Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
1980-6-25
pubmed:abstractText
The fluorescent phospholipid dansyl phosphatidylethanolamine (DPE) (dansyl, 5-dimethylaminonaphthalene-1-sulfonyl) was incorporated into very low density lipoproteins (VLDL) to form DPE-VLDL. The addition of milk lipoprotein lipase to DPE-VLDL in the presence of albumin resulted in a greater than 3-fold fluorescence increase and a 20 nm blue shift in the wavelength of the emission maxima of the dansyl fluorophore. The lipoprotein lipase-induced fluorescence changes occurred concomitantly with the release of free fatty acids from VLDL. Lipoprotein lipase did not produce fluorescence changes in DPE incorporated into either low or high density lipoproteins. The rate of fluorescence increase in DPE-VLDL was maximal at 37 degrees C, dependent on the concentration of lipoprotein lipase and VLDL, and followed typical Michaelis-Menten kinetics with a Km of 1.0 for lipoprotein lipase. Both the initial rate and the total fluorescence increase correlated well (r = 0.98 and 0.95) with the release of free fatty acids. We conclude that the lipoprotein lipase-induced fluorescence increases in DPE-VLDL provide an accurate, convenient, and the only noninvasive means of following continuously the lipolysis of human VLDL.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
25
pubmed:volume
255
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3461-5
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed:year
1980
pubmed:articleTitle
Dansyl phosphatidylethanolamine-labeled very low density lipoproteins. A fluorescent probe for monitoring lipolysis.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.