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Size distribution of Platanus acerifolia allergen 3 (Pla a3) in Shanghai ambient size-resolved particles and its allergenic effects

机译:悬铃木过敏原3(Pla a3)在上海周围大小分辨颗粒中的大小分布及其致敏作用

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Pollen allergy has become a major problem for a considerable and steadily increasing percentage of people worldwide. Allergenic protein, which is contained in subpollens, can be released from pollen and suspended in air to cause allergenic reactions. However, the distribution of the allergenic protein and its relationship with inorganic ions in ambient particles has not been reported. Here, a recombinantPlatanus acerifoliaallergen3 and tandemsix-histidine epitope (His6) fusion protein (rPla a3) was expressed in a prokaryotic system and then purified by affinity chromatography. The allergenicity of both rPla a3 and natural Pla a3 inPlatanuspollen protein extract was assessed by enzyme-linked immunosorbent assay using the sera of rPla a3-sensitized rats. Our results demonstrated that IgE from rPla a3-sensitized rats could be used to quantify the allergenicity of Pla a3 in the releasedPlatanuspollen and identify the mass level of Pla 3 in size-resolved particles. The peak of natural Pla a3 expression was found in the middle of April, and the highest mass level of Pla a3 occurred in ambient particles diameters larger than 7 μm. The mass concentration of Pla a3 in the atmosphere was consistent with that of the total protein variety, which also showed a peak in particles with diameters larger than 7 μm during thePlatanuspollen season. Remarkably, most Pla a3 existed in particulate matters 7 μm, including intactPlatanuspollen, and non-negligible partitions of Pla a3 were detected in particles with diameters less than 7.0 μm. Major ions (Ca2+, NH4+, and SO42−) in ambient particles not only aggravated pollen rupture and content release, but also affected the distribution of Pla 3 in the particles. Allergic disease could be specifically identified by using rPla a3, and there was a short lag between hospital admission for allergic disease and the peak ofPlatanusprotein concentration in spring.
机译:花粉过敏已经成为世界上相当大比例且稳定增长的人口的主要问题。花粉中包含的过敏原蛋白可以从花粉中释放出来并悬浮在空气中,引起过敏反应。然而,尚未报道致敏蛋白的分布及其与周围颗粒中无机离子的关系。在这里,在原核系统中表达了重组的法国梧桐变应原3和坦地美克斯-组氨酸表位(His6)融合蛋白(rPla a3),然后通过亲和层析纯化。通过使用rPla a3致敏大鼠血清的酶联免疫吸附法评估了Platanuspollen蛋白提取物中rPla a3和天然Pla a3的致敏性。我们的结果表明,来自rPla a3致敏大鼠的IgE可用于定量释放的Platanus花粉中Pla a3的致敏性,并确定大小分辨颗粒中Pla 3的质量水平。在4月中旬发现了天然Pla a3表达的峰值,并且Pla a3的最高质量水平发生在直径大于7μm的环境颗粒中。大气中Pla a3的质量浓度与总蛋白的质量浓度一致,在Platanus花粉季节,直径大于7μm的颗粒中也出现峰值。值得注意的是,大多数Pla a3存在于>7μm的颗粒物质中,包括完整的Platanus花粉,并且在直径小于7.0μm的颗粒中检测到Pla a3的不可忽略的分区。环境粒子中的主要离子(Ca2 +,NH4 +和SO42-)不仅加剧了花粉破裂和含量释放,而且还影响了Pla 3在粒子中的分布。通过使用rPla a3可以特异性地识别过敏性疾病,并且从过敏性疾病入院到春季春季Platanusprotein浓度峰值之间的时间间隔短。

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