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Targeting of proteins to appropriate subcellular compartments is a crucial process in all living cells. Secretory and membrane proteins usually contain an amino-terminal signal peptide, which is recognized by the signal recognition particle (SRP) when nascent polypeptide chains emerge from the ribosome. The SRP-ribosome nascent chain complex is then targeted through its GTP-dependent interaction with SRP receptor to the protein-conducting channel on endoplasmic reticulum membrane in eukaryotes or plasma membrane in bacteria. A universally conserved component of SRP (refs 1, 2), SRP54 or its bacterial homologue, fifty-four homologue (Ffh), binds the signal peptides, which have a highly divergent sequence divisible into a positively charged n-region, an h-region commonly containing 8-20 hydrophobic residues and a polar c-region. No structure has been reported that exemplifies SRP54 binding of any signal sequence. Here we have produced a fusion protein between Sulfolobus solfataricus SRP54 (Ffh) and a signal peptide connected via a flexible linker. This fusion protein oligomerizes in solution through interaction between the SRP54 and signal peptide moieties belonging to different chains, and it is functional, as demonstrated by its ability to bind SRP RNA and SRP receptor FtsY. We present the crystal structure at 3.5 A resolution of an SRP54-signal peptide complex in the dimer, which reveals how a signal sequence is recognized by SRP54.

Original publication

DOI

10.1038/nature08870

Type

Journal article

Journal

Nature

Publication Date

27/05/2010

Volume

465

Pages

507 - 510

Keywords

Amino Acid Sequence, Bacterial Proteins, Crystallography, X-Ray, Mass Spectrometry, Models, Molecular, Molecular Sequence Data, Protein Binding, Protein Multimerization, Protein Sorting Signals, Protein Structure, Quaternary, Protein Structure, Tertiary, Receptors, Cytoplasmic and Nuclear, Receptors, Virus, Recombinant Fusion Proteins, Signal Recognition Particle, Structure-Activity Relationship, Sulfolobus solfataricus