Photoactivatable Crosslinking sugars for capturing glycoprotein interactions

被引:142
作者
Tanaka, Yoshihito
Kohler, Jennifer J. [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
关键词
D O I
10.1021/ja7109772
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Carbohydrates are key mediators of cell-cell, cell-virus, and cell-ligand interactions. These interactions are often difficult to study because they are characterized by fast off rates and low affinities. Photoactivatable crosslinking sugars can be used to capture these transient interactions by forming a covalent bond between the carbohydrate and its binding partner. We designed and synthesized 'photo-sugars' that contain diazirine moieties on the N-acyl side chains. We demonstrated that these photo-sugars could be metabolically incorporated onto the surface of living cells. Upon UV irradiation, specific crosslinks were formed between glycoprotein binding partners. Importantly, photo-sugar incorporation competes efficiently with endogenous carbohydrate biosynthesis and is compatible with the sialic acid modifications, such as 9-O-acetylation, that regulate binding events.
引用
收藏
页码:3278 / +
页数:3
相关论文
共 16 条
[1]   Chemical glycobiology [J].
Bertozzi, CR ;
Kiessling, LL .
SCIENCE, 2001, 291 (5512) :2357-2364
[2]   DIAZIRINES .2. SYNTHESIS AND PROPERTIES OF SMALL FUNCTIONALIZED DIAZIRINE MOLECULES - SOME OBSERVATIONS ON REACTION OF A DIAZIRIDINE WITH IODINE-IODIDE ION SYSTEM [J].
CHURCH, RFR ;
WEISS, MJ .
JOURNAL OF ORGANIC CHEMISTRY, 1970, 35 (08) :2465-&
[3]   Homomultimeric complexes of CD22 in B cells revealed by protein-glycan cross-linking [J].
Han, S ;
Collins, BE ;
Bengtson, P ;
Paulson, JC .
NATURE CHEMICAL BIOLOGY, 2005, 1 (02) :93-97
[4]  
KAYSER H, 1992, J BIOL CHEM, V267, P16934
[5]   Functional groups of sialic acids involved in binding to siglecs (sialoadhesins) deduced from interactions with synthetic analogues [J].
Kelm, S ;
Brossmer, R ;
Isecke, R ;
Gross, HJ ;
Strenge, K ;
Schauer, R .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1998, 255 (03) :663-672
[6]   The ligand-binding domain of CD22 is needed for inhibition of the B cell receptor signal, as demonstrated by a novel human CD22-specific inhibitor compound [J].
Kelm, S ;
Gerlach, J ;
Brossmer, R ;
Danzer, CP ;
Nitschke, L .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (09) :1207-1213
[7]   UDP-GlcNAc 2-epimerase: A regulator of cell surface sialylation [J].
Keppler, OT ;
Hinderlich, S ;
Langner, J ;
Schwartz-Albiez, R ;
Reutter, W ;
Pawlita, M .
SCIENCE, 1999, 284 (5418) :1372-1376
[8]   BIOSYNTHETIC MODULATION OF SIALIC ACID-DEPENDENT VIRUS-RECEPTOR INTERACTIONS OF 2 PRIMATE POLYOMA VIRUSES [J].
KEPPLER, OT ;
STEHLING, P ;
HERRMANN, M ;
KAYSER, H ;
GRUNOW, D ;
REUTTER, W ;
PAWLITA, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (03) :1308-1314
[9]   Expanding the diversity of unnatural cell-surface sialic acids [J].
Luchansky, SJ ;
Goon, S ;
Bertozzi, CR .
CHEMBIOCHEM, 2004, 5 (03) :371-374
[10]   Photo-leucine incorporation reveals the target of a cyclodepsipeptide inhibitor of cotranslational translocation [J].
MacKinnon, Andrew L. ;
Garrison, Jennifer L. ;
Hegde, Rarnanujan S. ;
Taunton, Jack .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (47) :14560-+