生物晶体学:过去,现在,未来。

Hfsp Journal Pub Date : 2010-06-01 Epub Date: 2010-04-22 DOI:10.2976/1.3369281
Richard Giegé, Claude Sauter
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引用次数: 19

摘要

生物结晶学从先驱时代到当今全球生物学时代的演变,与过去60年来分子样品制备和结构阐明的方法学和仪器学进展有关。强调了该领域的跨学科性,这产生了物理学和生物学主题之间的交叉融合。特别是,讨论了绕过生物结晶学主要瓶颈的策略。它们涉及(i)大分子靶标的选择、设计和表征方式,(ii)晶体发生以及如何处理影响结晶生长和优化晶体的物理和生物参数,以及(iii)晶体分析和3D结构测定的方法。生物结晶学史上的里程碑事件说明了这一讨论。最后,展望了该领域的未来。需要填补结构空间的大缺口,膜蛋白以及本质上非结构化的蛋白仍然是具有挑战性的靶标。解决日益复杂的超分子组装,开发“4D生物学”来解密大分子结构的运动变化,将这些结构数据整合到整个细胞组织中,并破译生物医学意义,将代表新的前沿。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Biocrystallography: past, present, future.

The evolution of biocrystallography from the pioneers' time to the present era of global biology is presented in relation to the development of methodological and instrumental advances for molecular sample preparation and structure elucidation over the last 6 decades. The interdisciplinarity of the field that generated cross-fertilization between physics- and biology-focused themes is emphasized. In particular, strategies to circumvent the main bottlenecks of biocrystallography are discussed. They concern (i) the way macromolecular targets are selected, designed, and characterized, (ii) crystallogenesis and how to deal with physical and biological parameters that impact crystallization for growing and optimizing crystals, and (iii) the methods for crystal analysis and 3D structure determination. Milestones that have marked the history of biocrystallography illustrate the discussion. Finally, the future of the field is envisaged. Wide gaps of the structural space need to be filed and membrane proteins as well as intrinsically unstructured proteins still constitute challenging targets. Solving supramolecular assemblies of increasing complexity, developing a "4D biology" for decrypting the kinematic changes in macromolecular structures in action, integrating these structural data in the whole cell organization, and deciphering biomedical implications will represent the new frontiers.

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Hfsp Journal
Hfsp Journal 综合性期刊-综合性期刊
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