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iFLinkC-X:一种可扩展框架,用于组装具有可变长度和氨基酸组成的定制基因编码共聚接头。

iFLinkC-X: A Scalable Framework to Assemble Bespoke Genetically Encoded Co-polymeric Linkers of Variable Lengths and Amino Acid Composition.

作者信息

Gräwe Alexander, Merkx Maarten, Stein Viktor

机构信息

Department of Biology, TU Darmstadt, 64287 Darmstadt, Germany.

Centre for Synthetic Biology, TU Darmstadt, 64283 Darmstadt, Germany.

出版信息

Bioconjug Chem. 2022 Jul 20;33(7):1415-1421. doi: 10.1021/acs.bioconjchem.2c00250. Epub 2022 Jul 11.

Abstract

Linker engineering is rapidly gaining prominence as protein engineers and synthetic biologists construct increasingly sophisticated protein assemblies capable of executing complex molecular functions in the context of biosensing, biocatalysis, or biotherapeutics. Depending on the application, the structural and functional requirements imposed on the underlying linkers can differ vastly. At the same time, there is a distinct lack of methods to effectively code linkers at the level of DNA and tailor them to the functional requirements of different fusion proteins. Addressing these limitations, a scalable framework is presented to compose co-polymeric linkers of variable lengths and amino acid composition based on a limited number of linker fragments stored in sequence-verified entry plasmids. The assembly process is exemplified for Pro-rich linkers in the context of a Zn-responsive dual-readout BRET/FRET sensor while examining how linker composition impacts key functional properties such as ligand affinity, dynamic range, and their ability to separate structurally distinct domains.

摘要

随着蛋白质工程师和合成生物学家构建出越来越复杂的蛋白质组装体,这些组装体能够在生物传感、生物催化或生物治疗的背景下执行复杂的分子功能,接头工程正迅速崭露头角。根据应用的不同,对接头的结构和功能要求可能会有很大差异。与此同时,明显缺乏在DNA水平上有效编码接头并使其适应不同融合蛋白功能要求的方法。为了解决这些限制,本文提出了一个可扩展的框架,用于基于存储在经序列验证的入门质粒中的有限数量的接头片段,构建可变长度和氨基酸组成的共聚接头。在锌响应双读出BRET/FRET传感器的背景下,以富含脯氨酸的接头为例说明了组装过程,同时研究接头组成如何影响关键功能特性,如配体亲和力、动态范围以及它们分离结构不同结构域的能力。

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