Catch and arrest: exploiting the retromer by a Chlamydial effector

被引:4
|
作者
Luo, Zhao-Qing [1 ,2 ]
机构
[1] Purdue Univ, Purdue Inst Inflammat Immunol & Infect Dis, W Lafayette, IN 47907 USA
[2] Purdue Univ, Dept Biol Sci, W Lafayette, IN 47907 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/sigtrans.2017.39
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The pathogen behind chlamydia releases a protein called IncE that interacts with a particular host protein to disrupt cell trafficking. In a commentary article, Zhao-Qing Luo from Purdue University in West Lafayette, Indiana, USA, discusses three recent structural studies that independently explored how the Chlamydia bacterium creates a privileged home in the cell ? a membrane-bound compartment termed inclusion ? from which it secretes IncE and other so-called inclusion membrane proteins to manipulate host processes for its own survival. These studies identified a small region of IncE that recognizes with high affinity the SNX5 protein, a component of the retromer complex involved in recycling the cell?s secretory machinery. These structural insights could help researchers combat chlamydial infections, a major cause of sexually transmitted and ocular diseases for which no vaccines exist.
引用
收藏
页数:2
相关论文
共 50 条
  • [41] Solution structure and biophysical characterization of the multifaceted signalling effector protein growth arrest specific-1
    Rosti, Katja
    Goldman, Adrian
    Kajander, Tommi
    BMC BIOCHEMISTRY, 2015, 16
  • [42] Simplified Evaluation Method for Brittle Crack Arrest Toughness of Steel Plates Exploiting Charpy Impact Test
    Shirahata, Hiroyuki
    Okawa, Teppei
    Inoue, Takehiro
    Ushioda, Kohsaku
    TETSU TO HAGANE-JOURNAL OF THE IRON AND STEEL INSTITUTE OF JAPAN, 2018, 104 (03): : 155 - 165
  • [43] A bacterial type III effector family uses the papain-like hydrolytic activity to arrest the host cell cycle
    Yao, Qing
    Cui, Jixin
    Zhu, Yongqun
    Wang, Guolun
    Hu, Liyan
    Long, Chengzu
    Cao, Ran
    Liu, Xinqi
    Huang, Niu
    Chen, She
    Liu, Liping
    Shao, Feng
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (10) : 3716 - 3721
  • [44] Magic and the Brain Magicians have been testing and exploiting the limits of cognition and attention for hundreds of years. Neuroscientists are just beginning to catch up
    Martinez-Conde, Susana
    Macknik, Stephen L.
    SCIENTIFIC AMERICAN, 2008, 299 (06) : 72 - 79
  • [45] Angler Behaviors and Motivations for Exploiting Invasive and Native Predatory Fishes by Catch-and-Release: A Case Study on the River Severn Catchment, Western England
    Nolan, Emma T.
    Britton, J. Robert
    Curtin, Susanna
    HUMAN DIMENSIONS OF WILDLIFE, 2019, 24 (05) : 463 - 479
  • [46] Cell cycle arrest caused by MEK/ERK signaling is a mechanism for suppressing growth of antigen-hyperstimulated effector T cells
    Ohtsuka, Shizuka
    Ogawa, Shuhei
    Wakamatsu, Ei
    Abe, Ryo
    INTERNATIONAL IMMUNOLOGY, 2016, 28 (11) : 547 - 557
  • [47] Cell-nonautonomous local and systemic responses to cell arrest enable long-bone catch-up growth in developing mice
    Rosello-Diez, Alberto
    Madisen, Linda
    Bastide, Sebastien
    Zeng, Hongkui
    Joyner, Alexandra L.
    PLOS BIOLOGY, 2018, 16 (06)
  • [48] Traditional management strategies fail to arrest a decline in the catch-per-unit-effort of an iconic marine recreational fishery species with evidence of hyperstability
    Maggs, J. Q.
    Mann, B. Q.
    Potts, W. M.
    Dunlop, S. W.
    FISHERIES MANAGEMENT AND ECOLOGY, 2016, 23 (3-4) : 187 - 199
  • [49] P15(INK4B) IS A POTENTIAL EFFECTOR OF TGF-BETA-INDUCED CELL-CYCLE ARREST
    HANNON, GJ
    BEACH, D
    NATURE, 1994, 371 (6494) : 257 - 261
  • [50] Expression of the Bacterial Type III Effector DspA/E in Saccharomyces cerevisiae Down-regulates the Sphingolipid Biosynthetic Pathway Leading to Growth Arrest
    Siamer, Sabrina
    Guillas, Isabelle
    Shimobayashi, Mitsugu
    Kunz, Caroline
    Hall, Michael N.
    Barny, Marie-Anne
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2014, 289 (26) : 18466 - 18477