Approaches toward High‐Mannose‐Type Glycan Libraries |
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| Authors: | Kohki Fujikawa Akira Seko Yoichi Takeda Yukishige Ito |
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| Affiliation: | 1. Japan Science and Technology Agency (JST), ERATO Ito Glycotrilogy Project, Wako, Saitama, Japan;2. SUNTORY Bioorganic Research Institute, Seika‐cho Soraku‐gun, Kyoto, Japan;3. Department of Biotechnology, College of Life Sciences, Ritsumeikan University, Kusatsu, Shiga, Japan;4. Synthetic Cellular Chemistry Laboratory, RIKEN, Wako, Saitama, Japan |
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| Abstract: | Asparagine‐linked (N‐linked) sugar chains are widely found in the rough endoplasmic reticulum (ER), which has attracted renewed attention because of its participation in the glycoprotein quality control process. In the ER, newly formed glycoproteins are properly folded to higher‐order structures by the action of a variety of lectin chaperones and processing enzymes and are transported into the Golgi, while terminally misfolded glycoproteins are carried into the cytosol for degradation. A group of proteins related to this system are known to recognize subtle differences in the high‐mannose‐type oligosaccharide structures of glycoproteins; however, their molecular foundations are still unclear. In order to gain a more precise understanding, our group has established a strategy for the systematic synthesis of high‐mannose‐type glycans. More recently, we have developed “top‐down” chemoenzymatic approaches that allow expeditious access to theoretically all types of high‐mannose glycans. This strategy comprehensively delivered 37 high‐mannose‐type glycans, including G1M9–M3 glycans, and opened up the possibility of the elucidation of structure–function relationships with a series of high‐mannose‐type glycans. |
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| Keywords: | carbohydrates glycoconjugates glycoproteins glycosylation protein folding |
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