Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
22
pubmed:dateCreated
1995-7-19
pubmed:abstractText
Glycerol-3-phosphate acyltransferase (GPAT) catalyzes the initial step in glycerolipid biosynthesis. We recently cloned a cDNA to a 6.8-kb mRNA, a message that can be induced dramatically by feeding a high-carbohydrate diet [Paulauskis & Sul (1988) J. Biol. Chem. 263, 7049-7054; Shin et al. (1991) J. Biol. Chem. 266, 23834-23839], and identified the open reading frame, p90, as mitochondrial GPAT [Yet et al. (1993) Biochemistry 32, 9486-9491]. To initiate characterization of mitochondrial GPAT, we purified and reconstituted the GPAT activity using phospholipids after expressing functional enzyme in Sf9 insect cells. Infection with recombinant virus containing p90 sequence resulted in high levels of GPAT expression in mitochondria, compared to noninfected cells or cells infected with the reverse orientation insertion baculovirus. There was a dramatic increase in N-ethylmaleimide-resistant mitochondrial GPAT activity. The GPAT protein was not detectable by Western blot in noninfected Sf9 cells or in cells infected with the GPAT sequence in the reverse orientation. However, in cells infected with GPAT in the correct orientation, there was a dramatic increase in the GPAT protein that was readily detectable by Coomassie staining both in total extracts and in the mitochondrial fraction. To ease the purification, we next expressed GPAT as a polyhistidine fusion protein in insect cells. The polyhistidine tag did not interfere with targeting to mitochondria or with the catalytic activity of GPAT.(ABSTRACT TRUNCATED AT 250 WORDS)
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0006-2960
pubmed:author
pubmed:issnType
Print
pubmed:day
6
pubmed:volume
34
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
7303-10
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:7779773-Animals, pubmed-meshheading:7779773-Baculoviridae, pubmed-meshheading:7779773-Base Sequence, pubmed-meshheading:7779773-Blotting, Western, pubmed-meshheading:7779773-Cell Line, pubmed-meshheading:7779773-DNA Primers, pubmed-meshheading:7779773-Electrophoresis, Polyacrylamide Gel, pubmed-meshheading:7779773-Ethylmaleimide, pubmed-meshheading:7779773-Gene Expression, pubmed-meshheading:7779773-Glycerol-3-Phosphate O-Acyltransferase, pubmed-meshheading:7779773-Kinetics, pubmed-meshheading:7779773-Mice, pubmed-meshheading:7779773-Mitochondria, pubmed-meshheading:7779773-Molecular Sequence Data, pubmed-meshheading:7779773-Molecular Weight, pubmed-meshheading:7779773-Phospholipids, pubmed-meshheading:7779773-Polymerase Chain Reaction, pubmed-meshheading:7779773-Recombinant Proteins, pubmed-meshheading:7779773-Spodoptera, pubmed-meshheading:7779773-Transfection
pubmed:year
1995
pubmed:articleTitle
Purification and reconstitution of murine mitochondrial glycerol-3-phosphate acyltransferase. Functional expression in baculovirus-infected insect cells.
pubmed:affiliation
Department of Nutritional Sciences, University of California, Berkeley 94720, USA.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't