多孔板盖,用于单步汇集 96 个样本,进行基于条形码的高通量测序。

IF 3 4区 医学 Q3 ENGINEERING, BIOMEDICAL
Stéphanie Boder-Pasche, Mustafa Demir, Sarah Heub, Manon Garzuel, Réal Ischer, Daniel Migliozzi, Siegfried Graf, Noa Schmid, H. Baris Atakan, Daria Gudkova, Daniel Alpern, Riccardo Dainese, Bart Deplancke, Gilles Weder
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引用次数: 0

摘要

高通量转录组学在基础生物学和临床方面的应用日益广泛。从生物库和药物库等大量样本中生成的分子数据正在推动新生物标记物和治疗方法的开发。转录组市场以基因表达为重点,利用下一代测序(NGS)的优势,将 RNA 测序(RNA-seq)作为测量生物样本中全基因组基因表达的标准。繁琐的样本制备(包括 RNA 提取、转化为 cDNA 和扩增)阻碍了 RNA-seq 技术的高通量转化。批量 RNA 条形码和测序(BRB-seq)可通过多孔板格式的样品制备解决这一限制。样品复用与提前汇集到单管相结合,减少了试剂消耗和人工操作步骤。我们的技术依赖于智能实验室器皿:由流体特征和用于输送液体的小针组成的汇集盖,适用于标准 96 孔板,可将多孔板中的所有样本同时汇集到一个试管中。使用标准流体管和泵,该系统可在一分钟内一次性回收 90% 以上的液体。通过从铣削聚碳酸酯/钢原型到注塑聚苯乙烯盖子的过渡,展示了盖子的大规模制造。通过直接从标准 96 孔板中汇集 96 个不同的 DNA 条形码,然后在单个样品池中进行处理,汇集盖展示了其在支持基于条形码的高通量测序方面的价值。这一新的汇集技术显示出巨大的潜力,可满足 BRB-seq 工作流程中的中等通量需求,从而解决 RNA-seq 大规模、高成本效益样本制备的难题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Multi-well plate lid for single-step pooling of 96 samples for high-throughput barcode-based sequencing

Multi-well plate lid for single-step pooling of 96 samples for high-throughput barcode-based sequencing

High-throughput transcriptomics is of increasing fundamental biological and clinical interest. The generation of molecular data from large collections of samples, such as biobanks and drug libraries, is boosting the development of new biomarkers and treatments. Focusing on gene expression, the transcriptomic market exploits the benefits of next-generation sequencing (NGS), leveraging RNA sequencing (RNA-seq) as standard for measuring genome-wide gene expression in biological samples. The cumbersome sample preparation, including RNA extraction, conversion to cDNA and amplification, prevents high-throughput translation of RNA-seq technologies. Bulk RNA barcoding and sequencing (BRB-seq) addresses this limitation by enabling sample preparation in multi-well plate format. Sample multiplexing combined with early pooling into a single tube reduces reagents consumption and manual steps. Enabling simultaneous pooling of all samples from the multi-well plate into one tube, our technology relies on smart labware: a pooling lid comprising fluidic features and small pins to transport the liquid, adapted to standard 96-well plates. Operated with standard fluidic tubes and pump, the system enables over 90% recovery of liquid in a single step in less than a minute. Large scale manufacturing of the lid is demonstrated with the transition from a milled polycarbonate/steel prototype into an injection molded polystyrene lid. The pooling lid demonstrated its value in supporting high-throughput barcode-based sequencing by pooling 96 different DNA barcodes directly from a standard 96-well plate, followed by processing within the single sample pool. This new pooling technology shows great potential to address medium throughput needs in the BRB-seq workflow, thereby addressing the challenge of large-scale and cost-efficient sample preparation for RNA-seq.

Graphical abstract

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来源期刊
Biomedical Microdevices
Biomedical Microdevices 工程技术-工程:生物医学
CiteScore
6.90
自引率
3.60%
发文量
32
审稿时长
6 months
期刊介绍: Biomedical Microdevices: BioMEMS and Biomedical Nanotechnology is an interdisciplinary periodical devoted to all aspects of research in the medical diagnostic and therapeutic applications of Micro-Electro-Mechanical Systems (BioMEMS) and nanotechnology for medicine and biology. General subjects of interest include the design, characterization, testing, modeling and clinical validation of microfabricated systems, and their integration on-chip and in larger functional units. The specific interests of the Journal include systems for neural stimulation and recording, bioseparation technologies such as nanofilters and electrophoretic equipment, miniaturized analytic and DNA identification systems, biosensors, and micro/nanotechnologies for cell and tissue research, tissue engineering, cell transplantation, and the controlled release of drugs and biological molecules. Contributions reporting on fundamental and applied investigations of the material science, biochemistry, and physics of biomedical microdevices and nanotechnology are encouraged. A non-exhaustive list of fields of interest includes: nanoparticle synthesis, characterization, and validation of therapeutic or imaging efficacy in animal models; biocompatibility; biochemical modification of microfabricated devices, with reference to non-specific protein adsorption, and the active immobilization and patterning of proteins on micro/nanofabricated surfaces; the dynamics of fluids in micro-and-nano-fabricated channels; the electromechanical and structural response of micro/nanofabricated systems; the interactions of microdevices with cells and tissues, including biocompatibility and biodegradation studies; variations in the characteristics of the systems as a function of the micro/nanofabrication parameters.
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