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无细胞液滴微反应器中的高效多基因表达

Efficient multi-gene expression in cell-free droplet microreactors.

作者信息

Sierra Ana Maria Restrepo, Arold Stefan T, Grünberg Raik

机构信息

Biological and Environmental Science and Engineering Division, King Abdullah University of Science and Technology (KAUST), Thuwal, Kingdom of Saudi Arabia.

KAUST Computational Bioscience Research Center, King Abdullah University of Science and Technology, Thuwal, Kingdom of Saudi Arabia.

出版信息

PLoS One. 2022 Mar 21;17(3):e0260420. doi: 10.1371/journal.pone.0260420. eCollection 2022.

Abstract

Cell-free transcription and translation systems promise to accelerate and simplify the engineering of proteins, biological circuits and metabolic pathways. Their encapsulation on microfluidic platforms can generate millions of cell-free reactions in picoliter volume droplets. However, current methods struggle to create DNA diversity between droplets while also reaching sufficient protein expression levels. In particular, efficient multi-gene expression has remained elusive. We here demonstrate that co-encapsulation of DNA-coated beads with a defined cell-free system allows high protein expression while also supporting genetic diversity between individual droplets. We optimize DNA loading on commercially available microbeads through direct binding as well as through the sequential coupling of up to three genes via a solid-phase Golden Gate assembly or BxB1 integrase-based recombineering. Encapsulation with an off-the-shelf microfluidics device allows for single or multiple protein expression from a single DNA-coated bead per 14 pL droplet. We envision that this approach will help to scale up and parallelize the rapid prototyping of more complex biological systems.

摘要

无细胞转录和翻译系统有望加速并简化蛋白质、生物电路和代谢途径的工程设计。将它们封装在微流控平台上,可以在皮升体积的液滴中产生数百万个无细胞反应。然而,目前的方法在液滴间创造DNA多样性的同时,还难以达到足够的蛋白质表达水平。特别是,高效的多基因表达一直难以实现。我们在此证明,将包被DNA的珠子与特定的无细胞系统共同封装,既能实现高蛋白质表达,又能支持单个液滴间的遗传多样性。我们通过直接结合以及经由基于固相金门组装或基于BxB1整合酶的重组工程对多达三个基因进行顺序偶联,来优化市售微珠上的DNA负载。使用现成的微流控装置进行封装,可在每个14皮升的液滴中从单个包被DNA的珠子实现单蛋白或多蛋白表达。我们设想,这种方法将有助于扩大规模并并行化更复杂生物系统的快速原型制作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0739/8936439/fc1ae7418098/pone.0260420.g001.jpg

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