Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2007-10-15
pubmed:abstractText
We describe a sensitive assay for detection of active hyaluronan synthases (HASs) capable of synthesizing hyaluronan (HA) without use of radioactive uridine 5'-diphosphate sugar precursors. The HAS capture assay is based on the binding of a biotinylated HA binding protein (bHABP) to HA chains that are associated with HAS and the subsequent capture of bHABP-HA-HAS complexes with streptavidin-agarose. Specific HAS proteins (e.g., HAS1, not HAS2 or HAS3) captured in this pull-down approach are readily immunodetected by Western blot analysis using appropriate antibodies. The assay was used to detect active HAS proteins in cell membranes, purified recombinant Streptococcus equisimilis HAS (SeHAS), and in vitro translated human HAS1 or SeHAS. The HAS capture assay was also used to assess the fraction of HAS molecules that were active, which cannot be done using standard assays for synthase activity. Assay sensitivity for detection of purified SeHAS is <1 pmol.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Bacterial Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Edetic Acid, http://linkedlifedata.com/resource/pubmed/chemical/Glucuronosyltransferase, http://linkedlifedata.com/resource/pubmed/chemical/HAS1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Hyaluronic Acid, http://linkedlifedata.com/resource/pubmed/chemical/Isoenzymes, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Sepharose, http://linkedlifedata.com/resource/pubmed/chemical/Transferases, http://linkedlifedata.com/resource/pubmed/chemical/Uridine Diphosphate, http://linkedlifedata.com/resource/pubmed/chemical/hyaluronan synthase, http://linkedlifedata.com/resource/pubmed/chemical/streptavidin-agarose
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0003-2697
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
371
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
62-70
pubmed:meshHeading
pubmed-meshheading:17904513-Bacterial Proteins, pubmed-meshheading:17904513-Biotinylation, pubmed-meshheading:17904513-Blotting, Western, pubmed-meshheading:17904513-Carrier Proteins, pubmed-meshheading:17904513-Cell Membrane, pubmed-meshheading:17904513-Cloning, Molecular, pubmed-meshheading:17904513-Edetic Acid, pubmed-meshheading:17904513-Escherichia coli, pubmed-meshheading:17904513-Glucuronosyltransferase, pubmed-meshheading:17904513-Humans, pubmed-meshheading:17904513-Hyaluronic Acid, pubmed-meshheading:17904513-Isoenzymes, pubmed-meshheading:17904513-Kinetics, pubmed-meshheading:17904513-Membrane Proteins, pubmed-meshheading:17904513-RNA, Messenger, pubmed-meshheading:17904513-Recombinant Proteins, pubmed-meshheading:17904513-Sensitivity and Specificity, pubmed-meshheading:17904513-Sepharose, pubmed-meshheading:17904513-Streptococcus equi, pubmed-meshheading:17904513-Transferases, pubmed-meshheading:17904513-Uridine Diphosphate
pubmed:year
2007
pubmed:articleTitle
An enzyme capture assay for analysis of active hyaluronan synthases.
pubmed:affiliation
Department of Biochemistry & Molecular Biology and The Oklahoma Center for Medical Glycobiology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73190, USA.
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural