Solid-liquid interface method (SLIM): a new crystallization method for proteins.

Solid-liquid interface method (SLIM): a new crystallization method for proteins.
复制标题

DOI:
10.1016/j.bbrc.2009.06.086
复制
发表时间:
2009-09
影响因子:
3.1
通讯作者:
E. Brostromer;J. Nan;Lan-fen Li;X. Su
E. Brostromer;J. Nan;Lan-fen Li;X. Su
中科院分区:
生物学4区
文献类型:
--
作者:
E. Brostromer;J. Nan;Lan-fen Li;X. Su

文献摘要

被引文献

相似文献

尽管理论、方法和技术取得了令人瞩目的进步,但结晶仍然是大分子结构测定的严重瓶颈。在这里,我们提出了一种用于蛋白质结晶的新型固液界面方法(SLIM),该方法基于结晶试剂的预添加和干燥,然后将蛋白质溶液分配到干燥的介质中以启动从固液界面的结晶。该方法不仅快速且易于执行,还允许使用浓度较低的蛋白质溶液来建立结晶试验。
Despite impressive advances in theories, methods and technologies, crystallization still remains a serious bottleneck in structural determination of macromolecules. Here we present a novel solid–liquid interface method (SLIM) for protein crystallization, based on the pre-adding and drying of a crystallization reagent, and thereafter the dispensing of a protein solution to the dried media to initiate crystallization from the solid–liquid interface. Not only quick and easy to perform, the method also allows for a less concentrated protein solution for setting up crystallization trials.