Mass spectrometric analysis of combinatorial peptide libraries derived from the tandem repeat unit of MUC2 mucin

被引:3
作者
Schlosser, G
Takáts, Z
Vékey, K
Pócsfalvi, G
Malorni, A
Windberg, E
Kiss, A
Hudecz, F
机构
[1] Hungarian Acad Sci, Chem Res Ctr, H-1025 Budapest, Hungary
[2] Ist Sci Alimentaz, Ctr Spettrometria Massa Proteom & Biomol, Avellino, Italy
[3] Eotvos Lorand Univ, Hungarian Acad Sci, Res Grp Peptide Chem, Budapest, Hungary
关键词
combinatorial chemistry; HPLC-MS; peptide library; mass spectrometry; mucin-2; glycoprotein; portioning-mixing; tandem mass spectrometry;
D O I
10.1002/psc.462
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Four 19-member synthetic peptide libraries, based on the TX(1)TX(2)T epitope motif of the mucin-2 gastrointestinal glycoprotein (MUC2) and ranging in peptide length from dipeptides to 15-mers (XT, TXT, TQTXT and KVTPTPTPTGTQTXT), were synthesized by combinatorial solid phase peptide synthesis using the portioning-mixing combinatorial approach, and analysed by electrospray ionization mass spectrometry at different (1000-10000) resolutions. Most of the components of the individual libraries could be easily identified in a single-stage molecular mass screening experiment. The resolving power of the instrument becomes an important factor above 800-1000 Da molecular mass, when predominantly multiply charged molecular ions are formed. Approaches to the identification of isobars (glutamine/lysine), isomers (leucine/isoleucine) and sequence variations by tandem mass spectrometry, and/or by high-performance liquid chromatography-mass spectrometry are outlined. Copyright (C) 2003 European Peptide Society and John Wiley Sons, Ltd.
引用
收藏
页码:361 / 374
页数:14
相关论文
共 52 条
[1]   Resolving isomeric peptide mixtures: A combined HPLC/ion mobility-TOFMS analysis of a 4000-component combinatorial library [J].
Barnes, CAS ;
Hilderbrand, AE ;
Valentine, SJ ;
Clemmer, DE .
ANALYTICAL CHEMISTRY, 2002, 74 (01) :26-36
[2]   THE CARBOHYDRATE-COMPOSITION OF MUCIN IN COLONIC-CANCER [J].
BOLAND, CR ;
DESHMUKH, GD .
GASTROENTEROLOGY, 1990, 98 (05) :1170-1177
[3]   Combinatorial chemistry. Preparation of phenoxypropanolamines [J].
Bryan, WM ;
Huffman, WF ;
Bhatnagar, PK .
TETRAHEDRON LETTERS, 2000, 41 (36) :6997-7000
[4]   Probing combinatorial library diversity by mass spectrometry [J].
Demirev, PA ;
Zubarev, RA .
ANALYTICAL CHEMISTRY, 1997, 69 (15) :2893-2900
[5]   CHARACTERIZATION OF THE COMPLEXITY OF SMALL-MOLECULE LIBRARIES BY ELECTROSPRAY-IONIZATION MASS-SPECTROMETRY [J].
DUNAYEVSKIY, Y ;
VOUROS, P ;
CARELL, T ;
WINTNER, EA ;
REBEK, J .
ANALYTICAL CHEMISTRY, 1995, 67 (17) :2906-2915
[6]  
Enjalbal C, 2000, MASS SPECTROM REV, V19, P139, DOI 10.1002/1098-2787(200005/06)19:3<139::AID-MAS2>3.3.CO
[7]  
2-J
[8]   ELECTROSPRAY IONIZATION FOR MASS-SPECTROMETRY OF LARGE BIOMOLECULES [J].
FENN, JB ;
MANN, M ;
MENG, CK ;
WONG, SF ;
WHITEHOUSE, CM .
SCIENCE, 1989, 246 (4926) :64-71
[9]  
Furka A, 1999, COMB CHEM HIGH T SCR, V2, P105
[10]   GENERAL-METHOD FOR RAPID SYNTHESIS OF MULTICOMPONENT PEPTIDE MIXTURES [J].
FURKA, A ;
SEBESTYEN, F ;
ASGEDOM, M ;
DIBO, G .
INTERNATIONAL JOURNAL OF PEPTIDE AND PROTEIN RESEARCH, 1991, 37 (06) :487-493