This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Harris, C. R.
Right arrow Articles by Silhavy, T. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Harris, C. R.
Right arrow Articles by Silhavy, T. J.

 Previous Article  |  Next Article 

Journal of Bacteriology, June 1999, p. 3438-3444, Vol. 181, No. 11
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Mapping an Interface of SecY (PrlA) and SecE (PrlG) by Using Synthetic Phenotypes and In Vivo Cross-Linking

Chris R. Harris and Thomas J. Silhavy*

Department of Molecular Biology, Princeton University, Princeton, New Jersey 08544

Received 15 January 1999/Accepted 6 April 1999

SecY and SecE are integral cytoplasmic membrane proteins that form an essential part of the protein translocation machinery in Escherichia coli. Sites of direct contact between these two proteins have been suggested by the allele-specific synthetic phenotypes exhibited by pairwise combinations of prlA and prlG signal sequence suppressor mutations in these genes. We have introduced cysteine residues within the first periplasmic loop of SecY and the second periplasmic loop of SecE, at a specific pair of positions identified by this genetic interaction. The expression of the cysteine mutant pair results in a dominant lethal phenotype that requires the presence of DsbA, which catalyzes the formation of disulfide bonds. A reducible SecY-SecE complex is also observed, demonstrating that these amino acids must be sufficiently proximal to form a disulfide bond. The use of cysteine-scanning mutagenesis enabled a second contact site to be discovered. Together, these two points of contact allow the modeling of a limited region of quaternary structure, establishing the first characterized site of interaction between these two proteins. This study proves that actual points of protein-protein contact can be identified by using synthetic phenotypes.


* Corresponding author. Mailing address: Princeton University, Department of Molecular Biology, 310 Lewis Thomas Laboratory, Washington Rd., Princeton, NJ 08544. Phone: (617) 258-5899. Fax: (617) 258-2957. E-mail: tsilhavy{at}molbio.princeton.edu.


Journal of Bacteriology, June 1999, p. 3438-3444, Vol. 181, No. 11
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Boy, D., Koch, H.-G. (2009). Visualization of Distinct Entities of the SecYEG Translocon during Translocation and Integration of Bacterial Proteins. Mol. Biol. Cell 20: 1804-1815 [Abstract] [Full Text]  
  • Gumbart, J., Schulten, K. (2008). The Roles of Pore Ring and Plug in the SecY Protein-conducting Channel. JGP 132: 709-719 [Abstract] [Full Text]  
  • Erlandson, K. J., Or, E., Osborne, A. R., Rapoport, T. A. (2008). Analysis of Polypeptide Movement in the SecY Channel during SecA-mediated Protein Translocation. J. Biol. Chem. 283: 15709-15715 [Abstract] [Full Text]  
  • Bol, R., de Wit, J. G., Driessen, A. J. M. (2007). The Active Protein-conducting Channel of Escherichia coli Contains an Apolar Patch. J. Biol. Chem. 282: 29785-29793 [Abstract] [Full Text]  
  • Maillard, A. P., Lalani, S., Silva, F., Belin, D., Duong, F. (2007). Deregulation of the SecYEG Translocation Channel upon Removal of the Plug Domain. J. Biol. Chem. 282: 1281-1287 [Abstract] [Full Text]  
  • Barak, Y., Ackerley, D. F., Dodge, C. J., Banwari, L., Alex, C., Francis, A. J., Matin, A. (2006). Analysis of novel soluble chromate and uranyl reductases and generation of an improved enzyme by directed evolution.. Appl. Environ. Microbiol. 72: 7074-7082 [Abstract] [Full Text]  
  • Junne, T., Schwede, T., Goder, V., Spiess, M. (2006). The Plug Domain of Yeast Sec61p Is Important for Efficient Protein Translocation, but Is Not Essential for Cell Viability. Mol. Biol. Cell 17: 4063-4068 [Abstract] [Full Text]  
  • Smith, M. A., Clemons, W. M. Jr., DeMars, C. J., Flower, A. M. (2005). Modeling the Effects of prl Mutations on the Escherichia coli SecY Complex. J. Bacteriol. 187: 6454-6465 [Abstract] [Full Text]  
  • Cannon, K. S., Or, E., Clemons, W. M. Jr., Shibata, Y., Rapoport, T. A. (2005). Disulfide bridge formation between SecY and a translocating polypeptide localizes the translocation pore to the center of SecY. JCB 169: 219-225 [Abstract] [Full Text]  
  • Veenendaal, A. K. J., van der Does, C., Driessen, A. J. M. (2002). The Core of the Bacterial Translocase Harbors a Tilted Transmembrane Segment 3 of SecE. J. Biol. Chem. 277: 36640-36645 [Abstract] [Full Text]  
  • Rizzitello, A. E., Harper, J. R., Silhavy, T. J. (2001). Genetic Evidence for Parallel Pathways of Chaperone Activity in the Periplasm of Escherichia coli. J. Bacteriol. 183: 6794-6800 [Abstract] [Full Text]  
  • Swaving, J., van Wely, K. H. M., Driessen, A. J. M. (1999). Preprotein Translocation by a Hybrid Translocase Composed of Escherichia coli and Bacillus subtilis Subunits. J. Bacteriol. 181: 7021-7027 [Abstract] [Full Text]  
  • Dapic, V., Oliver, D. (2000). Distinct Membrane Binding Properties of N- and C-terminal Domains of Escherichia coli SecA ATPase. J. Biol. Chem. 275: 25000-25007 [Abstract] [Full Text]  
  • Veenendaal, A. K. J., van der Does, C., Driessen, A. J. M. (2001). Mapping the Sites of Interaction between SecY and SecE by Cysteine Scanning Mutagenesis. J. Biol. Chem. 276: 32559-32566 [Abstract] [Full Text]