Terminator: A Software Package for Fast and Local Optimization of His-Tag Placement for Protein Affinity Purification

IF 3.8 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Rokas Gerulskis,  and , Shelley D. Minteer*, 
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引用次数: 0

Abstract

Although the use of affinity tags can greatly improve purification of expressed enzymes, the placement of affinity tags can significantly impact the expression, solubility, and function of recombinant proteins. To facilitate the optimal design of 6xHis-tagged constructs for protein purification, we developed Terminator, a Python-based software package, which takes a UniProt ID or existing protein sequence as input, identifies related sequences, maps sequence conservation retrieved from ConSurf onto protein 3D structures retrieved from the PDB and SWISS-MODEL, and analyzes proximity to cavities and functional sites to recommend the N- or C-terminus for placement of 6xHis fusion tags <15 residues in length. The package also outputs a document with available purification and activity literature for the target and closely related proteins organized by year. Comparative analysis of Terminator predictions against published experimental tag behavior for 6xHis fusion tags <15 residues in length demonstrates an 86–100% accuracy in predicting the relative risk of ill effects between termini and a 92–93% accuracy in predicting the absolute risk of modifying individual termini. This reliability of Terminator’s analysis suggests that proximity to surface cavities, not burial of wild-type termini, is the most reliable predictor of ill effects arising from short 6xHis fusion tags. This tool aims to expedite construct design and enhance the successful production of well-behaved proteins for studies in enzymology and biocatalysis with minimal need for computational resources, programming knowledge, or familiarity with protein-tag interference mechanisms.

Terminator:一个用于蛋白质亲和纯化的快速和局部优化his标签放置的软件包
虽然使用亲和标签可以大大提高表达酶的纯化,但亲和标签的放置会显著影响重组蛋白的表达、溶解度和功能。为了便于6xhis标记构建体的优化设计,我们开发了基于python的软件包Terminator,该软件包以UniProt ID或现有蛋白质序列为输入,识别相关序列,将从ConSurf检索到的序列保守性映射到从PDB和SWISS-MODEL检索到的蛋白质3D结构上。并分析与空腔和功能位点的接近程度,以推荐长度为15个残基的6xHis融合标签的N端或c端位置。该软件包还输出一个文件,其中包含按年组织的目标蛋白和密切相关蛋白的纯化和活性文献。对长度为15个残基的6xHis融合标签的终结者预测与已发表的实验标签行为的比较分析表明,预测末端之间不良反应的相对风险的准确率为86-100%,预测修饰单个末端的绝对风险的准确率为92-93%。终结者分析的可靠性表明,接近表面空腔,而不是埋藏野生型末端,是短6xHis融合标签引起的不良影响的最可靠的预测因素。该工具旨在加快结构设计,提高酶学和生物催化研究中行为良好的蛋白质的成功生产,而对计算资源,编程知识或熟悉蛋白质标签干扰机制的需求最小。
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来源期刊
ACS Bio & Med Chem Au
ACS Bio & Med Chem Au 药物、生物、化学-
CiteScore
4.10
自引率
0.00%
发文量
0
期刊介绍: ACS Bio & Med Chem Au is a broad scope open access journal which publishes short letters comprehensive articles reviews and perspectives in all aspects of biological and medicinal chemistry. Studies providing fundamental insights or describing novel syntheses as well as clinical or other applications-based work are welcomed.This broad scope includes experimental and theoretical studies on the chemical physical mechanistic and/or structural basis of biological or cell function in all domains of life. It encompasses the fields of chemical biology synthetic biology disease biology cell biology agriculture and food natural products research nucleic acid biology neuroscience structural biology and biophysics.The journal publishes studies that pertain to a broad range of medicinal chemistry including compound design and optimization biological evaluation molecular mechanistic understanding of drug delivery and drug delivery systems imaging agents and pharmacology and translational science of both small and large bioactive molecules. Novel computational cheminformatics and structural studies for the identification (or structure-activity relationship analysis) of bioactive molecules ligands and their targets are also welcome. The journal will consider computational studies applying established computational methods but only in combination with novel and original experimental data (e.g. in cases where new compounds have been designed and tested).Also included in the scope of the journal are articles relating to infectious diseases research on pathogens host-pathogen interactions therapeutics diagnostics vaccines drug-delivery systems and other biomedical technology development pertaining to infectious diseases.
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