Abstract
A method is described for the assay of lipoprotein lipase, using a stable, radioactive substrate emulsion. Fatty acid-labeled trioleoylglycerol was emulsified by homogenization in glycerol with lecithin as detergent. This anhydrous emulsion was stable for at least six weeks. Substrate solutions for enzyme assay were prepared by diluting the emulsion with buffer containing serum and albumin. The fatty acid produced on hydrolysis was isolated in a one-step liquid-liquid partition system. Incubations with extracts of acetone powders from adipose tissue displayed characteristics of lipoprotein lipase activity, i.e., serum dependence and inhibition by NaCl and protamine. The method is rapid (less than 1 hour), sensitive and reproducible, and suitable for routine use.
| Original language | English |
|---|---|
| Pages (from-to) | 536-541 |
| Journal | Journal of Lipid Research |
| Volume | 17 |
| Issue number | 5 |
| Publication status | Published - 1976 |
| Externally published | Yes |
Subject classification (UKÄ)
- Medicinal Chemistry
- Pharmacology and Toxicology
Free keywords
- adipose lipoprotein lipase tri[3H]oleoylglycerol
- triglyceride
- postheparin serum