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蛋白质合成中建模效率、误差传播及误差增强药物的影响

Modelling efficiency, error propagation and the effect of error-enhancing drugs in protein synthesis.

作者信息

Blomberg C

机构信息

Department of Theoretical Physics, Royal Institute of Technology, Stockholm, Sweden.

出版信息

Biomed Biochim Acta. 1990;49(8-9):879-89.

PMID:2082928
Abstract

The efficiency of protein synthesis is discussed with the main emphasis on the accuracy. The error increase by erroneous synthesizing proteins is studied by a theoretical model which includes the coupling of the amino acylation step to the protein synthesis at the ribosomes. Depending on parameter values, the model yields a stable point of relatively high accuracy, a point where most of the accuracy is lost and virtually no functioning proteins are produced (error catastrophe), or both. The effect of an error enhancing drug such as streptomycin can be considered, and it is found that one can have a situation where small amounts of the drug yields a decreased but stable accuracy, and where this possibility disappears at a certain drug level. At higher drug levels, the cells cannot attain any accuracy. The transition is quite drastic, and analogous to a phase transition.

摘要

本文主要围绕蛋白质合成的准确性探讨了其效率。通过一个理论模型研究了错误合成蛋白质导致的错误增加情况,该模型包括氨酰化步骤与核糖体上蛋白质合成的耦合。根据参数值,该模型会产生一个相对高精度的稳定点、一个大部分准确性丧失且几乎不产生功能性蛋白质的点(错误灾难),或者两者皆有。可以考虑诸如链霉素等错误增强药物的影响,结果发现,可能存在这样一种情况:少量药物会使准确性降低但保持稳定,而在一定药物水平下这种可能性会消失。在更高的药物水平下,细胞无法达到任何准确性。这种转变非常剧烈,类似于相变。

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