TRPP

Family of transport proteins

TRPP (transient receptor potential polycystic) is a family of transient receptor potential ion channels which when mutated can cause polycystic kidney disease.

Subcategories

TRPP subunits can be divided into two subcategories depending on structural similarity.

Polycystic Kidney Disease 1 (PKD1)-Like Group

The first group, polycystic kidney disease 1 (PKD1)-like, contains polycystin-1 (Previously known as TRPP1), PKDREJ, PKD1L1, PKD1L2, and PKD1L3. Polycystin-1 contains numerous N-terminal adhesive domains that are important for cell-cell contact.[1] This group of subunits also contain a large extracellular domain with numerous polycystin motifs. These motifs are of unknown function and are located between the S6 and S7 segments. The large intracellular C-terminal segment of TRPP1 seems to interact with TRPP2 to act as a signaling complex.[2]

Polycystic Kidney Disease 2 (PKD2)-Like Group

This group of TRPP members (previously known as TRPP2-like) are: TRPP1 (previously known as TRPP2 or PKD2), TRPP2 (previously known as TRPP3 or PKDL2), and TRPP3 (previously known as TRPP5 or polycystin-L2).[3] Unlike the previous group, which contain 11 membrane-spanning segments, this group resemble other TRP channels, having 6 membrane-spanning segments with intracellular N- and C-termini. All of the members of this group contain a coiled coil region in their C-terminus involved in the interaction with the polycystin-1 group. TRPP1 and TRPP3 form constitutively active cation-selective ion channels that are permeable to calcium. TRPP2 has also been implicated in sour taste perception. Coupling of PKD1 and TRPP1 recruits TRPP1 to the membrane. Here, its activity is decreased and it suppresses the activation of G proteins by PKD1.[2]

Genes

  • Group 1: polycystic kidney disease 1 (PKD1) like proteins
    • PKD1 PKD1
    • PKDREJ
    • PKD1L1
    • PKD1L2
    • PKD1L3
  • Group 2: polycystic kidney disease 2 (PKD2) like proteins
    • TRPP1 PKD2
    • TRPP2 PKD2L1
    • TRPP3 PKD2L2

See also

  • Polycystic kidney disease

References

  1. ^ Islam, M. S. Transient Receptor Potential Channels. Advances in Experimental Medicine and Biology. Vol 704. ISBN 978-94-007-0264-6
  2. ^ a b Nilius B, Owsianik G, Voets T, Peters JA (2007). "Transient receptor potential cation channels in disease" (PDF). Physiol. Rev. 87 (1): 165–217. doi:10.1152/physrev.00021.2006. PMID 17237345.
  3. ^ *"Transient Receptor Potential Channels". IUPHAR Database of Receptors and Ion Channels. International Union of Basic and Clinical Pharmacology.

External links

  • TRPP+Cation+Channels at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
  • "Transient Receptor Potential Channels". IUPHAR Database of Receptors and Ion Channels. International Union of Basic and Clinical Pharmacology.
  • "TRIP Database". a manually curated database of protein-protein interactions for mammalian TRP channels.
  • v
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Membrane transport protein: ion channels (TC 1A)
Ca2+: Calcium channel
Ligand-gated
  • Inositol trisphosphate receptor
    • 1
    • 2
    • 3
  • Ryanodine receptor
Voltage-gated
Constitutively active
Proton-gated
Voltage-gated
Calcium-activated
Inward-rectifier
Tandem pore domain
Voltage-gated
Miscellaneous
Cl: Chloride channel
H+: Proton channel
M+: CNG cation channel
M+: TRP cation channel
H2O (+ solutes): Porin
Cytoplasm: Gap junction
By gating mechanism
Ion channel class
see also disorders
  • v
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  • e
TRP channel modulators
TRPA
Activators
Blockers
TRPC
Activators
Blockers
TRPM
Activators
Blockers
TRPML
Activators
Blockers
TRPP
Activators
Blockers
TRPV
Activators
Blockers
See also: Receptor/signaling modulators • Ion channel modulators