Chemical Lectinology: Tools for Probing the Ligands and Dynamics of Mammalian Lectins In Vivo

被引:22
作者
Belardi, Brian [1 ,2 ]
Bertozzi, Carolyn R. [3 ,4 ]
机构
[1] Univ Calif Berkeley, Dept Chem & Mol & Cell Biol, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Howard Hughes Med Inst, Berkeley, CA 94720 USA
[3] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[4] Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA
来源
CHEMISTRY & BIOLOGY | 2015年 / 22卷 / 08期
关键词
GLCNAC-MODIFIED PROTEINS; C-TYPE LECTIN; SYNTHETIC GLYCOPROTEIN MIMICS; RESONANCE ENERGY-TRANSFER; PHOTO-CROSS-LINKING; L-SELECTIN; SIALIC-ACID; DEVELOPING ZEBRAFISH; SIGNAL-TRANSDUCTION; ENDOTHELIAL-CELLS;
D O I
10.1016/j.chembiol.2015.07.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The importance and complexity associated with the totality of glycan structures, i.e. the glycome, has garnered significant attention from chemists and biologists alike. However, what is lacking from this biochemical picture is how cells, tissues, and organisms interpret glycan patterns and translate this information into appropriate responses. Lectins, glycan-binding proteins, are thought to bridge this gap by decoding the glycome and dictating cell fate based on the underlying chemical identities and properties of the glycome. Yet, our understanding of the in vivo ligands and function for most lectins is still incomplete. This review focuses on recent advances in chemical tools to study the specificity and dynamics of mammalian lectins in live cells. A picture emerges of lectin function that is highly sensitive to its organization, which in turn drastically shapes immunity and cancer progression. We hope this review will inspire biologists to make use of these new techniques and stimulate chemists to continue developing innovative approaches to probe lectin biology in vivo.
引用
收藏
页码:983 / 993
页数:11
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