Literature DB >> 21460239

Synergistic actions between the SRP RNA and translating ribosome allow efficient delivery of the correct cargos during cotranslational protein targeting.

Kuang Shen1, Xin Zhang, Shu-Ou Shan.   

Abstract

During cotranslational protein targeting by the Signal Recognition Particle (SRP), the correct cargo accelerates stable complex assembly between the SRP and SRP receptor (FtsY) by several orders of magnitude, thus enabling rapid and faithful cargo delivery to the target membrane. The molecular mechanism underlying this cargo-induced rate acceleration has been unclear. Here we show that the SRP RNA allows assembly of the SRP-FtsY complex to be specifically stimulated by a correct cargo, and, reciprocally, a correct cargo enables the SRP RNA to optimize its electrostatic interactions with FtsY. These results combined with recent structural work led us to suggest a "conformational selection" model that explains the synergistic action of the SRP RNA with the cargo in accelerating complex assembly. In addition to its previously proposed role in preventing the premature dissociation of SRP and FtsY, we found that the SRP RNA also plays an active role in ensuring the formation of productive assembly intermediates, thus guiding the SRP and FtsY through the most efficient pathway of assembly.

Mesh:

Substances:

Year:  2011        PMID: 21460239      PMCID: PMC3078738          DOI: 10.1261/rna.2610411

Source DB:  PubMed          Journal:  RNA        ISSN: 1355-8382            Impact factor:   4.942


  36 in total

1.  Crystal structure of the ribonucleoprotein core of the signal recognition particle.

Authors:  R T Batey; R P Rambo; L Lucast; B Rha; J A Doudna
Journal:  Science       Date:  2000-02-18       Impact factor: 47.728

2.  Role of SRP RNA in the GTPase cycles of Ffh and FtsY.

Authors:  P Peluso; S O Shan; S Nock; D Herschlag; P Walter
Journal:  Biochemistry       Date:  2001-12-18       Impact factor: 3.162

3.  Signal recognition particle binds to ribosome-bound signal sequences with fluorescence-detected subnanomolar affinity that does not diminish as the nascent chain lengthens.

Authors:  John J Flanagan; Jui-Chang Chen; Yiwei Miao; Yuanlong Shao; Jialing Lin; Paul E Bock; Arthur E Johnson
Journal:  J Biol Chem       Date:  2003-03-05       Impact factor: 5.157

4.  Crystal structure of the complete core of archaeal signal recognition particle and implications for interdomain communication.

Authors:  Ken R Rosendal; Klemens Wild; Guillermo Montoya; Irmgard Sinning
Journal:  Proc Natl Acad Sci U S A       Date:  2003-12-01       Impact factor: 11.205

5.  Distinct modes of signal recognition particle interaction with the ribosome.

Authors:  Martin R Pool; Joachim Stumm; Tudor A Fulga; Irmgard Sinning; Bernhard Dobberstein
Journal:  Science       Date:  2002-08-23       Impact factor: 47.728

6.  Substrate twinning activates the signal recognition particle and its receptor.

Authors:  Pascal F Egea; Shu-Ou Shan; Johanna Napetschnig; David F Savage; Peter Walter; Robert M Stroud
Journal:  Nature       Date:  2004-01-15       Impact factor: 49.962

7.  Heterodimeric GTPase core of the SRP targeting complex.

Authors:  Pamela J Focia; Irina V Shepotinovskaya; James A Seidler; Douglas M Freymann
Journal:  Science       Date:  2004-01-16       Impact factor: 47.728

8.  Structure of the signal recognition particle interacting with the elongation-arrested ribosome.

Authors:  Mario Halic; Thomas Becker; Martin R Pool; Christian M T Spahn; Robert A Grassucci; Joachim Frank; Roland Beckmann
Journal:  Nature       Date:  2004-02-26       Impact factor: 49.962

9.  The signal recognition particle binds to protein L23 at the peptide exit of the Escherichia coli ribosome.

Authors:  Shan-Qing Gu; Frank Peske; Hans-Joachim Wieden; Marina V Rodnina; Wolfgang Wintermeyer
Journal:  RNA       Date:  2003-05       Impact factor: 4.942

10.  Interplay of signal recognition particle and trigger factor at L23 near the nascent chain exit site on the Escherichia coli ribosome.

