BDS-1

Blood-depressing substance-1 (BDS-1), also known as kappa-actitoxin-Avd4a, is a polypeptide found in the venom of the snakelocks anemone Anemonia sulcata.[1] BDS-1 is a neurotoxin that modulates voltage-dependent potassium channels, in particular Kv3-family channels, as well as certain sodium channels.[2][3] This polypeptide belongs to the sea anemone type 3 toxin peptide family.[1]

Infobox
BDS-1
Identifiers
OrganismAnemonia sulcata
SynonymKappa-actitoxin-Avd4a
PDB2BDS
UniprotP11494

Etymology

BDS-1 brings about a decrease in blood pressure by blocking Kv3 potassium channels. Thus, this protein is named after its antihypertensive function.[4]

Sources

BDS-1 is a toxin secreted by the nematocyst of Anemonia sulcata (Mediterranean snakelocks sea anemone).[1]

Chemistry

BDS-1 is a 43 amino acids long polypeptide chain, which consists of six cysteines linked by three disulfide bridges. The secondary structure of BDS-1 possesses three-stranded antiparallel β-sheets, along with one more short antiparallel β-sheet at its N-terminus.[5][6] When viewed along the polypeptide strand, its structure showa a right-handed twist.[6]

BDS-1 shares structural homology with the toxin BDS-2, which belongs to the same type-3 peptide family. It also displays around 24–26% identity with toxins AsI (ATX-I), AsII (ATX-II), and AsV (ATX-V) from Anemonia sulcata and AxI (AP-A) from Anthopleura xanthogrammica.[4]

Target

BDS-1 is an inhibitor of the fast inactivating Kv3-family channels, including Kv3.1, Kv3.2 and Kv3.4 channels.[2] Additionally, BDS-1 affects the inactivation of voltage-gated sodium channels, Nav1.1, Nav1.3, Nav1.6 and Nav1.7.[3]

Mode of action

BDS-1 modifies the voltage-dependent gating properties of Kv3 potassium channels by binding to the voltage sensitive domains on S3b and S4 subunits.[2] The toxin elicits a depolarizing shift in the conductance-voltage relation, making it more difficult to open, and slows both the activation and inactivation kinetics of these ion channels.[2]

In addition, BDS-1 enhances the current flowing through several voltage-gated sodium channels. The toxin binds to the S3-S4 linker of domain IV and slows the inactivation of the channel, resulting in increased current upon depolarization. BDS-1 has a very strong potency for the human Nav1.7 channel. In mice, BDS-1 slows the inactivation of Nav1.3 channels but has smaller effects on the inactivation of Nav1.1 and Nav1.6 channels. This is probably due to a different channel sensitivity for the toxin.[3]

Toxicity

By targeting Kv3.1a channels, BDS-1 concentrations at or above 3 μM are toxic to mouse fibroblasts.[2]

References

  1. "UniProtKB - P11494 (BDS1_ANESU)".
  2. Yeung, Shuk Yin M.; et al. (2005). "Modulation of Kv3 subfamily potassium currents by the sea anemone toxin BDS: significance for CNS and biophysical studies". Journal of Neuroscience. 25 (38): 8735–45. doi:10.1523/JNEUROSCI.2119-05.2005. PMC 1314979. PMID 16177043.
  3. Liu, Pin; Sooyeon Jo & Bruce P. Bean (2012). "Modulation of neuronal sodium channels by the sea anemone peptide BDS-I". Journal of Neurophysiology. 107 (11): 3155–67. doi:10.1152/jn.00785.2011. PMC 3378363. PMID 22442564.
  4. Diochot, Sylvie; et al. (1998). "Sea anemone peptides with a specific blocking activity against the fast inactivating potassium channel Kv3. 4". Journal of Biological Chemistry. 273 (12): 6744–9. doi:10.1074/jbc.273.12.6744. PMID 9506974.
  5. Frazão, Bárbara; Vitor Vasconcelos & Agostinho Antunes (2012). "Sea anemone (Cnidaria, Anthozoa, Actiniaria) toxins: an overview". Marine Drugs. 10 (12): 1812–51. doi:10.3390/md10081812. PMC 3447340. PMID 23015776.
  6. Driscoll, Paul C.; et al. (1989). "A proton nuclear magnetic resonance study of the antihypertensive and antiviral protein BDS-I from the sea anemone Anemonia sulcata: sequential and stereospecific resonance assignment and secondary structure". Biochemistry. 28 (5): 2178–87. doi:10.1021/bi00431a032. PMID 2566325.
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