Octyl_glucoside
Octyl glucoside
Chemical compound
Octyl glucoside (n-octyl-β-d-glucoside) is a nonionic surfactant frequently used to solubilise integral membrane proteins for studies in biochemistry. Structurally, it is a glycoside derived from glucose and octanol. Like Genapol X-100 and Triton X-100, it is a nonphysiological amphiphile that makes lipid bilayers less "stiff".[2]
Names | |
---|---|
IUPAC name
Octyl β-D-glucopyranoside | |
Systematic IUPAC name
(2R,3S,4S,5R,6R)-2-(Hydroxymethyl)-6-(octyloxy)oxane-3,4,5-triol | |
Other names
n-Octyl-β-D-glucoside | |
Identifiers | |
3D model (JSmol) |
|
ChemSpider |
|
ECHA InfoCard | 100.045.337 |
EC Number |
|
MeSH | C018619 |
PubChem CID |
|
UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
Properties | |
C14H28O6 | |
Molar mass | 292.37 g/mol |
Surface tension: | |
0.025 M[1] | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
Octyl glucoside has become one of the most important detergents for purification of membrane proteins because it generally does not denature the protein and can readily be removed from final protein extracts.[3] Above its critical micelle concentration of 0.025 M[1] (~0.7% w/v), it was noted as the best detergent for improving selectivity of immunoprecipitation of phosphotyrosine modified proteins.[4] This detergent has also been shown to rapidly inactivate infective HIV at concentrations above its CMC.[5]
The compound gained popularity with researchers following the publication of an improved synthesis in 1978.[6][7] However, in 1990 the cost remained prohibitive for large-scale protein isolation.[8]
Octyl glucoside has been proposed as a conditioning agent to prevent microbial colonization of contact lenses, due to its ability to lower the hydrophobicity of contact lenses and prevent adhesion of Staphylococcus epidermidis and Pseudomonas aeruginosa.[9]
- Shinoda, Kozo; Yamaguchi, Tokio; Hori, Ryohei (1961). "The Surface Tension and the Critical Micelle Concentration in Aqueous Solution of β-D-Alkyl Glucosides and their Mixtures". Bulletin of the Chemical Society of Japan. 34 (2): 237–241. doi:10.1246/bcsj.34.237.
- Lundbaek JA, Birn P, Hansen AJ, Søgaard R, Nielsen C, Girshman J, Bruno MJ, Tape SE, Egebjerg J, Greathouse DV, Mattice GL, Koeppe RE, Andersen OS (May 2004). "Regulation of sodium channel function by bilayer elasticity: the importance of hydrophobic coupling. Effects of Micelle-forming amphiphiles and cholesterol". The Journal of General Physiology. 123 (5): 599–621. doi:10.1085/jgp.200308996. PMC 2234500. PMID 15111647.
- Morandat S, El Kirat K (April 2007). "Solubilization of supported lipid membranes by octyl glucoside observed by time-lapse atomic force microscopy". Colloids and Surfaces. B, Biointerfaces. 55 (2): 179–84. doi:10.1016/j.colsurfb.2006.11.039. PMID 17207975.
- Santos L, Rodrigues D, Lira M, Oliveira R, Real Oliveira ME, Vilar EY, Azeredo J (May 2007). "The effect of octylglucoside and sodium cholate in Staphylococcus epidermidis and Pseudomonas aeruginosa adhesion to soft contact lenses". Optometry and Vision Science. 84 (5): 429–34. doi:10.1097/OPX.0b013e318058a0cc. hdl:1822/6663. PMID 17502827. S2CID 2509161.