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蛋白质错误折叠与聚集。

Protein misfolding and aggregation.

作者信息

Murphy Regina M, Kendrick Brent S

机构信息

Department of Chemical and Biological Engineering, University of Wisconsin, Madison, Wisconsin 53706, USA.

出版信息

Biotechnol Prog. 2007 May-Jun;23(3):548-52. doi: 10.1021/bp060374h. Epub 2007 Apr 11.

Abstract

Interest in the problem of protein misfolding and aggregation has exploded in recent years for two reasons: (1) the sharp rise in the number and volume of therapeutic proteins produced commercially and (2) the recognition of the central role of protein aggregates in degenerative diseases. The systematic study of protein aggregation presents major challenges to both the experimentalist and the theoretician. Much of the work retains an empirical flavor due to the experimental complexities; the sensitivity of protein aggregation to the slightest change in protein amino acid composition, solvent properties, or protein concentration; and the lack of robust theoretical models of misfolding and aggregation. Novel experimental and computational approaches are being developed, and we anticipate substantial progress will be made in the near future. Several presentations describing the latest advances in protein misfolding and aggregation were given at the American Chemical Society meeting (BIOT division) held in September, 2006 in San Francisco.

摘要

近年来,对蛋白质错误折叠和聚集问题的关注激增,原因有二:(1)商业生产的治疗性蛋白质数量和规模急剧增加;(2)认识到蛋白质聚集体在退行性疾病中的核心作用。蛋白质聚集的系统研究给实验人员和理论学家都带来了重大挑战。由于实验的复杂性、蛋白质聚集对蛋白质氨基酸组成、溶剂性质或蛋白质浓度的最微小变化的敏感性以及缺乏关于错误折叠和聚集的强大理论模型,许多工作仍带有经验性。新的实验和计算方法正在开发中,我们预计在不久的将来会取得重大进展。在2006年9月于旧金山举行的美国化学学会会议(BIOT分会)上,有几场报告介绍了蛋白质错误折叠和聚集的最新进展。

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