Peter J. Christie, Ph.D.
Department of Microbiology &
University of Texas-Houston Medical School
6431 Fannin Street, MSB 1.164
Houston, Texas 77030
Telephone: (713) 500-5440
Laboratory Telephone: (713) 500-7441
Ph.D., Cornell University, 1986
Postdoctoral Fellow, University of Washington & Stanford University
Macromolecular transport processes during pathogenesis
Translocation of macromolecules between cells is a major area of biomedical interest. The focus of study in this laboratory is a type IV secretion (T4S) system of Agrobacterium tumefaciens. This system is ancestrally related and functionally similar to bacterial conjugation systems, as well as recently described protein translocation systems used by bacterial pathogens during the course of infection This T4S system mediates transfer of diverse substrates including oncogenic DNA and other DNA in the form of nucleoprotein particles, and of protein monomers across the A. tumefaciens cell envelope. These substrates are delivered to a variety of phylogenetically-diverse target bacterial or eukaryotic cells through a process dependent on direct cell-to-cell contact. This T4S system, assembled from VirD4 and 11 VirB subunits, is an especially attractive system for detailed mechanistic studies of macromolecular transport because of the ease of manipulation of A. tumefaciens, the large numbers of strains, constructs, and other molecular tools at hand, and the wealth of information about it and closely related transfer systems. We also are developing studies of other T4S systems of Gram-negative and Gram-positive bacterial pathogens.
The overall goal of work in this laboratory is to describe in detailed mechanistic terms the dynamic processes required for biogenesis and function of T4S systems during infection. We use powerful in vivo technologies developed in this laboratory and other state-of-the art biochemical and structure-based approaches to define how DNA and protein substrates are recruited to and translocated through the T4S channels.
Questions of particular interest at this time include:
- How do three ATPase subunits energize machine assembly or function?
- How are substrates recruited to the secretion channel?
- What is the route of substrate transfer through the secretory apparatus?
- How do bacterial cells establish contact with bacterial or eukaryotic target cells to mediate intercellular substrate transfer?
- What are the cellular consequences of substrate trafficking in the host cell?
- Cascales and Christie 2003
- Jakubowski et al. 2005
Supplemental material for P.J. Christie, K. Atmakuri, V. Krishnamoorthy, S. Jakubowski,and E. Cascales. (2005) Biogenesis, Architecture, and Function of Bacterial Type IV Secretion Systems. Annu. Rev. Microbiol. 59:451-485.
- Download all alignments (3.1 MB file, 86 pages)
- Download alignment VirB1
- Download alignment VirB2
- Download alignment VirB3
- Download alignment VirB4
- Download alignment VirB5
- Download alignment VirB6
- Download alignment VirB7
- Download alignment VirB8
- Download alignment VirB9
- Download alignment VirB10
- Download alignment VirB11
- Download alignment VirD4
- Berry, T.M., Christie PJ. (2011) Caught in the act: The dialogue between bacteriophage R17 and the type IV secretion machine of plasmid R1. Mol. Microbiol. 82:1039-1043. [abstract]
- Banta, L.M., Kerr, J.E., Cascales, E., Giuliano, M.E., Bailey, M.E., McKay, C., Chandran, V., Waksman, G., Christie PJ. (2011) An Agrobacterium VirB10 mutation conferring a type IV secretion system gating defect. J. Bacteriol. 193:2566-2574. [abstract]
- Kerr, J.E., Christie PJ. (2010) Evidence for VirB4-mediated dislocation of membrane-integrated VirB2 pilin during biogenesis of the Agrobacterium VirB/VirD4 type IV secretion system. J. Bacteriol. 192:4923-4934. [abstract]
- Christie PJ. (2009) Structural biology: Translocation chamber's secrets. Nature. 462:992-994. No abstract available.
- Alvarez-Martinez, C.E., Christie PJ. (2009) Biological diversity of prokaryotic type IV secretion systems. Microbiol. Mol. Biol. Rev. 73:775-808. [abstract]
- Fronzes, R., Christie PJ, Waksman, G. (2009) The structural biology of type IV secretion systems. Nat. Rev. Microbiol. 7:703-714. [abstract]
- Jakubowski, S.J., Kerr, J.E., Garza, I., Krishnamoorthy, V., Bayliss, R., Waksman, G., Christie PJ. (2009) Agrobacterium VirB10 domain requirements for type IV secretion and T pilus biogenesis. Mol. Microbiol. 71:779-794. [abstract]
- Chen, Y., Zhang, X., Manias, D., Yeo, H.J., Dunny, G.M., Christie PJ. (2008) Enterococcus faecalis PcfC, a spatially localized substrate receptor for type IV secretion of the pCF10 transfer intermediate. J. Bacteriol. 190:3632-3645. [abstract]
- Atmakuri, K., Cascales, E., Burton, O.T., Banta, L.M., Christie PJ. (2007) Agrobacterium ParA/MinD-like VirC1 spatially coordinates early conjugative DNA transfer reactions. EMBO J. 26:2540-2551. [abstract]
- Bayliss, R., Harris, R., Coutte, L., Monier, A., Christie PJ, Driscoll, P.C., Waksman, G. (2007) NMR structure of a complex between the VirB9/BirB7 interaction domains of the pKM101 type IV secretion system. Proc. Natl. Acad. Sci. 104:1673-1678. [abstract]
- [Search PubMed for more papers by Peter J. Christie]
Location & Contact
6431 Fannin Street,
Houston, Texas 77030
P.O. Box 20708
Houston, Texas 77225
Our affiliates include the following:
- Departmental Faculty
- Theresa M. Koehler, Ph.D.
- Peter J. Christie, Ph.D.
- Nicholas De Lay, Ph.D.
- Jesus Eraso, Ph.D.
- Danielle Garsin, Ph.D.
- Heidi Kaplan, Ph.D.
- Samuel Kaplan, Ph.D.
- Nayun Kim, Ph.D.
- Ziyin Li, Ph.D.
- Jiqiang (Lanny) Ling, Ph.D.
- Michael C. Lorenz, Ph.D.
- Chris Mackenzie, Ph.D.
- William Margolin, Ph.D.
- Kevin A. Morano, Ph.D.
- Hung Ton-That, Ph.D.
- Ambro van Hoof, Ph.D.
- Departmental Faculty - Cross Appointees
- William Dowhan, Ph.D.
- Millicent Goldschmidt, Ph.D.
- Barrett Harvey, Ph.D.
- Jun Liu, Ph.D.
- Barbara E. Murray, M.D.
- Steven J. Norris, Ph.D.
- John L. Spudich, Ph.D.
- Adjunct Faculty
- Magnus Höök, Ph.D.
- Gregory S. May, Ph.D.
- Yi Xu, Ph.D.