A fatty acid is composed of a terminal carboxylate group and a long hydrocarbon chain. Fatty acids exert four major physiological roles in the organism. Firstly, fatty acids serve as building blocks of amphipathic molecules such as phospholipids and glycolipids, which are important components of biological membranes. Secondly, fatty acids can target many proteins to membrane locations by covalently attached to the targeted proteins. Thirdly, stored as triacylglycerols, uncharged esters of fatty acids with glycerol, fatty acids are the preferred fuel molecules for the heart and the preferred energy source for skeletal muscle at the time of prolonged exertion. Triacylglycerols are catabolized into free fatty acid and glycerol. In the liver and peripheral, through β-oxidation, free fatty acid is metabolized into acetyl CoA while glycerol is used for gluconeogenesis or triglyceride regeneration. Finally, fatty acid derivatives act as intracellular messengers and hormones.
The degradation and synthesis of fatty acid are rather simple and they are the reverse of each other. Through the degradation pathway, the aliphatic compound fatty acid is converted to a series of activated acetyl units to enter citric acid cycle and offer energy. Through oxidation, fatty acid is activated and a double bond is introduced. By introducing oxygen, the double bond is hydrated. The alcohol is then oxidized and a ketone is formed. Finally, coenzyme A cleaves the four carbons fragment and acetyl CoA and a fatty acid with chains two carbons shorter are generated. If the fatty acid is saturated and has an even number of carbon atoms, the process will continue till the fatty acid is completely converted to acetyl CoA units. For each two carbons in the fatty acid, 5 ATPs is generated during the oxidation to acetyl CoA and another 12 ATPs through the coenzyme oxidation. Therefore, fatty acid is a rather potent energy store source.
The synthesis of fatty acid is essentially the reverse of this degradation process. The synthesis of fatty acids starts from activated acyl group and malonyl units. The malonyl unit reacts with the acetyl unit and a four-carbon fragment is generated. Exactly the opposite of degradation, the fragment is then reduced, dehydrated, and reduced again, the carbonyl group is then brought to the level of a methylene group and the butyryl CoA is then formed at the same time. Butyryl unit reacts with another activated malonyl group and this process continues till a C18 fatty acid is synthesized.
Since fatty acids metabolism plays a crucial role in large number of disorders like cardiovascular disease and certain types of cancer, the detection and quantification of these compounds are of great importance. Since the endogenous fatty acids metabolites are of rather low concentration, sensitive and specific analytical methods are required for the reliable quantification of these compounds. HPLC-MS/MS has emerged as one of the main techniques used for fatty acids metabolites quantification. Creative Proteomics has established sensitive, reliable, and accurate LC-MS/MS method for quantification of fatty acids metabolites.
- Identification and quantification of fatty acids metabolites by LC-MS/MS.
- Normal Volume: 100ul plasma; 50mg tissue; 2e7 cells
- Minimal Volume: 50uL plasma; 30mg tissue; 5e6 cells
- A detailed technical report will be provided at the end of the whole project, including the experiment procedure, GC-MS instrument parameters.
- Analytes are reported as uM or ug/mg (tissue), and CV's are generally<10%.
- The name of the analytes, abbreviation, formula, molecular weight and CAS# would also be included in the report.
|Fatty Acids Metabolites Quantified in This Service|
|Acetic acid||Acetoacetic acid||Arachidic acid (eicosanoic acid)|
|Arachidonic acid||Behenic acid||Butyric acid|
|Caproic acid||Carnitine (C0 )||Carnitine (C10)|
|Carnitine (C10:1)||Carnitine (C14)||Carnitine (C14:1)|
|Carnitine (C16)||Carnitine (C16-OH)||Carnitine (C18)|
|Carnitine (C18:1)||Carnitine (C18:2)||Carnitine (C18-OH)|
|Carnitine (C2)||Carnitine (C20)||Carnitine (C20:4)|
|Carnitine (C3)||Carnitine (C4)||Carnitine (C5-iso)|
|Carnitine (C6)||Carnitine (C8)||Carnitine (C12)|
|cis-4,7,3,6,9-Docosahexaenoic acid||Decanoic acid||Dodecanoic acid|
|Elaidic acid||Erucic acid||Glutarylcarnitine (C05-DC)|
|Heptanoic acid||Hexanoic acid||Isobutyric acid|
|Isovaleric acid||Lignoceric acid||Linoleic acid|
|Linolenic acid||Malonic acid||Myristic acid|
|Nervonic acid||Octanoic acid||Oleic acid|
|Palmitic acid||Palmitoleic acid||Petroselinic acid|
|Propionic acid||Stearic acid||Valeric acid|
|β-hydroxybutyric acid||2-Methyl butyric acid||3-Metyl valeric acid|
With integrated set of separation, characterization, identification and quantification systems featured with excellent robustness & reproducibility, high and ultra-sensitivity, Creative Proteomics provides reliable, rapid and cost-effective fatty acids metabolism targeted lipidomics services.