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利用特异性单克隆抗体开发用于检测酸噬酸菌(Aac)的表面等离子体共振成像技术。

Development of surface plasmon resonance imaging for detection of Acidovorax avenae subsp. citrulli (Aac) using specific monoclonal antibody.

机构信息

Center of Intelligent Materials and Systems, Nanotec Center of Excellence at Mahidol University, Bangkok 10400, Thailand.

出版信息

Biosens Bioelectron. 2011 Jan 15;26(5):2341-6. doi: 10.1016/j.bios.2010.10.007. Epub 2010 Oct 14.

DOI:10.1016/j.bios.2010.10.007
PMID:21093249
Abstract

An immunosensor based on surface plasmon resonance imaging (SPR imaging) using a specific monoclonal antibody 11E5 (MAb 11E5) was developed for the detection of the seed-borne bacterium Acidovorax avenae subsp. citrulli (Aac), which causes fruit blotch in watermelons and cantaloupes, and compared to the conventional ELISA technique. The 1:40 mixed self-assembled monolayer (mixed SAM) surface was used for the immobilized MAb 11E5 on sensor surface for the detection of Aac. Both whole cells and broken cells of Aac were tested by using direct and sandwich detection assay. The limit of detection (LOD) of Aac using the SPR imaging technique and a direct detection assay was 10(6)cfu/ml and a subsequent amplification of the SPR signal using a polyclonal antibody (PAb) lowered the LOD to 5×10(5) cfu/ml. The LOD for the ELISA technique was 5×10(4) cfu/ml for the detection of Aac, which was slightly better than that for the SPR technique. However, the sensor surface based on SPR imaging offered a major advantage in terms of surface regeneration, allowing at least five cycles with a shorter time assay, multi-channel analysis with an application on multiplex detection, and an ease of the surface usage for the detection of Aac in the naturally infected plant. The surface was tested against the naturally infected sample and showed good selectivity toward the Aac bacteria.

摘要

基于表面等离子体共振成像(SPR 成像)的免疫传感器使用特异性单克隆抗体 11E5(MAb 11E5)开发,用于检测种子携带的细菌酸噬细胞亚种。西瓜和哈密瓜的果实斑点,与传统的 ELISA 技术相比。1:40 混合自组装单层(混合 SAM)表面用于固定化 MAb 11E5在传感器表面用于检测 Aac。使用直接和夹心检测法测试了 Aac 的整个细胞和破碎细胞。使用 SPR 成像技术和直接检测法检测 Aac 的检测限(LOD)为 10(6)cfu/ml,随后使用多克隆抗体(PAb)放大 SPR 信号将 LOD 降低至 5×10(5)cfu/ml。用于检测 Aac 的 ELISA 技术的 LOD 为 5×10(4)cfu/ml,略优于 SPR 技术。然而,基于 SPR 成像的传感器表面在表面再生方面具有主要优势,允许至少五个循环具有较短的时间测定,多通道分析具有多重检测的应用,以及易于使用表面检测自然感染植物中的 Aac。该表面针对自然感染的样本进行了测试,对 Aac 细菌表现出良好的选择性。

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