利用实验室信息管理系统管理大分子晶体学数据。

IF 2.6 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Edward Daniel, Rik K Wierenga, Lari Lehtiö
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引用次数: 0

摘要

蛋白质晶体学是一种研究大分子及其复合物原子结构的成熟方法。成功测定结构的先决条件是获得衍射质量的晶体,这可能需要对蛋白质和条件进行大量优化,因此项目可能持续很长时间,并涉及多个用户。从结晶和晶体处理到沉积和出版的工作流程非常明确,因此电子实验室信息管理系统(LIMS)非常适合数据管理。项目的完成需要所有步骤的关键信息,这些信息也应按照 FAIR 原则提供。由于结晶样品通常在不同设施之间运输,LIMS 系统需要捕捉的一个关键功能是在原实验室的结晶设施和同步加速器设施等之间交换元数据。结晶完成后,结构将存入蛋白质数据库(PDB),LIMS 可将 PDB 代码纳入其数据库,从而完成从结晶到结构存入和出版的监管链。专为大分子晶体学设计的 LIMS,IceBear,既可独立安装,也可作为托管服务使用,本文将以 IceBear 中元数据捕获关键功能的实施为例进行讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Managing macromolecular crystallographic data with a laboratory information management system.

Protein crystallography is an established method to study the atomic structures of macromolecules and their complexes. A prerequisite for successful structure determination is diffraction-quality crystals, which may require extensive optimization of both the protein and the conditions, and hence projects can stretch over an extended period, with multiple users being involved. The workflow from crystallization and crystal treatment to deposition and publication is well defined, and therefore an electronic laboratory information management system (LIMS) is well suited to management of the data. Completion of the project requires key information on all the steps being available and this information should also be made available according to the FAIR principles. As crystallized samples are typically shipped between facilities, a key feature to be captured in the LIMS is the exchange of metadata between the crystallization facility of the home laboratory and, for example, synchrotron facilities. On completion, structures are deposited in the Protein Data Bank (PDB) and the LIMS can include the PDB code in its database, completing the chain of custody from crystallization to structure deposition and publication. A LIMS designed for macromolecular crystallography, IceBear, is available as a standalone installation and as a hosted service, and the implementation of key features for the capture of metadata in IceBear is discussed as an example.

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来源期刊
Acta Crystallographica. Section D, Structural Biology
Acta Crystallographica. Section D, Structural Biology BIOCHEMICAL RESEARCH METHODSBIOCHEMISTRY &-BIOCHEMISTRY & MOLECULAR BIOLOGY
CiteScore
4.50
自引率
13.60%
发文量
216
期刊介绍: Acta Crystallographica Section D welcomes the submission of articles covering any aspect of structural biology, with a particular emphasis on the structures of biological macromolecules or the methods used to determine them. Reports on new structures of biological importance may address the smallest macromolecules to the largest complex molecular machines. These structures may have been determined using any structural biology technique including crystallography, NMR, cryoEM and/or other techniques. The key criterion is that such articles must present significant new insights into biological, chemical or medical sciences. The inclusion of complementary data that support the conclusions drawn from the structural studies (such as binding studies, mass spectrometry, enzyme assays, or analysis of mutants or other modified forms of biological macromolecule) is encouraged. Methods articles may include new approaches to any aspect of biological structure determination or structure analysis but will only be accepted where they focus on new methods that are demonstrated to be of general applicability and importance to structural biology. Articles describing particularly difficult problems in structural biology are also welcomed, if the analysis would provide useful insights to others facing similar problems.
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