Asymmetric orientation of a phage coat protein in cytoplasmic membrane of Escherichia coli
- PMID: 54916
- PMCID: PMC388808
- DOI: 10.1073/pnas.72.12.4749
Asymmetric orientation of a phage coat protein in cytoplasmic membrane of Escherichia coli
Abstract
The coat protein of a filamentous phage (M13) enters the cytoplasmic membrane from two directions: from the outside upon infection and from the cell interior late in the viral life cycle prior to phage assembly and extrusion. Binding of 125I-labeled anti-coat protein antibody to spheroplasts or to inverted vesicles was used to assay the orientation of coat protein in the membrane. Both parental and newly synthesized coat protein were found to be exposed on the outer surface of the cytoplasmic membrane. Coat protein in intact infected cells is also accessible to external antibody. Thus two different processes of assembling a protein into membrane, each starting from a different membrane surface, appear to produce similar surface orientations.
Similar articles
-
Fractionation of membrane vesicles from coliphage M13-infected Escherichia coli.J Bacteriol. 1976 Jul;127(1):162-7. doi: 10.1128/jb.127.1.162-167.1976. J Bacteriol. 1976. PMID: 132427 Free PMC article.
-
Asymmetric orientation of phage M13 coat protein in Escherichia coli cytoplasmic membranes and in synthetic lipid vesicles.Proc Natl Acad Sci U S A. 1976 Apr;73(4):1159-63. doi: 10.1073/pnas.73.4.1159. Proc Natl Acad Sci U S A. 1976. PMID: 772680 Free PMC article.
-
The orientation of the major coat protein of bacteriophage f1 in the cytoplasmic membrane of Escherichia coli.J Biol Chem. 1981 Oct 10;256(19):9951-8. J Biol Chem. 1981. PMID: 7024275
-
Location of filamentous phage minor coat proteins in phage and in infected cells.J Mol Biol. 1995 Jul 21;250(4):496-506. doi: 10.1006/jmbi.1995.0393. J Mol Biol. 1995. PMID: 7616570
-
Structural constraints on the display of foreign peptides on filamentous bacteriophages.Gene. 1993 Jun 15;128(1):5-11. doi: 10.1016/0378-1119(93)90146-t. Gene. 1993. PMID: 8508959 Review.
Cited by
-
Analysis of time-resolved fluorescence anisotropy in lipid-protein systems. II. Application to tryptophan fluorescence of bacteriophage M13 coat protein incorporated in phospholipid bilayers.Eur Biophys J. 1990;18(5):285-93. doi: 10.1007/BF00188041. Eur Biophys J. 1990. PMID: 2369871
-
Lactoperoxidase-125I localization of salt-extractable alkaline phosphatase on the cytoplasmic membrane of Bacillus licheniformis.J Bacteriol. 1981 Feb;145(2):934-45. doi: 10.1128/jb.145.2.934-945.1981. J Bacteriol. 1981. PMID: 7462164 Free PMC article.
-
Soluble precursor of an integral membrane protein: synthesis of procoat protein in Escherichia coli infected with bacteriophage M13.Proc Natl Acad Sci U S A. 1979 Mar;76(3):1199-203. doi: 10.1073/pnas.76.3.1199. Proc Natl Acad Sci U S A. 1979. PMID: 375229 Free PMC article.
-
Minor coat protein composition and location of the A protein in bacteriophage f1 spheroids and I-forms.J Virol. 1982 Jun;42(3):1099-107. doi: 10.1128/JVI.42.3.1099-1107.1982. J Virol. 1982. PMID: 7097858 Free PMC article.
-
Chemical modification of the coat protein in bacteriophage fd and orientation of the virion during assembly and disassembly.EMBO J. 1983;2(10):1641-6. doi: 10.1002/j.1460-2075.1983.tb01638.x. EMBO J. 1983. PMID: 6357778 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources