase [J].
Bouchoux, G ;
Salpin, JY ;
Leblanc, D .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1996, 153 (01) :37-48
[4]   DETERMINATION OF RELATIVE GAS-PHASE BASICITIES BY THE PROTON-TRANSFER EQUILIBRIUM TECHNIQUE AND THE KINETIC METHOD IN A QUADRUPOLE ION-TRAP [J].
BRODBELTLUSTIG, JS ;
COOKS, RG .
TALANTA, 1989, 36 (1-2) :255-260
[5]   CHARMM - A PROGRAM FOR MACROMOLECULAR ENERGY, MINIMIZATION, AND DYNAMICS CALCULATIONS [J].
BROOKS, BR ;
BRUCCOLERI, RE ;
OLAFSON, BD ;
STATES, DJ ;
SWAMINATHAN, S ;
KARPLUS, M .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 1983, 4 (02) :187-217
[6]   A FOURIER TRANSFORM-ION CYCLOTRON-RESONANCE STUDY OF STERIC EFFECTS ON PROTON-TRANSFER REACTIONS OF POLYALKYL BENZENES [J].
BUKER, HH ;
GRUTZMACHER, HF .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1991, 109 :95-104
[7]   Thermal dissociation of gaseous bradykinin ions [J].
Butcher, DJ ;
Asano, KG ;
Goeringer, DE ;
McLuckey, SA .
JOURNAL OF PHYSICAL CHEMISTRY A, 1999, 103 (43) :8664-8671
[8]  
Carr SR, 1997, J MASS SPECTROM, V32, P959
[9]   EXPERIMENTAL AND AB-INITIO STUDIES ON PROTONATIONS OF ALANINE AND SMALL PEPTIDES OF ALANINE AND GLYCINE [J].
CASSADY, CJ ;
CARR, SR ;
ZHANG, K ;
CHUNGPHILLIPS, A .
JOURNAL OF ORGANIC CHEMISTRY, 1995, 60 (06) :1704-1712
[10]   Role of the site of protonation in the low-energy decompositions of gas-phase peptide ions [J].
Cox, KA ;
Gaskell, SJ ;
Morris, M ;
Whiting, A .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1996, 7 (06) :522-531