Use of a heterodimeric coiled-coil system for biosensor application and affinity purification

被引:87
作者
Chao, HM
Bautista, DL
Litowski, J
Irvin, RT
Hodges, RS [1 ]
机构
[1] Univ Alberta, Prot Engn Network Ctr Excellence, Heritage Med Res Ctr 713, Edmonton, AB T6G 2S2, Canada
[2] Univ Alberta, Dept Med Microbiol & Infect Dis, Edmonton, AB T6G 2H7, Canada
[3] Univ Alberta, Dept Biochem, MRC, Grp Prot Struc & Funct, Edmonton, AB T6G 2H7, Canada
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 1998年 / 715卷 / 01期
基金
英国医学研究理事会; 加拿大自然科学与工程研究理事会;
关键词
reviews; coiled-coil system; biosensors; affinity purification; proteins; peptides;
D O I
10.1016/S0378-4347(98)00172-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The two-stranded or-helical coiled-coil is now recognized as one of nature's favorite ways of creating a dimerization motif. Based on the knowledge of protein folding studies and de novo design model systems, a novel heterodimeric coiled-coil protein was synthesized. The heterodimeric E/K coiled-coil was constructed with two distinct peptides (E and K) that will spontaneously associate into a full helical coiled-coil structure in solution. Equilibrium CD, NMR and real time biosensor kinetics experiments showed that the E/K coiled-coil is both structurally (Delta G(unfold)=11.3 kcal/mol) and kinetically (K-d approximate to 1 nM) stable in solution at neutral pH. The engineered coiled-coil had been applied as a dimerization and capture domain for biosensor based applications and used in an expression/detection/affinity chromatography system. Specific test examples demonstrated the usefulness of the E/K heterodimeric system in these applications. The universality of coiled-coil as a dimerization motif in nature and our ability to design and synthesize these proteins suggest a wide variety of applications. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:307 / 329
页数:23
相关论文
共 95 条
[1]  
Adamson J. Gordon, 1993, Current Opinion in Biotechnology, V4, P428, DOI 10.1016/0958-1669(93)90008-K
[2]  
AMANTI B, 1994, CURR OPIN GENE DEV, V4, P102
[3]   PH-INDUCED DENATURATION OF PROTEINS - A SINGLE SALT BRIDGE CONTRIBUTES 3-5 KCAL MOL TO THE FREE-ENERGY OF FOLDING OF T4-LYSOZYME [J].
ANDERSON, DE ;
BECKTEL, WJ ;
DAHLQUIST, FW .
BIOCHEMISTRY, 1990, 29 (09) :2403-2408
[4]   INTERACTIONS OF COILED COILS IN TRANSCRIPTION FACTORS - WHERE IS THE SPECIFICITY [J].
BAXEVANIS, AD ;
VINSON, CR .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1993, 3 (02) :278-285
[5]   USE OF ANTIBODY FRAGMENTS IN IMMUNOAFFINITY CHROMATOGRAPHY - COMPARISON OF FV FRAGMENTS, VH FRAGMENTS AND PARALOG PEPTIDES [J].
BERRY, MJ ;
DAVIES, J .
JOURNAL OF CHROMATOGRAPHY, 1992, 597 (1-2) :239-245
[6]  
BIRO ENA, 1975, P 9 FED EUR BIOCH SO, P125
[7]   A natural motif approach to protein design: A synthetic leucine zipper peptide mimics the biological function of the platelet factor 4 protein [J].
Butcher, DJ ;
Kowalska, MA ;
Li, S ;
Luo, ZW ;
Shan, SM ;
Lu, ZX ;
Niewiarowski, S ;
Huang, ZW .
FEBS LETTERS, 1997, 409 (02) :183-187
[8]   IMMUNOLOGIC ADSORBENTS .1. ISOLATION OF ANTIBODY BY MEANS OF A CELLULOSE-PROTEIN ANTIGEN [J].
CAMPBELL, DH ;
LUESCHER, E ;
LERMAN, LS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1951, 37 (09) :575-578
[9]  
Carter P, 1995, J Hematother, V4, P463, DOI 10.1089/scd.1.1995.4.463
[10]  
Cavanagh J., 1996, PROTEIN NMR SPECTROS