Literature DB >> 3123427

Enzyme binding to detect carbohydrate expression in tissue sections. 1. Native and cross-linked glucose oxidase.

A Leathem1, S Brooks.   

Abstract

Enzymes may be useful as highly specific histochemical probes to identify and localize macromolecular substrates in tissue sections. We have used glucose oxidase, a double-headed enzyme, to demonstrate beta-glucosyl groups in paraffin sections. Native glucose oxidase has two active sites per molecule. Soluble polymers formed by glutaraldehyde combine many active binding sites on to one molecule. Some of these bind to glucose in tissue sections, leaving others free to react with chromogenic substrate. The intensity of staining is directly related to the concentration of enzyme, duration of incubation with enzyme, temperature and pH. Polymeric forms of enzyme are about 100 times more effective than native. Glucose oxidase, particularly in a polymeric form, appears a simple reagent for the identification of glucose-containing structures. The use of native and polymerized enzymes as a histochemical probe has enormous potential in the analysis of normal tissues and in the detection of aberrant carbohydrate deposition in pathological tissues; this system serves as a useful model.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3123427     DOI: 10.1007/bf01675750

Source DB:  PubMed          Journal:  Histochem J        ISSN: 0018-2214


  12 in total

1.  Purification, properties, and molecular features of glucose oxidase from Aspergillus niger.

Authors:  H Tsuge; O Natsuaki; K Ohashi
Journal:  J Biochem       Date:  1975-10       Impact factor: 3.387

2.  Enzymic activity and conformational properties of native and crosslinked glucose oxidase.

Authors:  B Solomon; N Lotan; E Katchalski-Katzir
Journal:  Biopolymers       Date:  1977-09       Impact factor: 2.505

3.  New structural model of E. coli aspartate transcarbamylase and the amino-acid sequence of the regulatory polypeptide chain.

Authors:  K Weber
Journal:  Nature       Date:  1968-06-22       Impact factor: 49.962

4.  Allosteric interactions in aspartate transcarbamylase. I. Binding of specific ligands to the native enzyme and its isolated subunits.

Authors:  J P Changeux; J C Gerhart; H K Schachman
Journal:  Biochemistry       Date:  1968-02       Impact factor: 3.162

5.  Subunit structure of glucose oxidase from Aspergillus niger.

Authors:  J J O'Malley; J L Weaver
Journal:  Biochemistry       Date:  1972-09-12       Impact factor: 3.162

6.  The pH dependence of the individual steps in the glucose oxidase reaction.

Authors:  H J Bright; M Appleby
Journal:  J Biol Chem       Date:  1969-07-10       Impact factor: 5.157

Review 7.  Methods in ultrastructural cytochemistry of the cell nucleus.

Authors:  G Moyne
Journal:  Prog Histochem Cytochem       Date:  1980

8.  Multiple forms of glucose oxidase with different carbohydrate compositions.

Authors:  S Hayashi; S Nakamura
Journal:  Biochim Biophys Acta       Date:  1981-01-15

9.  The dissociation of glucose oxidase by sodium n-dodecyl sulphate.

Authors:  M N Jones; P Manley; A Wilkinson
Journal:  Biochem J       Date:  1982-04-01       Impact factor: 3.857

10.  Cytochemical detection of mannose-specific receptors for glycoproteins with horseradish peroxidase as a ligand.

Authors:  W Straus
Journal:  Histochemistry       Date:  1981
View more
  1 in total

Review 1.  Development of glucose-responsive 'smart' insulin systems.

Authors:  Nischay K Rege; Nelson F B Phillips; Michael A Weiss
Journal:  Curr Opin Endocrinol Diabetes Obes       Date:  2017-08       Impact factor: 3.243

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.