Brefeldin A

Brefeldin A
Names
IUPAC name
(1R,2E,6S,10E,11aS,13S,14aR)-1,13-Dihydroxy-6-methyl-1,6,7,8,9,11a,12,13,14,14a-decahydro-4H-cyclopenta[f]oxacyclotridecin-4-one
Other names
γ,4-Dihydroxy-2-(6-hydroxy-1-heptenyl)-4-cyclopentanecrotonic acid λ-lactone
Identifiers
20350-15-6 YesY
3D model (Jmol) Interactive image
ChEBI CHEBI:48080 YesY
ChEMBL ChEMBL19980 YesY
ChemSpider 4449949 YesY
DrugBank DB07348 YesY
ECHA InfoCard 100.127.053
PubChem 5287620
Properties
C16H24O4
Molar mass 280.36 g/mol
Appearance White to off-white crystalline powder
Melting point 204 to 205 °C (399 to 401 °F; 477 to 478 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Brefeldin A is a lactone antibiotic produced by fungal organisms such as Eupenicillium brefeldianum.[1] Brefeldin A inhibits protein transport from the endoplasmic reticulum to the Golgi apparatus indirectly by preventing formation of COPI-mediated[2] transport vesicles. Brefeldin A was initially isolated as an anti-viral antibiotic[3] but is now primarily used in biological research to study protein transport.

Physical data

Brefeldin A forms a clear colorless solution at 10 mg/ml in both dichloromethane and methanol.[4]

Biological effects

In mammalian and yeast cells, the main target of brefeldin A appears to be a Guanine nucleotide exchange factor called GBF1.[5] GBF1 mediates formation of transport vesicles by recruiting COPI coat proteins to cargo-bound receptor proteins found in the membrane of the Golgi. Inhibition of GBF1 activity induced the retrograde movement of secretory proteins from the golgi to the ER. The collapse of the Golgi into the ER triggers activation of unfolded protein response (UPR) (or ER stress)[6][7] which can result in apoptosis.

See also

References

  1. ↑ Hutchinson, C. R.; Shu-Wen, L.; McInnes, A. G.; Walter, J. A. (1983). "Comparative biochemistry of fatty acid and macrolide antibiotic (brefeldin a). Formation in penicillium brefeldianum". Tetrahedron. 39 (21): 3507. doi:10.1016/S0040-4020(01)88660-9.
  2. ↑ http://www.cellsignal.com/pdf/9972.pdf
  3. ↑ Tamura G, Ando K, Suzuki S, Takatsuki A, Arima K (February 1968). "Antiviral activity of brefeldin A and verrucarin A". J. Antibiot. 21 (2): 160–1. doi:10.7164/antibiotics.21.160. PMID 4299889.
  4. ↑ Brefeldin A Archived June 26, 2006, at the Wayback Machine. product page from Fermentek
  5. ↑ http://www.genecards.org/cgi-bin/carddisp.pl?gene=GBF1
  6. ↑ Pahl HL, Baeuerle (Jun 1995). "A novel signal transduction pathway from the endoplasmic reticulum to the nucleus is mediated by transcription factor NF-kappa B". EMBO J. 14 (11): 2580–8. PMID 7781611.
  7. ↑ Kober L, Zehe C, Bode J (October 2012). "Development of a novel ER stress based selection system for the isolation of highly productive clones". Biotechnol. Bioeng. 109 (10): 2599–611. doi:10.1002/bit.24527. PMID 22510960.
Wikimedia Commons has media related to Brefeldin A.
This article is issued from Wikipedia - version of the 11/18/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.