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What Cyto- and Histochemistry Can Do to Crack the Sugar Code

As letters form the vocabulary of a language, biochemical ‘symbols’ (the building blocks of oligo- and polymers) make writing molecular messages possible. Compared to nucleotides and amino acids, sugars have chemical properties that facilitate to reach an unsurpassed level of oligomer diversity. The...

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Autores principales: Habermann, Felix A., Kaltner, Herbert, Higuero, Alonso M., García Caballero, Gabriel, Ludwig, Anna-Kristin, C. Manning, Joachim, Abad-Rodríguez, José, Gabius, Hans-Joachim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JAPAN SOCIETY OF HISTOCHEMISTRY AND CYTOCHEMISTRY 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116616/
https://www.ncbi.nlm.nih.gov/pubmed/34012175
http://dx.doi.org/10.1267/ahc.21-00017
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author Habermann, Felix A.
Kaltner, Herbert
Higuero, Alonso M.
García Caballero, Gabriel
Ludwig, Anna-Kristin
C. Manning, Joachim
Abad-Rodríguez, José
Gabius, Hans-Joachim
author_facet Habermann, Felix A.
Kaltner, Herbert
Higuero, Alonso M.
García Caballero, Gabriel
Ludwig, Anna-Kristin
C. Manning, Joachim
Abad-Rodríguez, José
Gabius, Hans-Joachim
author_sort Habermann, Felix A.
collection PubMed
description As letters form the vocabulary of a language, biochemical ‘symbols’ (the building blocks of oligo- and polymers) make writing molecular messages possible. Compared to nucleotides and amino acids, sugars have chemical properties that facilitate to reach an unsurpassed level of oligomer diversity. These glycans are a part of the ubiquitous cellular glycoconjugates. Cyto- and histochemically, the glycans’ structural complexity is mapped by glycophenotyping of cells and tissues using receptors (‘readers’, thus called lectins), hereby revealing its dynamic spatiotemporal regulation: these data support the concept of a sugar code. When proceeding from work with plant (haem)agglutinins as such tools to the discovery of endogenous (tissue) lectins, it became clear that a broad panel of biological meanings can indeed be derived from the sugar-based vocabulary (the natural glycome incl. post-synthetic modifications) by glycan-lectin recognition in situ. As consequence, the immunocyto- and histochemical analysis of lectin expression is building a solid basis for the steps toward tracking down functional correlations, for example in processes leading to cell adhesion, apoptosis, autophagy or growth regulation as well as targeted delivery of glycoproteins. Introduction of labeled tissue lectins to glycan profiling assists this endeavor by detecting counterreceptor(s) in situ. Combining these tools and their applications strategically will help to take the trip toward the following long-range aim: to compile a dictionary for the glycan vocabulary that translates each message (oligosaccharide) into its bioresponse(s), that is to crack the sugar code.
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spelling pubmed-81166162021-05-18 What Cyto- and Histochemistry Can Do to Crack the Sugar Code Habermann, Felix A. Kaltner, Herbert Higuero, Alonso M. García Caballero, Gabriel Ludwig, Anna-Kristin C. Manning, Joachim Abad-Rodríguez, José Gabius, Hans-Joachim Acta Histochem Cytochem Review As letters form the vocabulary of a language, biochemical ‘symbols’ (the building blocks of oligo- and polymers) make writing molecular messages possible. Compared to nucleotides and amino acids, sugars have chemical properties that facilitate to reach an unsurpassed level of oligomer diversity. These glycans are a part of the ubiquitous cellular glycoconjugates. Cyto- and histochemically, the glycans’ structural complexity is mapped by glycophenotyping of cells and tissues using receptors (‘readers’, thus called lectins), hereby revealing its dynamic spatiotemporal regulation: these data support the concept of a sugar code. When proceeding from work with plant (haem)agglutinins as such tools to the discovery of endogenous (tissue) lectins, it became clear that a broad panel of biological meanings can indeed be derived from the sugar-based vocabulary (the natural glycome incl. post-synthetic modifications) by glycan-lectin recognition in situ. As consequence, the immunocyto- and histochemical analysis of lectin expression is building a solid basis for the steps toward tracking down functional correlations, for example in processes leading to cell adhesion, apoptosis, autophagy or growth regulation as well as targeted delivery of glycoproteins. Introduction of labeled tissue lectins to glycan profiling assists this endeavor by detecting counterreceptor(s) in situ. Combining these tools and their applications strategically will help to take the trip toward the following long-range aim: to compile a dictionary for the glycan vocabulary that translates each message (oligosaccharide) into its bioresponse(s), that is to crack the sugar code. JAPAN SOCIETY OF HISTOCHEMISTRY AND CYTOCHEMISTRY 2021-04-28 2021-04-17 /pmc/articles/PMC8116616/ /pubmed/34012175 http://dx.doi.org/10.1267/ahc.21-00017 Text en 2021 The Japan Society of Histochemistry and Cytochemistry https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the Creative Commons License (CC-BY-NC), which permits use, distribution and reproduction of the articles in any medium provided that the original work is properly cited and is not used for commercial purposes.
spellingShingle Review
Habermann, Felix A.
Kaltner, Herbert
Higuero, Alonso M.
García Caballero, Gabriel
Ludwig, Anna-Kristin
C. Manning, Joachim
Abad-Rodríguez, José
Gabius, Hans-Joachim
What Cyto- and Histochemistry Can Do to Crack the Sugar Code
title What Cyto- and Histochemistry Can Do to Crack the Sugar Code
title_full What Cyto- and Histochemistry Can Do to Crack the Sugar Code
title_fullStr What Cyto- and Histochemistry Can Do to Crack the Sugar Code
title_full_unstemmed What Cyto- and Histochemistry Can Do to Crack the Sugar Code
title_short What Cyto- and Histochemistry Can Do to Crack the Sugar Code
title_sort what cyto- and histochemistry can do to crack the sugar code
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116616/
https://www.ncbi.nlm.nih.gov/pubmed/34012175
http://dx.doi.org/10.1267/ahc.21-00017
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