Sequence- and site-specific photodissocniation at 266nm of protonated synthetic polypeptides containing a tryptophanyl residue

被引:36
作者
Oh, JY
Moon, JH
Kim, MS [1 ]
机构
[1] Seoul Natl Univ, Sch Chem, Seoul 151742, South Korea
[2] Seoul Natl Univ, Natl Creat Res Initiat, Ctr Control React Dynam, Seoul 151742, South Korea
关键词
D O I
10.1002/rcm.1679
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Photodissociation at 266 nm of protonated synthetic polypeptides containing a tryptophanyl residue was investigated using a homebuilt tandem time-of-flight mass spectrometer equipped with a matrix-assisted laser desorption/ionization source. Efficient photodissociation of the protonated peptides was demonstrated. Most of the intense peaks in the laser-induced tandem mass spectra were sequence ions. Furthermore, sequence ions due to cleavages at all the peptide bonds were observed; this is a feature of the technique that is particularly useful for peptide sequencing. Fragmentations at both ends of the tryptophanyl residue were especially prevalent, which can be useful for location of the tryptophanyl chromophore in a peptide. Copyright (C) 2004 John Wiley Sons, Ltd.
引用
收藏
页码:2706 / 2712
页数:7
相关论文
共 22 条
[1]   CONTRIBUTIONS OF MASS-SPECTROMETRY TO PEPTIDE AND PROTEIN-STRUCTURE [J].
BIEMANN, K .
BIOMEDICAL AND ENVIRONMENTAL MASS SPECTROMETRY, 1988, 16 (1-12) :99-111
[2]  
BUSCH KL, 1998, MASS SPECTROMETRY MA, P15
[3]   A comparison of negative and positive ion time-of-flight post-source decay mass spectrometry for peptides containing basic residues [J].
Clipston, NL ;
Jai-nhuknan, J ;
Cassady, CJ .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2003, 222 (1-3) :363-381
[4]   TANDEM TIME-OF-FLIGHT MASS-SPECTROMETER [J].
CORNISH, TJ ;
COTTER, RJ .
ANALYTICAL CHEMISTRY, 1993, 65 (08) :1043-1047
[5]   Recent progress in matrix-assisted laser desorption ionization postsource decay [J].
Franzen, J ;
Frey, R ;
Holle, A ;
Kräuter, KO .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2001, 206 (03) :275-286
[6]   193 nm photodissociation of larger multiply-charged biomolecules [J].
Guan, ZQ ;
Kelleher, NL ;
OConnor, PB ;
Aaserud, DJ ;
Little, DP ;
McLafferty, FW .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1996, 157 :357-364
[7]   Optimization of sample preparation for peptide sequencing by MALDI-TOF photofragment mass spectrometry [J].
Hettick, JM ;
McCurdy, DL ;
Barbacci, DC ;
Russell, DH .
ANALYTICAL CHEMISTRY, 2001, 73 (22) :5378-5386
[8]   COLLISION-INDUCED FRAGMENTATION OF (M+H)+IONS OF PEPTIDES - SIDE-CHAIN SPECIFIC SEQUENCE IONS [J].
JOHNSON, RS ;
MARTIN, SA ;
BIEMANN, K .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1988, 86 :137-154
[9]   MATRIX-ASSISTED ULTRAVIOLET-LASER DESORPTION OF NONVOLATILE COMPOUNDS [J].
KARAS, M ;
BACHMANN, D ;
BAHR, U ;
HILLENKAMP, F .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1987, 78 :53-68
[10]   SEQUENCING OF PEPTIDES IN A TIME-OF-FLIGHT MASS-SPECTROMETER - EVALUATION OF POSTSOURCE DECAY FOLLOWING MATRIX-ASSISTED LASER-DESORPTION IONIZATION (MALDI) [J].
KAUFMANN, R ;
KIRSCH, D ;
SPENGLER, B .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1994, 131 :355-385