Novel insight into an energy transduction mechanism of the bacterial flagellar type III protein export

被引:3
|
作者
Terashima, Hiroyuki [1 ]
Imada, Katsumi [2 ]
机构
[1] Nagoya Univ, Grad Sch Sci, Div Biol Sci, Nagoya, Aichi 4648602, Japan
[2] Osaka Univ, Grad Sch Sci, Toyonaka, Osaka 5600043, Japan
来源
关键词
In vitro reconstitution; Inverted membrane vesicle; Type III secretion system; injectisome; bacterial flagellum;
D O I
10.2142/biophysico.15.0_173
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Type III secretion system (T3SS) is a protein translocator complex family including pathogenic injectisome or bacterial flagellum. The inejectisomal T3SS serves to deliver virulence proteins into host cell and the flagellar T3SS constructs the flagellar axial structure. Although earlier studies have provided many findings on the molecular mechanism of the Type III protein export, they were not sufficient to reveal energy transduction mechanism due to difficulties in controlling measurement conditions in vivo. Recently, we developed an in vitro flagellar Type III protein transport assay system using inverted membrane vesicles (IMVs), and analyzed protein export by using the in vitro method. We reproduced protein export of the flagellar T3SS, hook assembly and substrate specificity switch in IMV to a similar extent to what is seen in living cell. Furthermore, we demonstrated that ATP-hydrolysis energy can drive protein transport even in the absence of proton-motive force (PMF). In this mini-review, we will summarize our new in vitro Type III transport assay method and our findings on the molecular mechanism of Type III protein export.
引用
收藏
页码:173 / 178
页数:6
相关论文
共 50 条
  • [1] An energy transduction mechanism used in bacterial flagellar type III protein export
    Minamino, Tohru
    Morimoto, Yusuke V.
    Hara, Noritaka
    Namba, Keiichi
    NATURE COMMUNICATIONS, 2011, 2
  • [2] An energy transduction mechanism used in bacterial flagellar type III protein export
    Tohru Minamino
    Yusuke V. Morimoto
    Noritaka Hara
    Keiichi Namba
    Nature Communications, 2
  • [4] Protein export through the bacterial flagellar type III export pathway
    Minamino, Tohru
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2014, 1843 (08): : 1642 - 1648
  • [5] Insight into structural remodeling of the FlhA ring responsible for bacterial flagellar type III protein export
    Terahara, Naoya
    Inoue, Yumi
    Kodera, Noriyuki
    Morimoto, Yusuke V.
    Uchihashi, Takayuki
    Imada, Katsumi
    Ando, Toshio
    Namba, Keiichi
    Minamino, Tohru
    SCIENCE ADVANCES, 2018, 4 (04):
  • [6] Type III flagellar protein export and flagellar assembly
    Macnab, RM
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2004, 1694 (1-3): : 207 - 217
  • [7] Genetic Characterization of Conserved Charged Residues in the Bacterial Flagellar Type III Export Protein FlhA
    Hara, Noritaka
    Namba, Keiichi
    Minamino, Tohru
    PLOS ONE, 2011, 6 (07):
  • [8] Biophysical Mechanism of Protein Export by Bacterial Type III Secretion System
    Ohgita, Takashi
    Saito, Hiroyuki
    CHEMICAL & PHARMACEUTICAL BULLETIN, 2019, 67 (04) : 341 - 344
  • [9] Role of the C-Terminal Cytoplasmic Domain of FlhA in Bacterial Flagellar Type III Protein Export
    Minamino, Tohru
    Shimada, Masafumi
    Okabe, Mayuko
    Saijo-Hamano, Yumiko
    Imada, Katsumi
    Kihara, May
    Namba, Keiichi
    JOURNAL OF BACTERIOLOGY, 2010, 192 (07) : 1929 - 1936
  • [10] FliH and FliI ensure efficient energy coupling of flagellar type III protein export in Salmonella
    Minamino, Tohru
    Kinoshita, Miki
    Inoue, Yumi
    Morimoto, Yusuke V.
    Ihara, Kunio
    Koya, Satomi
    Hara, Noritaka
    Nishioka, Noriko
    Kojima, Seiji
    Homma, Michio
    Namba, Keiichi
    MICROBIOLOGYOPEN, 2016, 5 (03): : 424 - 435