Proteomic amino-termini profiling reveals targeting information for protein import into complex plastids.

Proteomic amino-termini profiling reveals targeting information for protein import into complex plastids.

Blog Article

In organisms with complex plastids acquired by secondary endosymbiosis from a photosynthetic eukaryote, the majority of plastid proteins are nuclear-encoded, translated on cytoplasmic ribosomes, and guided across four membranes by a bipartite targeting sequence.In-depth understanding of this vital import process has been impeded Rests by a lack of information about the transit peptide part of this sequence, which mediates transport across the inner three membranes.We determined the mature N-termini of hundreds of proteins from the model diatom Thalassiosira pseudonana, revealing extensive N-terminal modification by acetylation and proteolytic processing in both cytosol and plastid.

We identified 63 mature N-termini Dome Cameras of nucleus-encoded plastid proteins, deduced their complete transit peptide sequences, determined a consensus motif for their cleavage by the stromal processing peptidase, and found evidence for subsequent processing by a plastid methionine aminopeptidase.The cleavage motif differs from that of higher plants, but is shared with other eukaryotes with complex plastids.