The Miller Hypothesis.

David A Haake
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Abstract

The immune response is a cornerstone in the body's struggle against microbial pathogens. In ways that we do not yet completely understand, the mammalian immune response has evolved to identify proteins of pathogens that are either important virulence factors or key immunoprotective targets. Professor James N. Miller suggested that one way to discover such proteins is to harness the power of the immune system in the laboratory.This general concept, referred to here as the Miller Hypothesis, took several different manifestations in the discovery of some of the best known and widely studied leptospiral proteins: The porin OmpL1 was identified by surface immunoprecipitation, leptospiral immunoglobulin-like proteins were uncovered by screening a genomic library with sera from leptospirosis patients, and the major outer-membrane lipoprotein LipL32 was recognized through immunoblot studies. Such approaches will continue to bear fruit for both the leptospiral research field and research on other invasive pathogens.

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米勒假说。
免疫反应是人体对抗微生物病原体的基石。哺乳动物的免疫反应已经进化到可以识别病原体的蛋白质,这些蛋白质要么是重要的毒力因子,要么是关键的免疫保护靶点。詹姆斯·n·米勒(James N. Miller)教授建议,发现这种蛋白质的一种方法是在实验室中利用免疫系统的力量。这一普遍概念,在这里被称为米勒假说,在发现一些最著名和被广泛研究的钩端螺旋体蛋白时表现出了几种不同的表现:通过表面免疫沉淀鉴定了孔蛋白OmpL1,通过筛选钩端螺旋体患者血清的基因组文库发现了钩端螺旋体免疫球蛋白样蛋白,通过免疫印迹研究识别了主要的外膜脂蛋白LipL32。这种方法将继续在钩端螺旋体研究领域和其他侵入性病原体的研究中取得成果。
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