Intein-based biosynthetic incorporation of unlabeled protein tags into isotopically labeled proteins for NMR studies

被引:101
作者
Züger, S
Iwai, H
机构
[1] Univ Saskatchewan, Dept Chem, Saskatoon, SK S7N 5C9, Canada
[2] Univ Saskatchewan, Dept Biochem, Saskatoon, SK S7N 5C9, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
D O I
10.1038/nbt1097
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Segmental isotopic labeling of proteins using protein ligation is a recently established in vitro method for incorporating isotopes into one domain or region of a protein to reduce the complexity of NMR spectra, thereby facilitating the NMR analysis of larger proteins(1-3). Here we demonstrate that segmental isotopic labeling of proteins can be conveniently achieved in Escherichia coli using intein-based protein ligation. Our method is based on a dual expression system that allows sequential expression of two precursor fragments in media enriched with different isotopes. Using this in vivo approach, unlabeled protein tags can be incorporated into isotopically labeled target proteins to improve protein stability and solubility for study by solution NMR spectroscopy.
引用
收藏
页码:736 / 740
页数:5
相关论文
共 30 条
[1]   THE PROGRAM XEASY FOR COMPUTER-SUPPORTED NMR SPECTRAL-ANALYSIS OF BIOLOGICAL MACROMOLECULES [J].
BARTELS, C ;
XIA, TH ;
BILLETER, M ;
GUNTERT, P ;
WUTHRICH, K .
JOURNAL OF BIOMOLECULAR NMR, 1995, 6 (01) :1-10
[2]   Preparation of uniformly labeled NMR samples in Escherichia coli under the tight control of the araBAD promoter:: expression of an archaeal homolog of the RNase P Rpp29 protein [J].
Boomershine, WP ;
Raj, MLS ;
Gopalan, V ;
Foster, MP .
PROTEIN EXPRESSION AND PURIFICATION, 2003, 28 (02) :246-251
[3]  
Christendat D, 2000, NAT STRUCT BIOL, V7, P903
[4]   Protein trans-splicing and cyclization by a naturally split intein from the dnaE gene of Synechocystis species PCC6803 [J].
Evans, TC ;
Martin, D ;
Kolly, R ;
Panne, D ;
Sun, L ;
Ghosh, I ;
Chen, LX ;
Benner, J ;
Liu, XQ ;
Xu, MQ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (13) :9091-9094
[5]   Protein semi-synthesis in living cells [J].
Giriat, I ;
Muir, TW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (24) :7180-7181
[6]   PROCESSING OF MULTIDIMENSIONAL NMR DATA WITH THE NEW SOFTWARE PROSA [J].
GUNTERT, P ;
DOTSCH, V ;
WIDER, G ;
WUTHRICH, K .
JOURNAL OF BIOMOLECULAR NMR, 1992, 2 (06) :619-629
[7]   TIGHT REGULATION, MODULATION, AND HIGH-LEVEL EXPRESSION BY VECTORS CONTAINING THE ARABINOSE P-BAD PROMOTER [J].
GUZMAN, LM ;
BELIN, D ;
CARSON, MJ ;
BECKWITH, J .
JOURNAL OF BACTERIOLOGY, 1995, 177 (14) :4121-4130
[8]   Solution structure of the chitin-binding domain of Bacillus circulans WL-12 chitinase A1 [J].
Ikegami, T ;
Okada, T ;
Hashimoto, M ;
Seino, S ;
Watanabe, T ;
Shirakawa, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (18) :13654-13661
[9]   Strong growth polarity of yeast prion fiber revealed by single fiber imaging [J].
Inoue, Y ;
Kishimoto, A ;
Hirao, J ;
Yoshida, M ;
Taguchi, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (38) :35227-35230
[10]   Cyclic green fluorescent protein produced in vivo using an artificially split PI-PfuI intein from Pyrococcus furiosus [J].
Iwai, H ;
Lingel, A ;
Plückthun, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (19) :16548-16554