Document Detail


Purification and characterization of a lectin-like substance from silkworm faeces.
MedLine Citation:
PMID:  8242795     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
To obtain biologically active substances that are useful in the study of cell structures and functions, we examined several biological activities of an extract of silkworm faeces with hot buffer. We detected a lectin-like substance in the extract and purified it. When the extract of silkworm faeces was added to a culture of quail myoblasts transformed with temperature-sensitive Rous sarcoma virus (QM-RSV cells), the plated cells which were cultured at 35.5 degrees C (the permissive temperature for RSV that suppresses myogenic differentiation) became detached from the dishes and the cells in suspension aggregated. However, when the same amount of extract was added to plated QM-RSV cells cultured at 41 degrees C, which is a nonpermissive temperature for RSV, the cells did not become detached. Other kinds of plated cells examined also did not become detached. Unlike plated cells, nonplated cells of all kinds aggregate in suspension upon the addition of the extract. This active substance was purified by monitoring its induction of cell aggregation. The purified substance was found to be a lectin-like glycoprotein with an apparent molecular mass of about 60 kDa. Further studies showed that the binding sites of this glycoprotein are sugar chains on the cell surface and that mannose is an epitope.
Authors:
E Hirayama; N Ishikawa; T Yano-Inoue; J Kim
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Cell structure and function     Volume:  18     ISSN:  0386-7196     ISO Abbreviation:  Cell Struct. Funct.     Publication Date:  1993 Jun 
Date Detail:
Created Date:  1994-01-06     Completed Date:  1994-01-06     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  7608465     Medline TA:  Cell Struct Funct     Country:  JAPAN    
Other Details:
Languages:  eng     Pagination:  161-71     Citation Subset:  IM    
Affiliation:
Institute of Molecular and Cellular Biology for Pharmaceutical Sciences, Kyoto Pharmaceutical University, Japan.
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MeSH Terms
Descriptor/Qualifier:
Animals
Bombyx / chemistry*
Cell Aggregation / drug effects
Cell Line, Transformed
Cells, Cultured
Chickens
Feces / chemistry
Glycoproteins / chemistry,  isolation & purification*,  pharmacology
Hela Cells
Humans
Lectins / chemistry,  isolation & purification*,  pharmacology
Male
Mice
Muscles / cytology,  drug effects
Quail
Chemical
Reg. No./Substance:
0/Glycoproteins; 0/Lectins

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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