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Single-pass membrane protein

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Schematic representation of transmembrane proteins: 1. a protein with single transmembrane α-helix (a single-pass membrane protein) (bitopic) 2. a polytopic transmembrane α-helical protein 3. a polytopic transmembrane β-sheet protein
The membrane is represented in yellow.

A single-pass membrane protein also known as single-spanning protein or bitopic protein is a transmembrane protein that spans the lipid bilayer only once.[1][2] These proteins may constitute up to 50% of all transmembrane proteins, depending on the organism, and contribute significantly to the network of interactions between different proteins in cells, including interactions via transmembrane alpha helices.[3] They usually include one or several water-soluble domains situated at the different sides of biological membranes, for example in single-pass transmembrane receptors. Some of them are small and serve as regulatory or structure-stabilizing subunits in large multi-protein transmembrane complexes, such as photosystems or the respiratory chain. A 2013 estimate identified about 1300 single-pass membrane proteins in the human genome.[4]

Topology-based classification

See also: Transmembrane protein § Classification by topology

Bitopic proteins are classified into 4 types, depending on their transmembrane topology and location of the transmembrane helix in the amino acid sequence of the protein. According to Uniprot:

  • Type I: N-terminus on the extracellular side of the membrane; removed signal peptide[5]
  • Type II: N-terminus on the cytoplasmic side of the membrane; transmembrane helix located close to the N-terminus, where it works as an anchor[6]
  • Type III: N-terminus on the extracellular side of the membrane; no signal peptide[7]
  • Type IV: N-terminus on the cytoplasmic side of the membrane; transmembrane helix located close to the C-terminus, where it works as an anchor[8]

Hence type I proteins are anchored to the lipid membrane with a stop-transfer anchor sequence and have their N-terminal domains targeted to the ER lumen during synthesis. Type II and III are anchored with a signal-anchor sequence, with type II being targeted to the ER lumen with its C-terminal domain, while type III have their N-terminal domains targeted to the ER lumen.

Structure

A single-pass transmembrane protein typically consists of three domains, the extracellular domain, the transmembrane domain, and the intracellular domain. The transmembrane domain is the smallest at around 25 amino acid residues and forms an alpha helix inserted into the membrane bilayer. The ECD is typically much larger than the ICD and is often globular, whereas many ICDs have relatively high disorder.[9] Some proteins in this class function as monomers, but dimerization or higher-order oligomerization is common.[9][10]

Evolution

The number of single-pass transmembrane proteins in an organism's genome varies significantly. It is higher in eukaryotes than prokaryotes and in multicellular than unicellular organisms.[11] The fraction of proteins in this class is larger in humans than in the model organisms Danio rerio (zebrafish) and Caenorhabditis elegans (nematode worms), suggesting that genes encoding these proteins have undergone expansion in the vertebrate and mammalian lineages.[4]

Databases

References

  1. ^ "Single-pass membrane protein". www.uniprot.org.
  2. ^ Membrane Structural Biology: With Biochemical and Biophysical Foundations, by Mary Luckey, 2014, Cambridge University Press, page 91.
  3. ^ Zviling, Moti; Kochva, Uzi; Arkin, Isaiah T. (2007). "How important are transmembrane helices of bitopic membrane proteins?". Biochimica et Biophysica Acta (BBA) - Biomembranes. 1768 (3): 387–392. doi:10.1016/j.bbamem.2006.11.019. PMID 17258687.
  4. ^ a b Pahl, Matthew C; Askinazi, Olga L; Hamilton, Catherine; Cheng, Irene; Cichewicz, Karol; Kuhn, Jason; Manohar, Sumanth; Deppmann, Christopher D (2013-10-18). "Signalling via Single-Pass Transmembrane Proteins". eLS: a0025160. doi:10.1002/9780470015902.a0025160.
  5. ^ "Single-pass type I membrane protein". UniProt. Retrieved 15 June 2021.
  6. ^ "Single-pass type II membrane protein". UniProt. Retrieved 15 June 2021.
  7. ^ "Single-pass type III membrane protein". UniProt. Retrieved 15 June 2021.
  8. ^ "Single-pass type IV membrane protein". UniProt. Retrieved 15 June 2021.
  9. ^ a b Bugge, Katrine; Lindorff‐Larsen, Kresten; Kragelund, Birthe B. (December 2016). "Understanding single‐pass transmembrane receptor signaling from a structural viewpoint—what are we missing?" (PDF). The FEBS Journal. 283 (24): 4424–4451. doi:10.1111/febs.13793.
  10. ^ Valley, Christopher C.; Lewis, Andrew K.; Sachs, Jonathan N. (September 2017). "Piecing it together: Unraveling the elusive structure-function relationship in single-pass membrane receptors". Biochimica et Biophysica Acta (BBA) - Biomembranes. 1859 (9): 1398–1416. doi:10.1016/j.bbamem.2017.01.016. PMC 5487282.
  11. ^ Pogozheva, Irina D.; Lomize, Andrei L. (February 2018). "Evolution and adaptation of single-pass transmembrane proteins". Biochimica et Biophysica Acta (BBA) - Biomembranes. 1860 (2): 364–377. doi:10.1016/j.bbamem.2017.11.002.
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