Literature DB >> 17116480

Oligosaccharide microarrays to map interactions of carbohydrates in biological systems.

Jose L de Paz1, Tim Horlacher, Peter H Seeberger.   

Abstract

Carbohydrate microarrays are becoming a standard tool for glycobiologists to screen large numbers of sugars and elucidate the role of carbohydrates in biological systems. This article describes detailed methods to prepare and use microarrays containing synthetic oligosaccharides as well as a summary of the biological information that can be obtained by using this technology. These methods use different linking chemistries to immobilize a wide range of synthetic oligosaccharides onto glass slides through the formation of a covalent bond. Therefore, this technology enables the elaborate study of a great variety of carbohydrate interactions.

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Year:  2006        PMID: 17116480     DOI: 10.1016/S0076-6879(06)15017-X

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  12 in total

1.  Characterization of annexin A1 glycan binding reveals binding to highly sulfated glycans with preference for highly sulfated heparan sulfate and heparin.

Authors:  T Horlacher; C Noti; J L de Paz; P Bindschädler; M-L Hecht; D F Smith; M N Fukuda; P H Seeberger
Journal:  Biochemistry       Date:  2011-03-03       Impact factor: 3.162

2.  Heparan Sulfate Microarray Reveals That Heparan Sulfate-Protein Binding Exhibits Different Ligand Requirements.

Authors:  Chengli Zong; Andre Venot; Xiuru Li; Weigang Lu; Wenyuan Xiao; Jo-Setti L Wilkes; Catherina L Salanga; Tracy M Handel; Lianchun Wang; Margreet A Wolfert; Geert-Jan Boons
Journal:  J Am Chem Soc       Date:  2017-07-07       Impact factor: 15.419

3.  Bioorthogonal chemical reporter methodology for visualization, isolation and analysis of glycoconjugates.

Authors:  Geert-Jan Boons
Journal:  Carbohydr Chem       Date:  2010

4.  Defining the Interaction of Human Soluble Lectin ZG16p and Mycobacterial Phosphatidylinositol Mannosides.

Authors:  Shinya Hanashima; Sebastian Götze; Yan Liu; Akemi Ikeda; Kyoko Kojima-Aikawa; Naoyuki Taniguchi; Daniel Varón Silva; Ten Feizi; Peter H Seeberger; Yoshiki Yamaguchi
Journal:  Chembiochem       Date:  2015-06-11       Impact factor: 3.164

5.  Profiling heparin-chemokine interactions using synthetic tools.

Authors:  Jose L de Paz; E Ashley Moseman; Christian Noti; Laura Polito; Ulrich H von Andrian; Peter H Seeberger
Journal:  ACS Chem Biol       Date:  2007-11-20       Impact factor: 5.100

Review 6.  Lectins as tools in glycoconjugate research.

Authors:  Albert M Wu; Elwira Lisowska; Maria Duk; Zhangung Yang
Journal:  Glycoconj J       Date:  2009-11       Impact factor: 2.916

7.  Preparation of homogenous oligosaccharide chains from glycosphingolipids.

Authors:  Yu-Teh Li; Chau-Wen Chou; Su-Chen Li; Utaro Kobayashi; Yo-hey Ishibashi; Makoto Ito
Journal:  Glycoconj J       Date:  2009-11       Impact factor: 2.916

8.  Carbohydrate cluster microarrays fabricated on three-dimensional dendrimeric platforms for functional glycomics exploration.

Authors:  Xichun Zhou; Craig Turchi; Denong Wang
Journal:  J Proteome Res       Date:  2009-11       Impact factor: 4.466

9.  Modular synthesis of N-glycans and arrays for the hetero-ligand binding analysis of HIV antibodies.

Authors:  Sachin S Shivatare; Shih-Huang Chang; Tsung-I Tsai; Susan Yu Tseng; Vidya S Shivatare; Yih-Shyan Lin; Yang-Yu Cheng; Chien-Tai Ren; Chang-Chun David Lee; Sujeet Pawar; Charng-Sheng Tsai; Hao-Wei Shih; Yi-Fang Zeng; Chi-Hui Liang; Peter D Kwong; Dennis R Burton; Chung-Yi Wu; Chi-Huey Wong
Journal:  Nat Chem       Date:  2016-03-07       Impact factor: 24.427

10.  Chemo-enzymatic synthesis of poly-N-acetyllactosamine (poly-LacNAc) structures and their characterization for CGL2-galectin-mediated binding of ECM glycoproteins to biomaterial surfaces.

Authors:  Birgit Sauerzapfe; Karel Krenek; Judith Schmiedel; Warren W Wakarchuk; Helena Pelantová; Vladimir Kren; Lothar Elling
Journal:  Glycoconj J       Date:  2008-08-29       Impact factor: 2.916

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