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Electron Microscopic Studies of the Antigen-Antibody Complex

机译:抗原-抗体复合物的电子显微镜研究

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摘要

Electron micrographs of the ferritin antibody (rabbit) and ferritin (horse) complex have been obtained. The high iron content of the ferritin molecule (23 per cent Fe) allows its molecules to be recognized within the particles of precipitate.Three methods of visualizing the molecular distribution have been developed: (a) small particles of the precipitated complex have been dried on to electron microscope grids and either examined directly or first shadowed with metal and then examined, (b) the precipitate has been centrifuged to a plug which was embedded and thin sections cut from it for examination, (c) the bands formed by allowing antibody and antigen to diffuse together in agar gels have been fixed, embedded and sectioned.All methods have yielded pictures of the distribution of the ferritin within the complex which are broadly similar to what might have been expected from a somewhat irregular lattice as pictured in the Marrack-Heidelberger Lattice Theory.The antibody molecules are not clearly defined but appear as a halo of low density enveloping the ferritin clusters. The distance, centre to centre, between the ferritin molecules is variable, but is, on the average, in the range 200–400 Å. This is greater than the ferritin-ferritin contact distance (100 Å) and is thought to mean that the ferritin molecules are bridged by antibody molecules as pictured in the Lattice Theory.The bands produced in the gel-diffusion test contain islands of ferritin-antibody complex. When equivalent concentrations of reagents are used a single band of precipitate is formed. When excess of either antigen or antibody is used multiple bands of precipitate are formed which contain islands of ferritin antibody complex indistinguishable from those formed in the single band at equivalent concentrations, providing direct evidence for the formation of multiple bands from a single antigen.Ferritin-ferritin contacts have been observed within the complex.Under all the conditions of relative concentration of the two components used here, the particles of precipitated complex seem to be superficially covered with antibody which is seen as a halo about 300–400 Å thick around each cluster. This distance may correspond to the length of the antibody molecule which is deduced from other measurements to be about 300 Å.
机译:已获得铁蛋白抗体(兔)和铁蛋白(马)复合物的电子显微照片。铁蛋白分子中高的铁含量(23%Fe)使得其分子在沉淀颗粒中被识别。已开发出三种观察分子分布的方法:(a)将沉淀的复合物的小颗粒干燥到电子显微镜格栅上,或者直接检查,或者先用金属遮盖然后检查,(b)将沉淀物离心到塞子上,将其嵌入并切成薄片以进行检查;(c)通过允许抗体形成的条带和抗原在琼脂凝胶中扩散到一起已经被固定,包埋和切片。所有方法都产生了铁蛋白在复合物中的分布图,这与Marrack- Heidelberger Lattice Theory。抗体分子的定义不明确,但表现为低密度的光环,包裹着铁蛋白簇。铁蛋白分子之间的中心到中心的距离是可变的,但平均范围是200-400Å。这大于铁蛋白-铁蛋白的接触距离(100Å),并且被认为是意味着铁蛋白分子被抗体分子桥接(如晶格理论所示)。在凝胶扩散测试中产生的条带包含铁蛋白-抗体岛。复杂。当使用等效浓度的试剂时,会形成一条单一的沉淀带。当使用过多的抗原或抗体时,会形成多个沉淀带,这些沉淀带中的铁蛋白抗体复合物岛与以相同浓度在单个谱带中形成的岛蛋白没有区别,从而为从单一抗原形成多个谱带提供了直接证据。在复合物中观察到铁蛋白的接触。在此处使用的两种组分的相对浓度的所有条件下,沉淀的复合物颗粒似乎被抗体表面覆盖,每个簇周围的晕圈约300-400Å 。该距离可以对应于抗体分子的长度,该抗体分子的长度从其他测量结果推导出为约300。

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