Source:http://linkedlifedata.com/resource/pubmed/id/11427161
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
5
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| pubmed:dateCreated |
2001-6-27
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| pubmed:abstractText |
The mammalian sperm hyaluronidase, PH-20, is active in macaque spermatozoa at neutral and acid pH. Antibodies were produced to synthesized peptides representing regions of PH-20 that may be involved in hyaluronidase activity and designated peptide 1 (amino acid sequence 142-172) and peptide 3 (amino acid sequence 277-297). Western blotting of proteins extracted from the surface of acrosome-intact spermatozoa showed that the two peptide-specific, affinity-purified IgGs label a 64 kDa band corresponding to the PH-20 molecule. Western blots of acrosome-reacted spermatozoa showed that, under reducing conditions, the two anti-peptide IgGs label the 44 kDa band only, which represents the N-terminal fragment of PH-20. Anti-peptide 3 IgG also labels the 53 kDa form of PH-20 in extracts of acrosome-reacted spermatozoa. Peptide-specific, affinity-purified Fab fragments from both IgGs were shown by fluorescence microscopy and transmission electron microscopy to label the sperm plasma membrane, fused acrosomal vesicles, acrosomal matrix and inner acrosomal membrane. Fab fragments of anti-peptide 1 IgG, but not anti-peptide 3 IgG, inhibited hyaluronidase activity of PH-20 from the sperm surface and from extracts of acrosome-reacted spermatozoa at pH 7.0. Fab fragments of both anti-peptide IgGs inhibited sperm hyaluronidase activity at pH 5.0. It is concluded that the region of PH-20 encompassed by the amino acid sequence 142-172 is essential for hyaluronidase activity at neutral pH, whereas the region of amino acid sequence 277-297 may be more important at a lower pH. It is likely that these two regions are the acid/base catalyst site and the nucleophilic site, respectively, of PH-20 hyaluronidases.
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| pubmed:grant | |
| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:citationSubset |
IM
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| pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cell Adhesion Molecules,
http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Hyaluronoglucosaminidase,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin Fab Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/hyaluronidase PH-20
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| pubmed:status |
MEDLINE
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| pubmed:month |
May
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| pubmed:issn |
1470-1626
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| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
121
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| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
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| pubmed:pagination |
735-43
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| pubmed:dateRevised |
2010-4-1
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| pubmed:meshHeading |
pubmed-meshheading:11427161-Acrosome Reaction,
pubmed-meshheading:11427161-Amino Acid Sequence,
pubmed-meshheading:11427161-Animals,
pubmed-meshheading:11427161-Antibody Specificity,
pubmed-meshheading:11427161-Binding Sites,
pubmed-meshheading:11427161-Blotting, Western,
pubmed-meshheading:11427161-Cell Adhesion Molecules,
pubmed-meshheading:11427161-Cell Membrane,
pubmed-meshheading:11427161-Enzyme Inhibitors,
pubmed-meshheading:11427161-Hyaluronoglucosaminidase,
pubmed-meshheading:11427161-Hydrogen-Ion Concentration,
pubmed-meshheading:11427161-Immunoglobulin Fab Fragments,
pubmed-meshheading:11427161-Immunoglobulin G,
pubmed-meshheading:11427161-Macaca fascicularis,
pubmed-meshheading:11427161-Male,
pubmed-meshheading:11427161-Microscopy, Electron,
pubmed-meshheading:11427161-Microscopy, Fluorescence,
pubmed-meshheading:11427161-Molecular Sequence Data,
pubmed-meshheading:11427161-Peptide Fragments,
pubmed-meshheading:11427161-Recombinant Proteins,
pubmed-meshheading:11427161-Spermatozoa,
pubmed-meshheading:11427161-Structure-Activity Relationship
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| pubmed:year |
2001
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| pubmed:articleTitle |
Characterization of the active site of monkey sperm hyaluronidase.
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| pubmed:affiliation |
Division of Reproductive Biology, Department of Obstetrics and Gynecology, University of California, Davis, CA, USA.
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| pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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