Signal peptide

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A signal peptide is a short (3-60 amino acids long) peptide chain that directs the post-translational transport of a protein. Signal peptides may also be called targeting signals, signal sequences, transit peptides, or localization signals.

The amino acid sequences of signal peptides direct proteins (which are synthesized in the cytosol) to certain organelles such as the nucleus, mitochondrial matrix, endoplasmic reticulum, chloroplast, apoplast and peroxisome. Some signal peptides are cleaved from the protein by signal peptidase after the proteins are transported.

ER signal peptide

An endoplasmic reticulum signal peptide is the best characterized signal peptide. It exists at the amino terminal of a protein. The protein is guided to the ER by a signal-recognition particle (SRP), which moves between the ER and the cytoplasm. It binds to the signal peptide. The SRP binds to the signal peptide as soon as it is synthesised and extruded from the ribosome. This causes a pause in protein synthesis, most probably allowing the ribosome-SRP complex time to bind to the SRP receptor on the target ER membrane. The SRP protein is thought to be a regulatory GTP protein. Conformational changes may therefore lead to the SRP release. The protein may then be threaded through the ER membrane by a translocator pore.

Nuclear signal peptides

A nuclear localization signal (NLS) is a signal peptide directing to the nucleus and is often a unit consisting of plus-charged amino acids. The NLS normally is located inside the peptide chain. Almost all proteins that are transported to the endoplasmic reticulum have a sequence consisting of 5-10 hydrophobic amino acids on the N-terminus. Most of these proteins are transported from the endoplasmic reticulum to the Golgi apparatus. If these proteins have a particular 4-amino-acids sequence on the C-terminus, these proteins stay in the endoplasmic reticulum.

The nucleolus within the nucleus can be targeted with a sequence called a nucleolar localization signal (abbreviated NoLS or NOS).

The signal peptide that directs to the mitochondrial matrix has a sequence consisting of an alternating pattern with a few hydrophobic amino acids and a few plus-charged amino acids form. It is usually called the mitochondrial targeting signal (MTS).

There are two types of signal peptides directing to peroxisome, which are called peroxisomal targeting signals (PTS). One is PTS1, which is made of three amino acids on the C-terminus. The other is PTS2, which is made of a 9-amino-acid sequence often present on the N-terminus of the protein.

Types

Following is a list of types of signal peptides:

Typical signal peptides

Transport to the nucleus (NLS)            -Pro-Pro-Lys-Lys-Lys-Arg-Lys-Val-
 
Transport to the endoplasmic reticulum    H2N-Met-Met-Ser-Phe-Val-Ser-Leu-
                                              Leu-Leu-Val-Gly-Ile-Leu-Phe-
                                              Trp-Ala-Thr-Glu-Ala-Glu-Gln-
                                              Leu-Thr-Lys-Cys-Glu-Val-Phe-
                                              Gln-
 
Retention to the endoplasmic reticulum    -Lys-Asp-Glu-Leu-COOH
 
Transport to the mitochondrial matrix     H2N-Met-Leu-Ser-Leu-Arg-Gln-Ser-
                                              Ile-Arg-Phe-Phe-Lys-Pro-Ala-
                                              Thr-Arg-Thr-Leu-Cys-Ser-Ser-
                                              Arg-Tyr-Leu-Leu-
 
Transport to the peroxisome (PTS1)        -Ser-Lys-Leu-COOH
 
Transport to the peroxisome (PTS2)        H2N-----Arg-Leu-X5-His-Leu-
 

H2N is the N-terminus of a protein. COOH is the C-Terminus of a protein.

See also

External links


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Acknowledgement and Attribution Regarding Sources of Content

Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

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