Home LiteratureArticle Details
PMID: 11684686 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The elastin-binding protein of Staphylococcus aureus (EbpS) is expressed at the cell surface as an integral membrane protein and not as a cell wall-associated protein.

The Journal of biological chemistry ·Vol. 277 ·No. 1 ·2002-01-04 ·Pages 243-50

Downer R, Roche F, Park PW, Mecham RP, Foster TJ

Abstract

The elastin-binding proteins EbpS of Staphylococcus aureus strains Cowan and 8325-4 were predicted from sequence analysis to comprise 486 residues. Specific antibodies were raised against an N-terminal domain (residues 1-267) and a C-terminal domain (residues 343-486) expressed as recombinant proteins in Escherichia coli. Western blotting of lysates of wild-type 8325-4 and Newman and the corresponding ebpS mutants showed that EbpS migrated with an apparent molecular mass of 83 kDa. The protein was found exclusively in cytoplasmic membrane fractions purified from protoplasts or lysed cells, in contrast to the clumping factor ClfA, which was cell-wall-associated. EbpS was predicted to have three hydrophobic domains H1-(205-224), H2-(265-280), and H3-(315-342). A series of hybrid proteins was formed between EbpS at the N terminus and either alkaline phosphatase or beta-galactosidase at the C terminus (EbpS-PhoA, EbpS-LacZ). PhoA and LacZ were fused to EbpS between hydrophobic domains H1-H2 and H2-H3, and distal to H3. Expression of enzymatic activity in E. coli showed that EbpS is an integral membrane protein with two membrane-spanning domains H1 and H3. N-terminal residues 1-205 and C-terminal residues 343-486 were predicted to be exposed on the outer face of the cytoplasmic membrane. The ligand-binding domain of EbpS is known from previous studies to be present in the N terminus between residues 14-34 and probing whole cells with anti-EbpS1-267 antibodies indicated that this region is exposed on the surface of intact cells. This was also confirmed by the observation that wild-type S. aureus Newman cells bound labeled tropoelastin whereas the ebpS mutant bound 72% less. In contrast, the C terminus, which carries a putative LysM peptidoglycan-binding domain, is not exposed on the surface of intact cells and presumably remains buried within the peptidoglycan. Finally, expression of EbpS was correlated with the ability of cells to grow to a higher density in liquid culture, suggesting that EbpS may have a role in regulating cell growth.

MeSH Terms
Animals Bacterial Proteins/analysis Base Sequence Blotting, Western Cell Wall/chemistry Cytoplasm/chemistry Elastin/metabolism Membrane Proteins/analysis Molecular Sequence Data Rabbits Receptors, Cell Surface/analysis,genetics,metabolism Recombinant Fusion Proteins/analysis Staphylococcus aureus/chemistry Tropoelastin/metabolism
Chemicals
Bacterial Proteins Membrane Proteins Receptors, Cell Surface Recombinant Fusion Proteins Tropoelastin elastin-binding proteins Elastin
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Downer Robert
Microbiology Department, Moyne Institute of Preventive Medicine, Trinity College, Dublin 2, Ireland.
Roche Fiona
Park Pyong Woo
Mecham Robert P
Foster Timothy J
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2002-01-04
Epub
2001-00-29
Pages
243-50
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Databases
GENBANK
AF400161, U48826
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com