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Intrinsically Disordered Proteins: An Update Keynote Paper of IEEE 7th BIBE, Oct. 14-17 Harvard Medical School Conference Center

机译:本质无序的蛋白质:10月14日至17月14日至17点到17年的IEEE第7个BIBE的更新主题纸

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Just over 10 years ago, in June, 1997, in the Proceedings of the IEEE International Conference on Neural Networks, we published our first predictor of intrinsically disordered protein [1]. Since then, we have substantially improved our predictors, andmore than 20 other laboratory groups have joined in efforts to improve the prediction of protein disorder. At the algorithmic level, prediction of protein intrinsic disorder is similar to the prediction of secondary structure, but, at the structural level, secondary structure and intrinsic disorder are entirely different. The secondary structure class called random coil or irregular differs from intrinsic disorder due to very different dynamic properties, with the secondary structure class being much less mobile than the region of disorder. At the biological level, unlike the prediction of secondary structure, the prediction of intrinsic disorder has been revolutionary. That is, for many years, experimentalists have provided evidence that some proteins lack fixed structure or are disordered (or unfolded) under physiological conditions. Experimentalists further are showing that, for some proteins, functions depended on the unstructured rather than structured state. However, these examples have been mostly ignored. To our knowledge, not one disordered protein or disorder-associated function is discussed in any biochemistry textbook, even though such examples began to be discovered more than 50 years ago. Disorder prediction has been important for showing that the few experimentally characterized examples represent a very large cohort that is found all across all three domains of life. We now know that many significant biological functions depend directly on, or are importantly associated with, the unfolded or partially folded state. In this paper, we will briefly review some of the key discoveries that have occurred in the last decade, and, furthermore, will make a few highly speculative projections.
机译:在1997年6月,在1997年6月,在IEEE的神经网络国际会议的诉讼程序中,我们发表了本质无序蛋白质的第一个预测因子[1]。从那时起,我们大大改善了我们的预测因素,而且除20的其他实验室组已经加入努力改善蛋白质障碍的预测。在算法水平,蛋白质内在病症的预测类似于二级结构的预测,但是,在结构水平,二次结构和内在病症完全不同。由于具有非常不同的动态性质,所谓的随机线圈或不规则不同的二级结构类与内在病症不同,二级结构类比无序区域更少。在生物学层面,与二级结构的预测不同,内在疾病的预测一直是革命性的。也就是说,多年来,实验主义者提供了证据表明,一些蛋白质在生理条件下缺乏固定结构或在生理条件下紊乱(或展开)。实验主义者进一步表明,对于一些蛋白质,功能依赖于非结构化而不是结构化状态。但是,这些例子主要被忽略了。为了我们的知识,在任何生物化学教科书中都讨论了任何无序的蛋白质或无序相关的功能,即使这些例子在50年以上开始被发现。疾病预测对于表明少数实验表征的例子表示很重要,这是一个非常大的群组,这些群体在所有三个生命领域中发现。我们现在知道许多重要的生物学功能直接依赖,或者与展开或部分折叠的状态相关联。在本文中,我们将简要审查过去十年中发生的一些主要发现,而且还将制造一些高度投机性的预测。

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