Jump to content

Whey acidic protein

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Tom.Reding (talk | contribs) at 02:28, 6 June 2016 (WAP motif and cancer: CS1 maintenance: vauthors/veditors or enumerate multiple authors/editors; WP:GenFixes on, using AWB). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

WAP
R-elafin, a specific inhibitor of elastase
(11 NMR structures, PDB: 2REL​)
Identifiers
SymbolWAP
PfamPF00095
Pfam clanCL0454
InterProIPR008197
PROSITEPDOC00026
SCOP21fle / SCOPe / SUPFAM
TCDB1.C.15
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary

In molecular biology, the protein domain Whey acidic protein (WAP) has been identified as a major whey protein in milk and is important in regulating the proliferation of mammary epithelial cells. Additionally, its physiological function is thought to be similar to a protease inhibitor. It has been concluded, therefore, that WAP regulates the proliferation of mammary epithelial cells by preventing elastase-type serine proteases from carrying out laminin degradation and by suppressing the MAP kinase signal pathway in the cell cycle.[1]

Production in mammals

Whey Acidic Protein(WAP) is the major milk protein in certain mammals. There are exceptions in some mammalian species, whereby WAP has not been found to be synthesized in the mammary gland.[1]

WAP motif and cancer

There have been several candidate markers for cancer; most notably genes coding for elafin, antileukoproteinase 1 (previously called secretory leucocyte proteinase inhibitor, SLPI), WAP four disulphide core domain protein 1 (previously called prostate stromal protein 20 kDa, PS20), and WAP four disulphide core domain protein 2 (previously called major human epididymis-specific protein E4, HE4). These genes can be useful biomarkers for detecting tumours.[2]

Furthermore, transcription factor nuclear factor kappa B (NF-κB) is affected, leading to angiogenesis, cell proliferation, invasion and apoptosis.[2]

Biochemistry of WAP motifs

Whey Acidic Protein contains two to three four-disulfide core domain, also termed WAP domain or WAP motif. Each disulfide bond of the WAP motif is made up of two cysteine molecule. This motif is also found in other proteins of different functions, which led to the suggestion that WAP is associated with antiprotease or antibacterial properties. The following schematic representation shows the position of the conserved cysteines that form the 'four-disulfide core' WAP domain

                          +---------------------+
                          |    +-----------+    |
                          |    |           |    |
        xxxxxxxCPxxxxxxxxxCxxxxCxxxxxCxxxxxCCxxxCxxxCxxxx
               |                     |      |       |
               |                     +--------------+
               |                            |
               +----------------------------+
        <------------------50-residues------------------>

'C': conserved cysteine involved in a disulfide bond.

  • WAP-type [1] 'four-disulfide core' domain in PROSITE

It has been found that humans and ruminants have the WAP gene in their genome as pseudogene. Although humans and ruminants do not seem to encode the gene, there is no detrimental effect. However, mouse pups feeding on maternal milk lacking Whey Acidic Protein has been associated with poor growth rate and lethality.

References

  1. ^ a b Seki M, Matsura R, Iwamori T, Nukumi N, Yamanouchi K, Kano K, et al. (2012). "Identification of whey acidic protein (WAP) in dog milk". Exp Anim. 61 (1): 67–70. PMID 22293674.
  2. ^ a b Bouchard D, Morisset D, Bourbonnais Y, Tremblay GM (2006). "Proteins with whey-acidic-protein motifs and cancer". Lancet Oncol. 7 (2): 167–74. doi:10.1016/S1470-2045(06)70579-4. PMID 16455481.