Plant Research International, Wageningen, The Netherlands.
PLoS One. 2013 May 30;8(5):e64040. doi: 10.1371/journal.pone.0064040. Print 2013.
The 16 kDa heat shock protein (HSP) is an immuno-dominant antigen, used in diagnosis of infectious Mycobacterium tuberculosis (M.tb.) causing tuberculosis (TB). Its use in serum-based diagnostics is limited, but for the direct identification of M.tb. bacteria in sputum or cultures it may represent a useful tool. Recently, a broad set of twelve 16 kDa specific heavy chain llama antibodies (VHH) has been isolated, and their utility for diagnostic applications was explored.
METHODOLOGY/PRINCIPAL FINDINGS: To identify the epitopes recognized by the nine (randomly selected from a set of twelve 16 kDa specific VHH antibodies) distinct VHH antibodies, 14 overlapping linear epitopes (each 20 amino acid long) were characterized using direct and sandwich ELISA techniques. Seven out of 14 epitopes were recognized by 8 out of 9 VHH antibodies. The two highest affinity binders B-F10 and A-23 were found to bind distinct epitopes. Sandwich ELISA and SPR experiments showed that only B-F10 was suitable as secondary antibody with both B-F10 and A-23 as anchoring antibodies. To explain this behavior, the epitopes were matched to the putative 3D structure model. Electrospray ionization time-of-flight mass spectrometry and size exclusion chromatography were used to determine the higher order conformation. A homodimer model best explained the differential immunological reactivity of A-23 and B-F10 against heat-treated M.tb. lysates.
CONCLUSIONS/SIGNIFICANCE: The concentrations of secreted antigens of M.tb. in sputum are too low for immunological detection and existing kits are only used for identifying M.tb. in cultures. Here we describe how specific combinations of VHH domains could be used to detect the intracellular HSP antigen. Linked to methods of pre-concentrating M.tb. cells prior to lysis, HSP detection may enable the development of protein-based diagnostics of sputum samples and earlier diagnosis of diseases.
16kDa 热休克蛋白(HSP)是一种免疫优势抗原,用于诊断引起结核病(TB)的传染性结核分枝杆菌(M.tb.)。其在血清诊断中的应用受到限制,但对于直接识别痰或培养物中的 M.tb. 细菌,它可能是一种有用的工具。最近,已经分离出一套广泛的十二种 16kDa 特异性重链骆驼抗体(VHH),并探索了它们在诊断应用中的效用。
方法/主要发现:为了鉴定这九种(随机从十二种 16kDa 特异性 VHH 抗体中选择)不同的 VHH 抗体所识别的表位,使用直接和夹心 ELISA 技术对 14 个重叠的线性表位(每个 20 个氨基酸长)进行了特征描述。在 14 个表位中,有 7 个被 9 个 VHH 抗体中的 8 个识别。两个亲和力最高的结合子 B-F10 和 A-23 被发现结合不同的表位。夹心 ELISA 和 SPR 实验表明,只有 B-F10 适合作为二级抗体,而 B-F10 和 A-23 都适合作为锚定抗体。为了解释这种行为,将表位与假定的 3D 结构模型进行匹配。电喷雾电离飞行时间质谱和尺寸排阻色谱用于确定高级构象。同源二聚体模型很好地解释了 A-23 和 B-F10 对热处理的 M.tb. 裂解物的免疫反应性的差异。
结论/意义:痰中 M.tb. 分泌抗原的浓度太低,无法进行免疫学检测,现有的试剂盒仅用于识别培养物中的 M.tb.。在这里,我们描述了如何使用特定的 VHH 结构域组合来检测细胞内 HSP 抗原。与在裂解前浓缩 M.tb. 细胞的方法相结合,HSP 检测可能使基于蛋白质的痰样本诊断和疾病的早期诊断得以发展。