Epitope mapping of antibodies against S-tagged fusion proteins and molecular weight markers

被引:6
作者
Daskalow, Katjana [1 ,2 ]
Boisguerin, Prisca [3 ]
Jandrig, Burkhard [2 ]
Volkmer, Rudolf [3 ]
Micheel, Burkhard [1 ]
Schenk, Joerg A. [1 ,4 ]
机构
[1] Univ Potsdam, Inst Biochem & Biol, D-14476 Golm, Germany
[2] Max Delbruck Ctr Mol Med, Dept Tumor Genet, D-13125 Berlin, Germany
[3] Inst Med Immunol, Charite, D-10115 Berlin, Germany
[4] UP Transfer GmbH, Hydrotec, D-14469 Potsdam, Germany
关键词
monoclonal antibody; hybridoma; molecular weight standard; substitution analysis;
D O I
10.1271/bbb.70406
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
Monoclonal antibodies against S-tagged fusion proteins expressed in pET vectors were generated and further characterized. Most pET vectors contain a 15-meric S-tag as a fusion tag for the detection of recombinant proteins. Two antibodies, G18BA3 and G18BE8, recognized this S-tag in enzyme immunoassay and Western blot. Their epitopes were mapped using peptide array technology and were confirmed to be AAKFERQHMDSPD. This corresponds to the C-terminal region of the S-tag plus additional amino acids P and D, which are also present in most available pET vectors. Amino acid substitution analysis revealed several essential residues for binding. The binding motif was therefore FExxHxDxxD for G18BA3 and AxxFExxH for G18BE8. Since some commercially available protein standards are expressed in pET vectors, G18BA3 and G18BE8 were also found to detect the ladder bands of a molecular weight marker on immunoblot analysis. Both antibodies should be highly useful for the simultaneous detection of recombinant pET vector-expressed fusion proteins and protein molecular weight standards in Western blotting, especially when chemoluminescent detection systems are used.
引用
收藏
页码:346 / 351
页数:6
相关论文
共 13 条
[1]   An improved method for the synthesis of cellulose membrane-bound peptides with free C termini is useful for PDZ domain binding studies [J].
Boisguerin, P ;
Leben, R ;
Ay, B ;
Radziwill, G ;
Moelling, K ;
Dong, LY ;
Volkmer-Engert, R .
CHEMISTRY & BIOLOGY, 2004, 11 (04) :449-459
[2]   Differential effects of short affinity tags on the crystallization of Pyrococcus furiosus maltodextrin-binding protein [J].
Bucher, MH ;
Evdokimov, AG ;
Waugh, DS .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 2002, 58 :392-397
[3]   The SPOT synthesis technique - Synthetic peptide arrays on membrane supports - principles and applications [J].
Frank, R .
JOURNAL OF IMMUNOLOGICAL METHODS, 2002, 267 (01) :13-26
[4]   CONTINUOUS CULTURES OF FUSED CELLS SECRETING ANTIBODY OF PREDEFINED SPECIFICITY [J].
KOHLER, G ;
MILSTEIN, C .
NATURE, 1975, 256 (5517) :495-497
[5]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[6]   Expression and study of recombinant ExoM, a β1-4 glucosyltransferase involved in succinoglycan biosynthesis in Sinorhizobium meliloti [J].
Lellouch, AC ;
Geremia, RA .
JOURNAL OF BACTERIOLOGY, 1999, 181 (04) :1141-1148
[7]   BINDING OF IMMUNOGLOBULINS TO PROTEIN-A AND IMMUNOGLOBULIN LEVELS IN MAMMALIAN SERA [J].
LINDMARK, R ;
THORENTOLLING, K ;
SJOQUIST, J .
JOURNAL OF IMMUNOLOGICAL METHODS, 1983, 62 (01) :1-13
[8]   MOLECULAR-CLONING OF RAT OBESE CDNA AND AUGMENTED GENE-EXPRESSION IN GENETICALLY-OBESE ZUCKER FATTY (FA/FA) RATS [J].
OGAWA, Y ;
MASUZAKI, H ;
ISSE, N ;
OKAZAKI, T ;
MORI, K ;
SHIGEMOTO, M ;
SATOH, N ;
TAMURA, N ;
HOSODA, K ;
YOSHIMASA, Y ;
JINGAMI, H ;
KAWADA, T ;
NAKAO, K .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (03) :1647-1652
[9]   Detection of pET-vector encoded, recombinant S-tagged proteins using the monoclonal antibody ATOM-2 [J].
Park, JH ;
Na, SY ;
Lee, HH ;
Lee, YJ ;
Kim, KL .
HYBRIDOMA, 2001, 20 (01) :17-23
[10]  
Schenk JA, 2004, IN VIVO, V18, P649