Immobilized nitro-avidin and nitro-streptavidin as reusable affinity matrices for application in avidin-biotin technology

被引:49
作者
Morag, E [1 ]
Bayer, EA [1 ]
Wilchek, M [1 ]
机构
[1] WEIZMANN INST SCI, DEPT MEMBRANE RES & BIOPHYS, IL-76100 REHOVOT, ISRAEL
关键词
D O I
10.1006/abio.1996.0514
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Chemically modified forms of egg-white avidin and bacterial streptavidin (termed nitro-avidin and nitro-streptavidin, respectively), in which the binding-site tyrosine was nitrated, were used for several biotechnological applications. The fundamental difference between nitro-avidin and the native protein is that interaction of the modified protein with biotin can be reversed under relatively mild conditions. Consequently, nitro-avidin affinity columns or immobilizing matrices can be reused. Three examples are given to demonstrate the possible uses of such columns: (a) biotinylated protein A was attached to a nitro-avidin affinity column, and immunoglobulin was purified directly from whole rabbit serum; (b) biotinylated transferrin was attached to a nitro-streptavidin column, and anti-transferrin was isolated directly from rabbit anti-serum; and (c) biotinylated beta-glucosidase was immobilized onto a nitro-avidin column and used as an enzyme reactor. In each example, the immobilized biotinylated probe could be released selectively from the column and recovered following its utilization. Reusable nitro-avidin thus provides an easy and attractive reversible form of avidin and thereby serves to expand the versatility of avidin-biotin technology. (C) 1996 Academic Press, Inc.
引用
收藏
页码:257 / 263
页数:7
相关论文
共 26 条
[11]   SINGLE-STEP PURIFICATION OF AVIDIN FROM EGG WHITE BY AFFINITY CHROMATOGRAPHY ON BIOCYTIN-SEPHAROSE COLUMNS [J].
CUATRECASAS, P ;
WILCHEK, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1968, 33 (02) :235-+
[12]  
Green N M, 1975, Adv Protein Chem, V29, P85, DOI 10.1016/S0065-3233(08)60411-8
[13]   PROPERTIES OF SUBUNITS OF AVIDIN COUPLED TO SEPHAROSE [J].
GREEN, NM ;
TOMS, EJ .
BIOCHEMICAL JOURNAL, 1973, 133 (04) :687-698
[15]  
KOHANSKI RA, 1990, METHOD ENZYMOL, V184, P194
[16]   THE USE OF CYANOGEN-BROMIDE AND OTHER NOVEL CYANYLATING AGENTS FOR THE ACTIVATION OF POLYSACCHARIDE RESINS [J].
KOHN, J ;
WILCHEK, M .
APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, 1984, 9 (03) :285-305
[17]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[18]   3-DIMENSIONAL STRUCTURES OF AVIDIN AND THE AVIDIN-BIOTIN COMPLEX [J].
LIVNAH, O ;
BAYER, EA ;
WILCHEK, M ;
SUSSMAN, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (11) :5076-5080
[19]   Reversibility of biotin-binding by selective modification of tyrosine in avidin [J].
Morag, E ;
Bayer, EA ;
Wilchek, M .
BIOCHEMICAL JOURNAL, 1996, 316 :193-199
[20]   3-DIMENSIONAL STRUCTURE OF THE TETRAGONAL CRYSTAL FORM OF EGG-WHITE AVIDIN IN ITS FUNCTIONAL COMPLEX WITH BIOTIN AT 2.7-ANGSTROM RESOLUTION [J].
PUGLIESE, L ;
CODA, A ;
MALCOVATI, M ;
BOLOGNESI, M .
JOURNAL OF MOLECULAR BIOLOGY, 1993, 231 (03) :698-710