Globotriose-functionalized gold nanoparticles as multivalent probes for Shiga-like toxin

被引:86
作者
Chien, Yuh-Yih [1 ,2 ,3 ]
Jan, Mi-Dan [4 ]
Adak, Avijit Kumar [4 ]
Tzeng, Hsiao-Chien [5 ]
Lin, Yen-Ping [5 ]
Chen, Yu-Ju [1 ,2 ]
Wang, Ken-Tseng [3 ]
Chen, Chien-Tien [5 ]
Chen, Chia-Chun [5 ]
Lin, Chun-Cheng [1 ,2 ,4 ]
机构
[1] Acad Sinica, Inst Chem, Taipei 128, Taiwan
[2] Acad Sinica, Genom Res Ctr, Taipei 128, Taiwan
[3] Natl Taiwan Univ, Dept Chem, Taipei 106, Taiwan
[4] Natl Tsing Hua Univ, Dept Chem, Hsinchu 300, Taiwan
[5] Natl Taiwan Normal Univ, Dept Chem, Taipei 116, Taiwan
关键词
glycoconjugates; multivalent interaction; P-k antigen; Shiga-like toxin; surface plasmon resonance;
D O I
10.1002/cbic.200700590
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
Compared to monovalent carbohydrates, multivalent carbohydrate ligands exhibit significantly enhanced binding affinities to their interacting proteins. Here, we report globotriose (P-k ligand)-functionalized gold nanoparticle (AuNP) probes for the investigation of multivalent interactions with the B, subunit of Shiga-like toxin I (B-Slt). Six P-k-ligand-encapsuloted AuNPs (P-k-AuNPs) of varying particle size and linker length were synthesized and evaluated for their potential as multivalent offinity probes by using a surface plasmon resonance competition assay. The affinity of these probes for the interacting proteins was greatly affected by nanoparticle size, linker length, and ligand density on nanoparticle surface. For example, the 20-nm 20-P-k-1-AuNP which had a relatively long linker showed a > 10(8)-fold increase in affinity compared with the mono P-k ligand. This intrinsic high-affinity AuNP probe specifically captured the recombinant B-Slt from Escherichia coli lysate, and the resulting purity of the B-Slt was > 95 %. We also developed a robust P-k-AuNP-based detection method for Slt-I by combining the technique with silver enhancement.
引用
收藏
页码:1100 / 1109
页数:10
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