Literature DB >> 16343541

Unassisted membrane insertion as the initial step in DeltapH/Tat-dependent protein transport.

Bo Hou1, Stefan Frielingsdorf, Ralf Bernd Klösgen.   

Abstract

In the thylakoid membrane of chloroplasts as well as in the cytoplasmic membrane of bacteria, the DeltapH/Tat-dependent protein transport pathway is responsible for the translocation of folded proteins. Using the chimeric 16/23 protein as model substrate in thylakoid transport experiments, we dissected the transport process into several distinct steps that are characterized by specific integral translocation intermediates. Formation of the early translocation intermediate Ti-1, which still exposes the N and the C terminus to the stroma, is observed with thylakoids pretreated with (i) solutions of chaotropic salts or alkaline pH, (ii) protease, or (iii) antibodies raised against TatA, TatB, or TatC. Membrane insertion takes place even into liposomes, demonstrating that proteinaceous components are not required. This suggests that Tat-dependent transport may be initiated by the unassisted insertion of the substrate into the lipid bilayer, and that interaction with the Tat translocase takes place only in later stages of the process.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16343541     DOI: 10.1016/j.jmb.2005.11.029

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  22 in total

1.  Mapping precursor-binding site on TatC subunit of twin arginine-specific protein translocase by site-specific photo cross-linking.

Authors:  Stefan Zoufaly; Julia Fröbel; Patrick Rose; Tobias Flecken; Carlo Maurer; Michael Moser; Matthias Müller
Journal:  J Biol Chem       Date:  2012-02-23       Impact factor: 5.157

Review 2.  Twin-arginine-dependent translocation of folded proteins.

Authors:  Julia Fröbel; Patrick Rose; Matthias Müller
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2012-04-19       Impact factor: 6.237

3.  Multiple precursor proteins bind individual Tat receptor complexes and are collectively transported.

Authors:  Xianyue Ma; Kenneth Cline
Journal:  EMBO J       Date:  2010-03-25       Impact factor: 11.598

4.  Kinetics of precursor interactions with the bacterial Tat translocase detected by real-time FRET.

Authors:  Neal Whitaker; Umesh K Bageshwar; Siegfried M Musser
Journal:  J Biol Chem       Date:  2012-02-07       Impact factor: 5.157

5.  A stromal pool of TatA promotes Tat-dependent protein transport across the thylakoid membrane.

Authors:  Stefan Frielingsdorf; Mario Jakob; Ralf Bernd Klösgen
Journal:  J Biol Chem       Date:  2008-10-07       Impact factor: 5.157

Review 6.  Mechanistic Aspects of Folded Protein Transport by the Twin Arginine Translocase (Tat).

Authors:  Kenneth Cline
Journal:  J Biol Chem       Date:  2015-05-14       Impact factor: 5.157

Review 7.  Routing of thylakoid lumen proteins by the chloroplast twin arginine transport pathway.

Authors:  Christopher Paul New; Qianqian Ma; Carole Dabney-Smith
Journal:  Photosynth Res       Date:  2018-08-12       Impact factor: 3.573

8.  A Hinged Signal Peptide Hairpin Enables Tat-Dependent Protein Translocation.

Authors:  Shruthi Hamsanathan; Tamil S Anthonymuthu; Umesh K Bageshwar; Siegfried M Musser
Journal:  Biophys J       Date:  2017-12-19       Impact factor: 4.033

9.  The h-region of twin-arginine signal peptides supports productive binding of bacterial Tat precursor proteins to the TatBC receptor complex.

Authors:  Agnes Ulfig; Julia Fröbel; Frank Lausberg; Anne-Sophie Blümmel; Anna Katharina Heide; Matthias Müller; Roland Freudl
Journal:  J Biol Chem       Date:  2017-05-17       Impact factor: 5.157

10.  TatB functions as an oligomeric binding site for folded Tat precursor proteins.

Authors:  Carlo Maurer; Sascha Panahandeh; Anna-Carina Jungkamp; Michael Moser; Matthias Müller
Journal:  Mol Biol Cell       Date:  2010-10-06       Impact factor: 4.138

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.