Recombinant production, purification and biochemical characterization of domain 6 of LEKTI:: a temporary Kazal-type-related serine proteinase inhibitor

被引:31
作者
Kreutzmann, P [1 ]
Schulz, A [1 ]
Ständker, L [1 ]
Forssmann, WG [1 ]
Mägert, HE [1 ]
机构
[1] IPF Pharmaceut GMBH, D-30625 Hannover, Germany
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2004年 / 803卷 / 01期
关键词
recombinant production; purification; characterization; LEKTI; domain; 6; serine proteinase inhibitor;
D O I
10.1016/j.jchromb.2003.07.016
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Lympho-epithelial Kazal-type-related inhibitor (LEKTI) is a 15-domain serine proteinase inhibitor which is of pathophysiological relevance for skin diseases and atopy. Domains 2 and 15 of LEKTI contain six cysteine residues and match the Kazal-type inhibitor motif almost exactly. The other 13 domains seem to be Kazal-type derived but lack the cysteines in positions 3 and 6 usually conserved within this family of inhibitors. Here, we report the recombinant production and comprehensive biochemical characterization of the 7.7 kDa LEKTI domain 6 (LD-6). Testing a selected number of different serine proteinases, we show that both native and recombinant LD-6 exhibit a significant but temporary inhibitory activity on trypsin. Furthermore, the relation of LEKTI domain 6 to Kazal-type inhibitors is confirmed by determining its disulfide bond pattern (1-4/2-3) and its P, site located after the second Cys residue of LD-6. The established strategy for the recombinant production of LEKTI domain 6 will enable further investigation of its mode of action and its physiological role. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:75 / 81
页数:7
相关论文
共 27 条
[1]   NATURAL PROTEIN PROTEINASE-INHIBITORS AND THEIR INTERACTION WITH PROTEINASES [J].
BODE, W ;
HUBER, R .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 204 (02) :433-451
[2]   Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome [J].
Chavanas, S ;
Bodemer, C ;
Rochat, A ;
Hamel-Teillac, D ;
Ali, M ;
Irvine, AD ;
Bonafé, JL ;
Wilkinson, J ;
Taïeb, A ;
Barrandon, Y ;
Harper, JI ;
de Prost, Y ;
Hovnanian, A .
NATURE GENETICS, 2000, 25 (02) :141-142
[3]   The PROSITE database, its status in 2002 [J].
Falquet, L ;
Pagni, M ;
Bucher, P ;
Hulo, N ;
Sigrist, CJA ;
Hofmann, K ;
Bairoch, A .
NUCLEIC ACIDS RESEARCH, 2002, 30 (01) :235-238
[4]  
GREENE LJ, 1969, J BIOL CHEM, V244, P2646
[5]   RECENT DEVELOPMENTS IN HETEROLOGOUS PROTEIN-PRODUCTION IN ESCHERICHIA-COLI [J].
HOCKNEY, RC .
TRENDS IN BIOTECHNOLOGY, 1994, 12 (11) :456-463
[6]   Determination of the disulfide bond pattern of the endogenous and recombinant angiogenesis inhibitor endostatin by mass spectrometry [J].
John, H ;
Forssmann, WG .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2001, 15 (14) :1222-1228
[7]   ISOLATION OF A CRYSTALLINE TRYPSIN INHIBITOR-ANTICOAGULANT PROTEIN FROM PANCREAS [J].
KAZAL, LA ;
SPICER, DS ;
BRAHINSKY, RA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1948, 70 (09) :3034-3040
[8]   PROTEIN INHIBITORS OF PROTEINASES [J].
LASKOWSKI, M ;
KATO, I .
ANNUAL REVIEW OF BIOCHEMISTRY, 1980, 49 :593-626
[9]   What can the structures of enzyme-inhibitor complexes tell us about the structures of enzyme substrate complexes? [J].
Laskowski, M ;
Qasim, MA .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 2000, 1477 (1-2) :324-337
[10]   Accurate disulfide formation in Escherichia coli:: Overexpression and characterization of the first domain (HF6478) of the multiple Kazal-type inhibitor LEKTI [J].
Lauber, T ;
Marx, UC ;
Schulz, A ;
Kreutzmann, P ;
Rösch, P ;
Hoffmann, S .
PROTEIN EXPRESSION AND PURIFICATION, 2001, 22 (01) :108-112