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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
1993-10-13
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pubmed:abstractText |
6-O-[(2-Hydroxyethyl)poly(2-oxyethyl)]chitosan ("glycolchitosan") was oxidatively cleaved with nitrous acid and then partly acetylated with acetic anhydride, reacted with bromoacetyl-N-hydroxysuccinimide, and reacted further with acetic anhydride. Conditions were selected, including fractionation by size-exclusion chromatography, so that the resulting "Chitin Leash" had an estimated, average molecular weight of 10,000 (dextran standards), corresponding to a length of approximately 40 sugar residues. It possessed 0.9 terminal aldehyde and 2.6 random (presumably) side-chain bromoacetyl reactive groups per chain (average values). As a model system, the Chitin Leash was used to crosslink staphylococcal nuclease (SNase) to ribonuclease A (RNase) with retention of 75 and 78%, respectively, of the starting enzyme activities. For this coupling, the Nase was first converted to a sulfhydryl SNase derivative which retained 74% of the activity of starting enzyme. The yields in this synthesis were: 13% Chitin Leash from glycolchitosan, 24% Chitin Leash-RNase from Chitin Leash and 45% SNase-Chitin Leash-RNase from the latter conjugate. The ratio of SNase to RNase in this conjugate was 1.0:0.94. In a second preparation, in which [14C]acetic anhydride was used, a longer reaction time was employed for the coupling of Chitin Leash to RNase. This gave a 1.0:1.8:0.95 molar ratio of Nase: [14C]Chitin Leash: RNase, revealing multiple attachment of the [14C]Chitin Leash to RNase. The activity of the RNase in the final conjugate was 20%. The latter conjugate was approximately 70% hydrolyzed by diaminooctyl-succinyl-lysozyme, disconnecting the two enzymes while not affecting their activities.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Chitin,
http://linkedlifedata.com/resource/pubmed/chemical/Chitosan,
http://linkedlifedata.com/resource/pubmed/chemical/Cross-Linking Reagents,
http://linkedlifedata.com/resource/pubmed/chemical/Micrococcal Nuclease,
http://linkedlifedata.com/resource/pubmed/chemical/Muramidase,
http://linkedlifedata.com/resource/pubmed/chemical/Nitrous Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Ribonuclease, Pancreatic
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0008-6215
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
17
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pubmed:volume |
246
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
205-17
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:8370039-Carbohydrate Sequence,
pubmed-meshheading:8370039-Chitin,
pubmed-meshheading:8370039-Chitosan,
pubmed-meshheading:8370039-Cross-Linking Reagents,
pubmed-meshheading:8370039-Micrococcal Nuclease,
pubmed-meshheading:8370039-Molecular Sequence Data,
pubmed-meshheading:8370039-Muramidase,
pubmed-meshheading:8370039-Nitrous Acid,
pubmed-meshheading:8370039-Oxidation-Reduction,
pubmed-meshheading:8370039-Ribonuclease, Pancreatic
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pubmed:year |
1993
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pubmed:articleTitle |
"Chitin Leash": a polysaccharide heterobifunctional cross-linking agent which can be cleaved by lysozyme.
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pubmed:affiliation |
Department of Pharmaceutical Sciences, College of Pharmacy and Allied Health Professions, Northeastern University, Boston, MA 02115.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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