BIFUNCTIONAL ACTIVITY LABELS FOR SELECTION OF FILAMENTOUS BACTERIOPHAGES DISPLAYING ENZYMES

被引:17
作者
VANWETSWINKEL, S
TOUILLAUX, R
FASTREZ, J
MARCHANDBRYNAERT, J
机构
[1] UNIV CATHOLIQUE LOUVAIN,DEPT CHEM,BIOCHIM PHYS & BIOPOLYMERES LAB,B-1348 LOUVAIN,BELGIUM
[2] UNIV CATHOLIQUE LOUVAIN,DEPT CHEM,CHIM PHYS & CRISTALLOG LAB,B-1348 LOUVAIN,BELGIUM
[3] UNIV CATHOLIQUE LOUVAIN,DEPT CHEM,CHIM ORGAN SYNTHESE LAB,B-1348 LOUVAIN,BELGIUM
关键词
PHAGE ENZYME; ACTIVITY LABEL; BETA-LACTAMASE; D; D-CARBOXYPEPTIDASE; ENZYME INHIBITION; BIOTINYL SPACER;
D O I
10.1016/0968-0896(95)00084-T
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Two bifunctional activity labels of beta-lactamases or penicillin binding proteins have been prepared. They feature a penicillin sulfone derivative, i.e. a suicide substrate of serine beta-lactamases, or a penicillin derivative connected to a biotin moiety through a spacer containing a disulfide bridge. The biotinyl spacer 4 was prepared by coupling biotin to epsilon-amino-caproic acid, then to cystamine, and purified by transient protection with t-Boc. The penicillin sulfone inhibitor 13 was prepared by chemoselective sulfonylation of methoxymethyl 6-aminopenicillinate with pentafluorophenoxy- or benzyloxy-carbonylmethylsulfonyl chloride (9), followed by permanganate oxidation. Both direct coupling of the activated ester Wb and indirect coupling of the acid 13c obtained by benzyl ester deprotection, afforded the biotinylated sulfone inhibitor 16. The acid 6 resulting from reaction of the biotinyl spacer 4 with glutaric anhydride was activated as pentafluorophenyl-ester 7 and reacted with 6-aminopenicillanic acid to afford the penicillin binding protein label 18. Selection of the most active beta-lactamase displayed on phage from a mixture containing less active enzymes could be accomplished in three rounds of labeling and affinity chromatography using suicide inhibitor 16.
引用
收藏
页码:907 / 915
页数:9
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