Nilsen B M, Grimsøen A, Paulsen B S
Institute of Pharmacy, University of Oslo, Blindern, Norway.
Mol Immunol. 1991 Jul;28(7):733-42. doi: 10.1016/0161-5890(91)90116-2.
Mugwort (Artemisia vulgaris L.) pollen allergens, separated by SDS-PAGE or IEF, were identified after transfer to NCM by incubation with a panel of sera from 16 patients with clinical mugwort pollen allergy, followed by [125I]anti-IgE and autoradiography. Of the at least 23 components separated by SDS-PAGE in a 15% polyacrylamide gel, at least 15 components with mol. wts 12,000-100,000 bound IgE from the panel of patient sera. A component of mol. wt 22,000 bound IgE from at least 94% of the patient sera tested and for all but three sera this component also bound the greatest quantity of IgE. Five other components with mol. wts 12,000, 17,000, 29,000, 39,000 and 42,000 bound IgE from 75-94% of the patient sera. After separation by IEF, at least 28 protein bands were detected in the pI region 3.5-7.2 and at least seven bands were found in the region 8.6-9.3. At least 11 bands in the pI range 4.2-7.3 and at least five bands in the pI region 8.5-9.2 bound IgE from the panel of patient sera. The most intense radiostaining was observed with a component having a pI of 4.35, which bound IgE from 31% of the patient sera. Immunoblotting of the SDS-PAGE and IEF gels using specific rabbit antisera and human sera against three important mugwort pollen allergens, denoted Ag 9, Ag 12 and Ag 13, was performed to determine the mol. wt and pI of these allergens which had earlier only been identified in CIE/CRIE. The results revealed that Ag 13 had a mol. wt of 61,000 and a pI of 4.35, Ag 12 had a mol. wt of 22,000 and AG 9 had pIs in the region 4.55-5.55 (six isoforms). Ag 9 did not bind IgE after SDS-PAGE and was thus not identified in the SDS-PAGE pattern, and Ag 12 failed to be detected in the NCM after transfer from IEF gels. By crossed immunoelectrofocusing, Ag 12 was found to consist of several isoforms predominantly located in the pI region 3.5-5.1. The immunoblotting analysis also revealed that the glycoprotein allergen Art v II was not detected after transfer from either SDS-PAGE or IEF gels. In conclusion, immunoblotting analysis of SDS-PAGE and IEF gels are useful methods for characterization of mugwort pollen extract, but it should be noted that some important allergens which are easily identified in CIE/CRIE may fail to be detected by these methods.
用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)或等电聚焦电泳(IEF)分离的艾蒿(Artemisia vulgaris L.)花粉过敏原,在转移至硝酸纤维素膜(NCM)后,与16例临床诊断为艾蒿花粉过敏患者的一组血清进行温育,然后用[125I]抗IgE和放射自显影法进行鉴定。在15%聚丙烯酰胺凝胶中通过SDS-PAGE分离出的至少23种成分中,至少有15种分子量在12,000至100,000之间的成分与患者血清组中的IgE结合。一种分子量为22,000的成分与至少94%检测的患者血清中的IgE结合,除三份血清外,对于所有其他血清,该成分也结合了最大量的IgE。其他五种分子量分别为12,000、17,000、29,000、39,000和42,000的成分与75%至94%的患者血清中的IgE结合。通过IEF分离后,在pH值3.5至7.2区域检测到至少28条蛋白带,在8.6至9.3区域发现至少7条带。在pH值范围4.2至7.3中至少11条带以及在pH值区域8.5至9.2中至少5条带与患者血清组中的IgE结合。观察到pH值为4.35的一种成分放射染色最强,它与31%的患者血清中的IgE结合。使用针对三种重要艾蒿花粉过敏原(分别标记为Ag 9、Ag 12和Ag 13)的特异性兔抗血清和人血清对SDS-PAGE和IEF凝胶进行免疫印迹分析,以确定这些过敏原的分子量和pH值,这些过敏原此前仅在免疫双扩散/交叉免疫电泳(CIE/CRIE)中被鉴定。结果显示,Ag 13的分子量为61,000,pH值为4.35,Ag 12的分子量为22,000,Ag 9的pH值在4.55至5.55区域(六种同工型)。Ag 9在SDS-PAGE后不结合IgE,因此在SDS-PAGE图谱中未被鉴定出来,并且从IEF凝胶转移至NCM后未检测到Ag 12。通过交叉免疫电聚焦发现,Ag 12由几种主要位于pH值3.5至5.1区域的同工型组成。免疫印迹分析还显示,从SDS-PAGE或IEF凝胶转移后均未检测到糖蛋白过敏原Art v II。总之,SDS-PAGE和IEF凝胶的免疫印迹分析是鉴定艾蒿花粉提取物的有用方法,但应注意,一些在CIE/CRIE中易于鉴定的重要过敏原可能无法通过这些方法检测到。