Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Oligosaccharide Assembly01:24

Oligosaccharide Assembly

3.4K
Protein glycosylation starts in the ER lumen and continues in the Golgi apparatus. Glycosyltransferases catalyze the addition of sugar molecules or glycosylation of proteins. Usually, these enzymes add sugars to the hydroxyl groups of selected serine or threonine residues to form O-linked glycans or the amino groups of asparagine residues to form N-linked glycans. Different positions on the same polypeptide chain can contain differently linked glycans.
Multiple sugar molecules that may or may...
3.4K
Protein Glycosylation01:25

Protein Glycosylation

9.0K
Glycosylation, the most common post-translational modification for proteins, serves diverse functions. Adding sugars to proteins makes the proteins more resistant to proteolytic digestion. Glycosylated proteins can act as markers and receptors to promote cell-cell adhesion. Additionally, they have many essential quality control functions in the cell, such as correct protein folding and facilitating transport of misfolded proteins to the cytosol, which can be degraded.
Glycosylation occurs in...
9.0K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Solid-Phase Glycolipid Synthesis Expedites Liposome Functionalization.

Journal of the American Chemical Society·2026
Same author

Heparin-binding enhances extracellular listeriolysin O activity, overcoming cholesterol inhibition and pH dependence.

Journal of bacteriology·2026
Same author

Total synthesis of the capsular polysaccharide repeating unit towards the development of a glycoconjugate vaccine against <i>Klebsiella pneumoniae</i> ST512.

Beilstein journal of organic chemistry·2026
Same author

3-Deoxy-3-Fluoro Mannuronic Acid Alginates: Stereoselective Automated Synthesis and Conformational Behaviour.

Angewandte Chemie (International ed. in English)·2026
Same author

Synthesis of sialylated human milk oligosaccharides by automated glycan assembly.

Nature communications·2026
Same author

Integrative Approach to Develop and Characterize Antibodies against the Cancer-Associated Antigen Sialyl Lewis A (CA 19-9).

JACS Au·2026
Same journal

Azo compounds as key intermediates in the synthesis of cinnolines. Recent advances.

Organic & biomolecular chemistry·2026
Same journal

Cyclopentannulation toward hydrindane frameworks for the tricyclic core of (±)-rumphellclovane E and (±)-sarinfacetamides A and B.

Organic & biomolecular chemistry·2026
Same journal

Rosamine derivatives of <i>o</i>-aminothiophenol-triacetate (S-APTRA): a new class of selective fluorescent sensors for Zn<sup>2</sup>.

Organic & biomolecular chemistry·2026
Same journal

Sulfonamides: a decade of development in synthetic methods and biological activity studies.

Organic & biomolecular chemistry·2026
Same journal

TBAF-promoted dephenolative transcarbomylation: direct access to substituted carbamates & thiocarbamates.

Organic & biomolecular chemistry·2026
Same journal

Catalytic synthesis of saturated azacycles using transborylation.

Organic & biomolecular chemistry·2026
See all related articles

Related Experiment Video

Updated: Dec 29, 2025

Hierarchical and Programmable One-Pot Oligosaccharide Synthesis
09:56

Hierarchical and Programmable One-Pot Oligosaccharide Synthesis

Published on: September 6, 2019

7.2K

Automated access to well-defined ionic oligosaccharides.

Yuntao Zhu1, Theodore Tyrikos-Ergas2, Kevin Schiefelbein1

  • 1Department of Biomolecular Systems, Max-Planck-Institute of Colloids and Interfaces, Am Mühlenberg 1, 14476 Potsdam, Germany. martina.delbianco@mpikg.mpg.de.

Organic & Biomolecular Chemistry
|February 11, 2020
PubMed
Summary
This summary is machine-generated.

Automated synthesis of novel ionic oligosaccharides using unique monosaccharides enables structural characterization. This research clarifies how charge patterns influence glycan conformation, advancing polysaccharide science.

More Related Videos

High-throughput Synthesis of Carbohydrates and Functionalization of Polyanhydride Nanoparticles
14:37

High-throughput Synthesis of Carbohydrates and Functionalization of Polyanhydride Nanoparticles

Published on: July 6, 2012

11.8K
Chemo-enzymatic Synthesis of N-glycans for Array Development and HIV Antibody Profiling
11:08

Chemo-enzymatic Synthesis of N-glycans for Array Development and HIV Antibody Profiling

Published on: February 5, 2018

9.1K

Related Experiment Videos

Last Updated: Dec 29, 2025

Hierarchical and Programmable One-Pot Oligosaccharide Synthesis
09:56

Hierarchical and Programmable One-Pot Oligosaccharide Synthesis

Published on: September 6, 2019

7.2K
High-throughput Synthesis of Carbohydrates and Functionalization of Polyanhydride Nanoparticles
14:37

High-throughput Synthesis of Carbohydrates and Functionalization of Polyanhydride Nanoparticles

Published on: July 6, 2012

11.8K
Chemo-enzymatic Synthesis of N-glycans for Array Development and HIV Antibody Profiling
11:08

Chemo-enzymatic Synthesis of N-glycans for Array Development and HIV Antibody Profiling

Published on: February 5, 2018

9.1K

Area of Science:

  • Carbohydrate Chemistry
  • Glycobiology
  • Polymer Science

Background:

  • Ionic polysaccharides play crucial roles in biological processes.
  • Structural characterization of these molecules is hindered by difficult purification and synthesis.
  • Understanding their structure is key to elucidating their biological functions.

Purpose of the Study:

  • To develop an automated synthesis method for ionic oligosaccharides.
  • To characterize the structure of synthesized ionic oligosaccharides.
  • To investigate the impact of charge patterns on glycan conformation.

Main Methods:

  • Automated synthesis utilizing four unique, non-natural monosaccharides.
  • Advanced structural analysis techniques to determine oligosaccharide architecture.
  • Conformational analysis to correlate charge distribution with molecular shape.

Main Results:

  • Successful automated synthesis of a diverse library of ionic oligosaccharides.
  • Detailed structural elucidation of the synthesized compounds.
  • Demonstrated correlation between ionic charge patterns and distinct glycan conformations.

Conclusions:

  • Automated synthesis offers a viable route to structurally complex ionic polysaccharides.
  • Charge distribution is a critical determinant of ionic glycan conformation.
  • This work provides a foundation for designing functional ionic glycans.