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通过凝集素结合分析和抗体反应对日本血吸虫成虫、虫卵和尾蚴碳水化合物的特性进行研究。

Characterization of the carbohydrates of Schistosoma japonicum adult worm, egg and cercaria by analysis of lectin binding and antibody reaction.

作者信息

Beisler G K, Nakao M, Matsuda H, Tanaka H

出版信息

Jpn J Exp Med. 1984 Dec;54(6):263-73.

PMID:6085582
Abstract

Binding of the FITC-labeled lectins, Con A, SBA, WGA, DBA, UEA 1 and RCA 120 were examined on various kinds of cross-sections of S. japonicum adult worms and eggs, and on cercaria specimens. The specificity of the lectin bindings was examined by inhibition test with specific carbohydrates or with unlabeled lectins. Furthermore, the locations of lectin binding in schistosomes were compared with those of the antigen-antibody reactions using the fluorescence technique. It was also studied as to whether lectin binding influenced antigen-antibody reactions. Thus it was found that most lectin binding receptors were located at the same sites, where also FITC-labeled antibodies reacted. But antibodies did not inhibit lectin binding on schistosomes, whereas lectins blocked the antigenic sites to weaken the following antibody reactions on microscope slides. Con A did not show a distinguished pattern on schistosomes, although its carbohydrate specificity was confirmed. On the contrary, the WGA reactions were hardly considered to be carbohydrate specific. PNA and SBA receptors, however, were selectively detected in the egg, testes and adult tegument of schistosomes, corresponding to the sites, where also egg antigenicity was observed. But in the gut of adult schistosomes, in which egg antigenicity was not found, lectin binding with PNA, SBA, UEA 1 and DBA did not occur. Gut reacted only with RCA 120 and Con A. The lectin specificity on tegument of adult schistosomes and on cercaria was similar to that found on egg and testes. The result indicated possibilities of satisfactory purification of schistosomal antigens by using such lectins as PNA, SBA and RCA 120, instead of Con A and WGA, to separate more defined antigenic components.

摘要

研究了异硫氰酸荧光素(FITC)标记的凝集素刀豆球蛋白A(Con A)、大豆凝集素(SBA)、小麦胚凝集素(WGA)、荆豆凝集素(DBA)、荆豆凝集素1(UEA 1)和蓖麻凝集素120(RCA 120)与日本血吸虫成虫和虫卵的各种横断面以及尾蚴标本的结合情况。通过用特定碳水化合物或未标记的凝集素进行抑制试验,检测凝集素结合的特异性。此外,利用荧光技术比较了血吸虫中凝集素结合的位置与抗原-抗体反应的位置。还研究了凝集素结合是否影响抗原-抗体反应。结果发现,大多数凝集素结合受体位于与FITC标记抗体反应的相同位点。但是抗体并不抑制血吸虫上的凝集素结合,而凝集素会封闭抗原位点,从而在显微镜载玻片上削弱随后的抗体反应。尽管Con A的碳水化合物特异性得到了证实,但它在血吸虫上并未显示出明显的模式。相反,WGA反应几乎不被认为具有碳水化合物特异性。然而,在血吸虫的虫卵、睾丸和成虫体表中选择性地检测到了花生凝集素(PNA)和SBA受体,这些部位也观察到了虫卵抗原性。但是在未发现虫卵抗原性的成虫血吸虫肠道中,PNA、SBA、UEA 1和DBA的凝集素结合并未发生。肠道仅与RCA 120和Con A发生反应。成虫血吸虫体表和尾蚴上的凝集素特异性与在虫卵和睾丸上发现的相似。结果表明,使用PNA、SBA和RCA 120等凝集素,而不是Con A和WGA,来分离更明确的抗原成分,有可能令人满意地纯化血吸虫抗原。

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