Intein-mediated ligation and cyclization of expressed proteins

被引:120
作者
Xu, MQ [1 ]
Evans, TC [1 ]
机构
[1] New England Biolabs Inc, Beverly, MA 01915 USA
关键词
D O I
10.1006/meth.2001.1187
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Protein splicing is a posttranslational processing event that releases an internal protein sequence from a protein precursor. During the splicing process the internal protein sequence, termed an intein, embedded in the protein precursor self-catalyzes its excision and the ligation of the flanking protein regions, termed exteins. The dissection of the splicing pathway, which involves the precise cleavage and formation of peptide bonds, and the identification of key catalytic residues at the splice junctions have led to the modulation of the protein splicing process as a protein engineering tool. Novel strategies have been developed to use intein-catalyzed reactions for the production and manipulation of proteins and peptides. These new approaches have broken down the size limitation barrier of chemical synthetic methods and are less technically demanding. The purpose of this article is to describe how to use self-splicing inteins in protein semisynthesis and backbone cyclization. The first two sections of the article provide a brief review of the distinct chemical steps that underlie protein splicing and intein enabled technology. (C) 2001 Academic Press.
引用
收藏
页码:257 / 277
页数:21
相关论文
共 72 条
[1]   Protein splicing: Its chemistry and biology [J].
Anraku, Y .
GENES TO CELLS, 1997, 2 (06) :359-367
[2]  
Ayers B, 1999, BIOPOLYMERS, V51, P343, DOI 10.1002/(SICI)1097-0282(1999)51:5<343::AID-BIP4>3.0.CO
[3]  
2-W
[4]   Biosynthesis of a head-to-tail cyclized protein with improved biological activity [J].
Camarero, JA ;
Muir, TW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (23) :5597-5598
[5]   Extending the applicability of native chemical ligation [J].
Canne, LE ;
Bark, SJ ;
Kent, SBH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (25) :5891-5896
[6]   Protein splicing in the absence of an intein penultimate histidine [J].
Chen, LX ;
Benner, J ;
Perler, FB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (27) :20431-20435
[7]   Utilizing the C-terminal cleavage activity of a protein splicing element to purify recombinant proteins in a single chromatographic step [J].
Chong, SR ;
Montello, GE ;
Zhang, AH ;
Cantor, EJ ;
Liao, W ;
Xu, MQ ;
Benner, J .
NUCLEIC ACIDS RESEARCH, 1998, 26 (22) :5109-5115
[8]   Protein splicing involving the Saccharomyces cerevisiae VMA intein - The steps in the splicing pathway, side reactions leading to protein cleavage, and establishment of an in vitro splicing system [J].
Chong, SR ;
Shao, Y ;
Paulus, H ;
Benner, J ;
Perler, FB ;
Xu, MQ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (36) :22159-22168
[9]   Protein splicing of the Saccharomyces cerevisiae VMA intein without the endonuclease motifs [J].
Chong, SR ;
Xu, MQ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (25) :15587-15590
[10]   Single-column purification of free recombinant proteins using a self-cleavable affinity tag derived from a protein splicing element [J].
Chong, SR ;
Mersha, FB ;
Comb, DG ;
Scott, ME ;
Landry, D ;
Vence, LM ;
Perler, FB ;
Benner, J ;
Kucera, RB ;
Hirvonen, CA ;
Pelletier, JJ ;
Paulus, H ;
Xu, MQ .
GENE, 1997, 192 (02) :271-281