Highly efficient expression and purification system of small-size protein domains in Escherichia coli for biochemical characterization

Protein Expression and Purification - Tập 47 Số 2 - Trang 599-606 - 2006
Wen-Jing Bao1,2, Yong‐Guang Gao1, Yong-Gang Chang1, Tie-Ying Zhang1, Xiao-Jing Lin1, Xian-Zhong Yan3, Hong Hu1
1Key Laboratory of Proteomics, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China
2School of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Shenyang 110016, China
3NMR Laboratory, National Center of Biomedical Analysis, 27 Taiping Road, Beijing 100850, China

Tóm tắt

Từ khóa


Tài liệu tham khảo

Guan, 1991, Eukaryotic proteins expressed in Escherichia coli: an improved thrombin cleavage and purification procedure of fusion proteins with glutathione S-transferase, Anal. Biochem., 192, 262, 10.1016/0003-2697(91)90534-Z

Guan, 1988, Vectors that facilitate the expression and purification of foreign peptides in Escherichia coli by fusion to maltose-binding protein, Gene, 67, 21, 10.1016/0378-1119(88)90004-2

LaVallie, 1993, A thioredoxin gene fusion expression system that circumvents inclusion-body formation in the E. coli cytoplasm, Biotechnology, 11, 187, 10.1038/nbt0293-187

Tenno, 2004, High-throughput construction method for expression vector of peptides for NMR study suited for isotopic labeling, Protein Eng. Des. Sel., 174, 305, 10.1093/protein/gzh044

Lindhout, 2003, High-yield expression of isotopically labeled peptides for use in NMR studies, Protein Sci., 12, 1786, 10.1110/ps.0376003

Jones, 2000, Expression and membrane assembly of a transmembrane region from Neu, Biochemistry, 39, 1870, 10.1021/bi992495e

Sharon, 2002, Expression, purification, and isotope labeling of a gp120 V3 peptide and production of a Fab from a HIV-1 neutralizing antibody for NMR studies, Prot. Exp. Purif., 24, 374, 10.1006/prep.2001.1577

Gronenborn, 1991, A novel, highly stable fold of the immunoglobulin binding domain of streptococcal protein G, Science, 253, 657, 10.1126/science.1871600

Cheng, 2004, An efficient system for small protein expression and refolding, Biochem. Biophys. Res. Commun., 317, 401, 10.1016/j.bbrc.2004.03.068

Burns, 2000, Tollip, a new component of the IL-1RI pathway, links IRAK to the IL-1 receptor, Nat. Cell Biol., 2, 346, 10.1038/35014038

Faber, 1998, Huntingtin interacts with a family of WW domain proteins, Hum. Mol. Genet., 7, 1463, 10.1093/hmg/7.9.1463

Hofmann, 2001, A ubiquitin-interacting motif conserved in components of the proteasomal and lysosomal protein degradation systems, Trends Biochem. Sci., 26, 347, 10.1016/S0968-0004(01)01835-7

Shimada, 1991, Cloning and expression of a cocaine-sensitive dopamine transporter complementary DNA, Science, 254, 576, 10.1126/science.1948034

Miake, 2002, Biochemical characterization of the core structure of alpha-synuclein filaments, J. Biol. Chem., 277, 19213, 10.1074/jbc.M110551200

Higucchi, 1988, A general method of in vitro preparation and specific mutagenesis of DNA fragments: study of protein and DNA interactions, Nucleic Acids Res., 16, 7351, 10.1093/nar/16.15.7351

Zhou, 2001, A solubility-enhancement tag (SET) for NMR studies of poorly behaving proteins, J. Biomol. NMR, 20, 11, 10.1023/A:1011258906244