Erin D Goley

Summary

Affiliation: Stanford University
Country: USA

Publications

  1. pmc Imaging-based identification of a critical regulator of FtsZ protofilament curvature in Caulobacter
    Erin D Goley
    Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA
    Mol Cell 39:975-87. 2010
  2. pmc Assembly of the Caulobacter cell division machine
    Erin D Goley
    Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA
    Mol Microbiol 80:1680-98. 2011
  3. pmc DipM links peptidoglycan remodelling to outer membrane organization in Caulobacter
    Erin D Goley
    Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA
    Mol Microbiol 77:56-73. 2010
  4. pmc Three-dimensional super-resolution imaging of the midplane protein FtsZ in live Caulobacter crescentus cells using astigmatism
    Julie S Biteen
    Department of Chemistry, Stanford University, Stanford, CA 94305, USA
    Chemphyschem 13:1007-12. 2012
  5. ncbi Cell cycle regulation in Caulobacter: location, location, location
    Erin D Goley
    Department of Developmental Biology, Beckman Center, Stanford University School of Medicine, 279 Campus Drive, Stanford, CA 94305, USA
    J Cell Sci 120:3501-7. 2007
  6. pmc Superresolution imaging of targeted proteins in fixed and living cells using photoactivatable organic fluorophores
    Hsiao lu D Lee
    Department of Chemistry, Stanford University, Stanford, California 94305, USA
    J Am Chem Soc 132:15099-101. 2010

Collaborators

Detail Information

Publications6

  1. pmc Imaging-based identification of a critical regulator of FtsZ protofilament curvature in Caulobacter
    Erin D Goley
    Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA
    Mol Cell 39:975-87. 2010
    ..The degree of curvature induced by FzlA depended on the nucleotide bound to FtsZ. Induction of FtsZ curvature by FzlA carries implications for regulating FtsZ function by modulating its superstructure...
  2. pmc Assembly of the Caulobacter cell division machine
    Erin D Goley
    Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA
    Mol Microbiol 80:1680-98. 2011
    ..Our analysis revealed differences in divisome assembly among Caulobacter and other bacteria that establish a framework for identifying aspects of bacterial cytokinesis that are widely conserved from those that are more variable...
  3. pmc DipM links peptidoglycan remodelling to outer membrane organization in Caulobacter
    Erin D Goley
    Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA
    Mol Microbiol 77:56-73. 2010
    ..We conclude that DipM is required for normal envelope invagination during division and to maintain a sacculus of constant thickness that allows for maintenance of OM connections throughout the cell envelope...
  4. pmc Three-dimensional super-resolution imaging of the midplane protein FtsZ in live Caulobacter crescentus cells using astigmatism
    Julie S Biteen
    Department of Chemistry, Stanford University, Stanford, CA 94305, USA
    Chemphyschem 13:1007-12. 2012
    ..crescentus cells at different stages of the cell cycle and find that the FtsZ superstructure is dynamic with the cell cycle, forming an open shape during the stalked stage and a dense focus during the pre-divisional stage...
  5. ncbi Cell cycle regulation in Caulobacter: location, location, location
    Erin D Goley
    Department of Developmental Biology, Beckman Center, Stanford University School of Medicine, 279 Campus Drive, Stanford, CA 94305, USA
    J Cell Sci 120:3501-7. 2007
    ....
  6. pmc Superresolution imaging of targeted proteins in fixed and living cells using photoactivatable organic fluorophores
    Hsiao lu D Lee
    Department of Chemistry, Stanford University, Stanford, California 94305, USA
    J Am Chem Soc 132:15099-101. 2010
    ....