Authors:  Ronald S Ullers; Edith N G Houben; Amanda Raine; Corinne M ten Hagen-Jongman; Måns Ehrenberg; Joseph Brunner; Bauke Oudega; Nellie Harms; Joen Luirink
Journal:  J Cell Biol       Date:  2003-05-19       Impact factor: 10.539

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  20 in total

1.  Translation elongation regulates substrate selection by the signal recognition particle.

Authors:  Dawei Zhang; Shu-ou Shan
Journal:  J Biol Chem       Date:  2012-01-06       Impact factor: 5.157

2.  Translational arrest by a prokaryotic signal recognition particle is mediated by RNA interactions.

Authors:  Bertrand Beckert; Alexej Kedrov; Daniel Sohmen; Georg Kempf; Klemens Wild; Irmgard Sinning; Henning Stahlberg; Daniel N Wilson; Roland Beckmann
Journal:  Nat Struct Mol Biol       Date:  2015-09-07       Impact factor: 15.369

3.  Molecular mechanism of GTPase activation at the signal recognition particle (SRP) RNA distal end.

Authors:  Kuang Shen; Yaqiang Wang; Yu-Hsien Hwang Fu; Qi Zhang; Juli Feigon; Shu-ou Shan
Journal:  J Biol Chem       Date:  2013-10-22       Impact factor: 5.157

Review 4.  A tale of two GTPases in cotranslational protein targeting.

Authors:  Ishu Saraogi; David Akopian; Shu-Ou Shan
Journal:  Protein Sci       Date:  2011-09-27       Impact factor: 6.725

5.  Co-evolution of Two GTPases Enables Efficient Protein Targeting in an RNA-less Chloroplast Signal Recognition Particle Pathway.

Authors:  Sowmya Chandrasekar; Michael J Sweredoski; Chang Ho Sohn; Sonja Hess; Shu-Ou Shan
Journal:  J Biol Chem       Date:  2016-11-28       Impact factor: 5.157

6.  Sequential activation of human signal recognition particle by the ribosome and signal sequence drives efficient protein targeting.

Authors:  Jae Ho Lee; Sowmya Chandrasekar; SangYoon Chung; Yu-Hsien Hwang Fu; Demi Liu; Shimon Weiss; Shu-Ou Shan
Journal:  Proc Natl Acad Sci U S A       Date:  2018-05-30       Impact factor: 11.205

7.  Dynamic switch of the signal recognition particle from scanning to targeting.

Authors:  Wolf Holtkamp; Sejeong Lee; Thomas Bornemann; Tamara Senyushkina; Marina V Rodnina; Wolfgang Wintermeyer
Journal:  Nat Struct Mol Biol       Date:  2012-11-11       Impact factor: 15.369

8.  Allosteric response and substrate sensitivity in peptide binding of the signal recognition particle.

Authors:  Connie Y Wang; Thomas F Miller
Journal:  J Biol Chem       Date:  2014-09-18       Impact factor: 5.157

9.  Anionic Phospholipids and the Albino3 Translocase Activate Signal Recognition Particle-Receptor Interaction during Light-harvesting Chlorophyll a/b-binding Protein Targeting.

Authors:  Sowmya Chandrasekar; Shu-Ou Shan
Journal:  J Biol Chem       Date:  2016-11-28       Impact factor: 5.157

Review 10.  ATPase and GTPase Tangos Drive Intracellular Protein Transport.

Authors:  Shu-Ou Shan
Journal:  Trends Biochem Sci       Date:  2016-09-19       Impact factor: 13.807

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