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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
1990-1-25
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pubmed:abstractText |
Different experimental conditions and chromatographic supports have been selected for the most efficient and rapid purification of procarboxypeptidases from porcine and human pancreas by different high-performance liquid chromatography (HPLC) variants (anion exchange, reversed phase and gel filtration). Anion-exchange chromatography was found to be the most capable and permitted the isolation, in a single step, of three different porcine procarboxypeptidases (2A + 1B forms) and five different human procarboxypeptidases (2B + 3A forms) in a native and pure state from whole pancreas extracts. Other pancreatic proproteases are also cleanly isolated in the same step. Reversed-phase chromatography under mild conditions separated porcine or human procarboxypeptidases A from other pancreatic proteins in a very short time but was unable further to subfractionate the same proteins. The sequential use of gel filtration (or anion-exchange) and reversed-phase HPLC chromatography permitted, in a simple way, the isolation and dissociation of the strongly bound components of the binary complexes between procarboxypeptidases A and proproteinase E in either porcine or human pancreas extracts. Chromatofocusing on a fast protein liquid chromatographic support was also found to be a very efficient technique, showing a slightly lower capability to separate procarboxypeptidases than anion-exchange HPLC though in a much shorter time and in larger quantities.
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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/Carboxypeptidase B,
http://linkedlifedata.com/resource/pubmed/chemical/Carboxypeptidases,
http://linkedlifedata.com/resource/pubmed/chemical/Carboxypeptidases A,
http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Precursors,
http://linkedlifedata.com/resource/pubmed/chemical/Multienzyme Complexes
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0021-9673
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
3
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pubmed:volume |
481
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
233-43
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:2592494-Animals,
pubmed-meshheading:2592494-Carboxypeptidase B,
pubmed-meshheading:2592494-Carboxypeptidases,
pubmed-meshheading:2592494-Carboxypeptidases A,
pubmed-meshheading:2592494-Chromatography, DEAE-Cellulose,
pubmed-meshheading:2592494-Chromatography, High Pressure Liquid,
pubmed-meshheading:2592494-Electrophoresis, Polyacrylamide Gel,
pubmed-meshheading:2592494-Enzyme Precursors,
pubmed-meshheading:2592494-Humans,
pubmed-meshheading:2592494-Isoelectric Focusing,
pubmed-meshheading:2592494-Multienzyme Complexes,
pubmed-meshheading:2592494-Pancreas,
pubmed-meshheading:2592494-Swine
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pubmed:year |
1989
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pubmed:articleTitle |
The separation of pancreatic procarboxypeptidases by high-performance liquid chromatography and chromatofocusing.
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pubmed:affiliation |
Departament de Bioquímica i Biología Molecular, Universitat Autònoma de Barcelona, Spain.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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