Anaphylatoxin

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Anaphylotoxin-like domain
PDB 1c5a EBI.jpg
Structure of porcine C5adesArg.[1]
Identifiers
Symbol ANATO
Pfam PF01821
InterPro IPR000020
SMART ANATO
PROSITE PDOC00906
SCOP 1c5a
SUPERFAMILY 1c5a

Anaphylatoxins, or complement peptides, are fragments (C3a, C4a and C5a) that are produced as part of the activation of the complement system.[2] Complement components C3, C4 and C5 are large glycoproteins that have important functions in the immune response and host defense.[3] They have a wide variety of biological activities and are proteolytically activated by cleavage at a specific site, forming a- and b-fragments.[4] A-fragments form distinct structural domains of approximately 76 amino acids, coded for by a single exon within the complement protein gene. The C3a, C4a and C5a components are referred to as anaphylatoxins:[4][5] they cause smooth muscle contraction, histamine release from mast cells, and enhanced vascular permeability.[5] They also mediate chemotaxis, inflammation, and generation of cytotoxic oxygen radicals.[5] The proteins are highly hydrophilic, with a mainly alpha-helical structure held together by 3 disulfide bridges.[5]

Function[edit]

Anaphylatoxins are able to trigger degranulation (release of substances) of endothelial cells, mast cells or phagocytes, which produce a local inflammatory response. If the degranulation is widespread, it can cause a shock-like syndrome similar to that of an allergic reaction.

Anaphylatoxins indirectly mediate:

Examples[edit]

Important anaphylatoxins:

  • C5a has the highest specific biological activity and is able to act directly on neutrophils and monocytes to speed up the phagocytosis of pathogens.
  • C3a works with C5a to activate mast cells, recruit antibody, complement and phagocytic cells and increase fluid in the tissue, all of which contribute to the initiation of the adaptive immune response.
  • C4a is the least active anaphylatoxin.

Terminology[edit]

Although some drugs (morphine, codeine, synthetic ACTH) and some neurotransmitters (norepinephrine, substance P) are important mediators of degranulation of mast cells or basophils, they are generally not called anaphylatoxins. This term is reserved only for fragments of the complement system.

Human proteins containing this domain[edit]

C3, C4A, C4B, C4B-1, C5, FBLN1, FBLN2

See also[edit]

References[edit]

  1. ^ Williamson MP, Madison VS (March 1990). "Three-dimensional structure of porcine C5adesArg from 1H nuclear magnetic resonance data". Biochemistry 29 (12): 2895–905. doi:10.1021/bi00464a002. PMID 2337573. 
  2. ^ Hugli TE (1986). "Biochemistry and biology of anaphylatoxins". Complement 3 (3): 111–27. PMID 3542363. 
  3. ^ Fritzinger DC, Petrella EC, Connelly MB, Bredehorst R, Vogel CW (1992). "Primary structure of cobra complement component C3". J. Immunol. 149 (11): 3554–3562. PMID 1431125. 
  4. ^ a b Rosa PA, Ogata RT, Zepf NE (1989). "Sequence of the gene for murine complement component C4". J. Biol. Chem. 264 (28): 16565–16572. PMID 2777798. 
  5. ^ a b c d Gennaro R, Simonic T, Negri A, Mottola C, Secchi C, Ronchi S, Romeo D (1986). "C5a fragment of bovine complement. Purification, bioassays, amino-acid sequence and other structural studies". Eur. J. Biochem. 155 (1): 77–86. doi:10.1111/j.1432-1033.1986.tb09460.x. PMID 3081348. 

Janeway et al. Immunobiology Garland Science Publishing 2005

External links[edit]

This article incorporates text from the public domain Pfam and InterPro IPR000020