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[一种新的指导理论:信息从多肽序列逆向流向RNA的可能性,特别是在抗体合成中,以及耐受性诱导和免疫抑制的机制(作者译)]

[A new instruction theory: possibility of a reverse flow of information from polypeptide sequences to RNA particularly in antibody synthesis, and the mechanisms of tolerance induction and immunosuppression (author's transl)].

作者信息

Theurer K

出版信息

Infection. 1975;3(3):178-82. doi: 10.1007/BF01641347.

Abstract

A new instruction theory for antibody formation is presented. The reverse flow of information from the amino-acid sequences of small antigenic determinants to an antideterminant RNA (aRNA) seems feasible. Prerequisites are specific activating enzymes, tRNAs, ATP as well as some kind of membrane assembling the anticodons of tRNAs linearly, analogous to the linear primary structure of stretched polypeptides. Once synthesized, aRNA might be replicated, utilized as transfer factor and transcribed by means of Reverse Transcriptase into aDNA. Further steps would be the fusion of this aDNA with genetical performed DNA-molecules already coding for the basic strucures of different classes of immunoglobulins by means of a terminal deoxynucleotidyl-transferase. This could be a chromosomal or extrachromosomal integration. The second hypothesis concerns antigen-induced immunosuppression and the phenomenon of nonresponsiveness (tolerance). An overwhelming proteolysis might give rise to a degradation of antigens or receptor templates for antigenic determinants located on the surface of macrophages. On later exposure to a similar antigen proteolytic enzymes are already preformed abolishing rapidly antigenic information. The third hypothesis concerns antibody-induced immunosuppression and tolerance. Antideterminant information is integrated into the genome or established extra-chromosomally. The continuous presence of antibodies sets in motion a sequence of reactions causing an accumulation of all information intermediates including a complementary DNA strand to the aRNA. On exposure to the corresponding antigen aRNA is transcribed. However, translation might be inhibited by hybridisation with the complementary aDNA strand as well as specific RNA hydrolysis by RNase H. Concerning the immunogenity of antibodies, a proteolytical mechanism might also be possible. Taking this into account a tolerance could be suspended in the following way: 1. by influencing the overwhelming proteolytical degradation of antigenic determinants with simultaneous antigenic stimulation; 2. by substitution of aRNA to induce blocked antibody synthesis.

摘要

本文提出了一种新的抗体形成指导理论。从小抗原决定簇的氨基酸序列到抗决定簇RNA(aRNA)的信息逆向流动似乎是可行的。其先决条件是特定的激活酶、转运RNA(tRNA)、三磷酸腺苷(ATP)以及某种能将tRNA的反密码子线性组装的膜结构,这类似于伸展多肽的线性一级结构。一旦合成,aRNA可能会被复制,用作转移因子,并通过逆转录酶转录成互补DNA(aDNA)。进一步的步骤将是通过末端脱氧核苷酸转移酶,使这种aDNA与已经编码不同类免疫球蛋白基本结构的遗传DNA分子融合。这可能是一种染色体或染色体外整合。第二个假说是关于抗原诱导的免疫抑制和无反应性(耐受性)现象。过度的蛋白水解可能导致抗原或巨噬细胞表面抗原决定簇的受体模板降解。在随后接触类似抗原时,蛋白水解酶已预先形成,会迅速消除抗原信息。第三个假说是关于抗体诱导的免疫抑制和耐受性。抗决定簇信息被整合到基因组中或在染色体外建立。抗体的持续存在引发一系列反应,导致所有信息中间体积累,包括与aRNA互补的DNA链。在接触相应抗原时,aRNA被转录。然而,翻译可能会因与互补aDNA链杂交以及核糖核酸酶H(RNase H)对特定RNA的水解而受到抑制。关于抗体的免疫原性,蛋白水解机制也有可能。考虑到这一点,耐受性可以通过以下方式解除:1. 通过在抗原刺激的同时影响抗原决定簇的过度蛋白水解降解;2. 通过替换aRNA来诱导被阻断的抗体合成。

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