ALKALINE-PHOSPHATASE FUSIONS - SENSORS OF SUBCELLULAR LOCATION

被引:204
作者
MANOIL, C
MEKALANOS, JJ
BECKWITH, J
机构
[1] HARVARD UNIV,SCH MED,DEPT MICROBIOL & MOLEC GENET,BOSTON,MA 02115
[2] UNIV WASHINGTON,DEPT GENET,SEATTLE,WA 98195
关键词
D O I
10.1128/jb.172.2.515-518.1990
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Alkaline phosphatase fusions allow genes to be identified solely on the basis of their protein products being exported from the cytoplasm. Thus, the use of such fusions helps render biological processes which involve cell envelope and secreted proteins accessible to a sophisticated genetic analysis. Furthermore, alkaline phosphatase fusions can be used to locate export signals. Specifying such signals is an important component of studies on the structure of individual cell envelope proteins. The basis of the alkaline phosphatase fusion approach is the finding that the activity of the enzyme responds differently to different environments. Thus, the activity of the fusion protein gives evidence as to its location. This general approach of using sensor proteins which vary in their function, depending on their environment, could be extended to the study of other sorts of problems. It may be that certain enzymes will provide an assay for localization to a particular subcellular compartment, if the environment of the compartment differs from that of others. For instance, the lysosome is more acidic than other intracellular organelles. A gene fusion system employing a reporter enzyme that could show activity only at the pH of the lysosome could allow the detection of signals determining lysosomal localization. Analogous types of enzymes may be used as probes for other subcellular compartments.
引用
收藏
页码:515 / 518
页数:4
相关论文
共 49 条
[1]   TOPOLOGY OF MEMBRANE INSERTION INVITRO AND PLASMA-MEMBRANE ASSEMBLY INVIVO OF THE YEAST ARGININE PERMEASE [J].
AHMAD, M ;
BUSSEY, H .
MOLECULAR MICROBIOLOGY, 1988, 2 (05) :627-635
[2]   TOPOLOGY ANALYSIS OF THE SECY PROTEIN, AN INTEGRAL MEMBRANE-PROTEIN INVOLVED IN PROTEIN EXPORT IN ESCHERICHIA-COLI [J].
AKIYAMA, Y ;
ITO, K .
EMBO JOURNAL, 1987, 6 (11) :3465-3470
[3]   USE OF TNPHOA TO DETECT GENES FOR EXPORTED PROTEINS IN ESCHERICHIA-COLI - IDENTIFICATION OF THE PLASMID-ENCODED GENE FOR A PERIPLASMIC ACID-PHOSPHATASE [J].
BOQUET, PL ;
MANOIL, C ;
BECKWITH, J .
JOURNAL OF BACTERIOLOGY, 1987, 169 (04) :1663-1669
[4]   DETERMINANTS OF MEMBRANE-PROTEIN TOPOLOGY [J].
BOYD, D ;
MANOIL, C ;
BECKWITH, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (23) :8525-8529
[5]   A VECTOR FOR THE CONSTRUCTION OF TRANSLATIONAL FUSIONS TO TEM BETA-LACTAMASE AND THE ANALYSIS OF PROTEIN EXPORT SIGNALS AND MEMBRANE-PROTEIN TOPOLOGY [J].
BROOMESMITH, JK ;
SPRATT, BG .
GENE, 1986, 49 (03) :341-349
[6]   BACTERIAL MOTILITY - MEMBRANE TOPOLOGY OF THE ESCHERICHIA-COLI MOTB PROTEIN [J].
CHUN, SY ;
PARKINSON, JS .
SCIENCE, 1988, 239 (4837) :276-278
[7]   EXPORT OF HYBRID PROTEINS FHUA'-'LACZ AND FHUA'-'PHOA TO THE CELL-ENVELOPE OF ESCHERICHIA-COLI K-12 [J].
COULTON, JW ;
REID, GK ;
CAMPANA, A .
JOURNAL OF BACTERIOLOGY, 1988, 170 (05) :2267-2275
[8]   A GENE FUSION APPROACH TO THE STUDY OF PULLULANASE EXPORT AND SECRETION IN ESCHERICHIA-COLI [J].
DENFERT, C ;
PUGSLEY, AP .
MOLECULAR MICROBIOLOGY, 1987, 1 (02) :159-168
[9]   USE OF A BETA-LACTAMASE FUSION VECTOR TO INVESTIGATE THE ORGANIZATION OF PENICILLIN-BINDING PROTEIN 1B IN THE CYTOPLASMIC MEMBRANE OF ESCHERICHIA-COLI [J].
EDELMAN, A ;
BOWLER, L ;
BROOMESMITH, JK ;
SPRATT, BG .
MOLECULAR MICROBIOLOGY, 1987, 1 (01) :101-106
[10]   IDENTIFICATION AND CHARACTERIZATION OF TNPHOA MUTANTS OF SALMONELLA THAT ARE UNABLE TO PASS THROUGH A POLARIZED MDCK EPITHELIAL-CELL MONOLAYER [J].
FINLAY, BB ;
STARNBACH, MN ;
FRANCIS, CL ;
STOCKER, BAD ;
CHATFIELD, S ;
DOUGAN, G ;
FALKOW, S .
MOLECULAR MICROBIOLOGY, 1988, 2 (06) :757-766