A barcode-specific immobilization interface for microfluidics-assisted uniform spatially barcoded microarray analysis.

IF 3.3 3区 化学 Q2 CHEMISTRY, ANALYTICAL
Analyst Pub Date : 2025-09-10 DOI:10.1039/d5an00534e
Sidi Tian, Yingxue Li, Jia Yao, Changxiang Huan, Wei Zhang, Shuli Li, Zhiqi Zhang, Zhen Guo, Qi Yang, Chao Li, Chuanyu Li, Jinze Li, Lianqun Zhou
{"title":"A barcode-specific immobilization interface for microfluidics-assisted uniform spatially barcoded microarray analysis.","authors":"Sidi Tian, Yingxue Li, Jia Yao, Changxiang Huan, Wei Zhang, Shuli Li, Zhiqi Zhang, Zhen Guo, Qi Yang, Chao Li, Chuanyu Li, Jinze Li, Lianqun Zhou","doi":"10.1039/d5an00534e","DOIUrl":null,"url":null,"abstract":"<p><p>Microfluidics-assisted spatially barcoded microarray technology offers a high-throughput, low-cost approach towards spatial transcriptomic profiling. A uniform barcoded microarray is crucial for spatially unbiased mRNA analysis. However, non-specific adsorption of barcoding reagents in microchannels occurs during liquid transport, causing non-uniform barcoding in the chip's functional regions. The uneven microarray further leads to biased transcriptome capture. Herein, we develop a barcode-specific immobilization (BarSI) interface with both anti-adsorption properties and biological activity for the development of uniform spatially barcoded microarray chips. We immobilize DNA probes in straight and serpentine microchannels with coefficients of variation (CV) of 2.3% and 3.2%. Based on the orthogonal barcoding system, we developed spatially barcoded microarray chips with an overall fluorescence intensity CV of 8.47 ± 1.26%, compared with the CV of 20.91 ± 2.84% of microarrays developed on conventional amino glass slides. Using the uniform spatially barcoded microarray chip, we achieved spatially unbiased detection of mouse liver mRNA with an absolute value of Moran's <i>I</i> below 0.05. We present an economical and accessible method for manufacturing uniform spatially barcoded microarray chips, introducing a novel strategy for unbiased transcriptome analysis.</p>","PeriodicalId":63,"journal":{"name":"Analyst","volume":" ","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2025-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analyst","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5an00534e","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Microfluidics-assisted spatially barcoded microarray technology offers a high-throughput, low-cost approach towards spatial transcriptomic profiling. A uniform barcoded microarray is crucial for spatially unbiased mRNA analysis. However, non-specific adsorption of barcoding reagents in microchannels occurs during liquid transport, causing non-uniform barcoding in the chip's functional regions. The uneven microarray further leads to biased transcriptome capture. Herein, we develop a barcode-specific immobilization (BarSI) interface with both anti-adsorption properties and biological activity for the development of uniform spatially barcoded microarray chips. We immobilize DNA probes in straight and serpentine microchannels with coefficients of variation (CV) of 2.3% and 3.2%. Based on the orthogonal barcoding system, we developed spatially barcoded microarray chips with an overall fluorescence intensity CV of 8.47 ± 1.26%, compared with the CV of 20.91 ± 2.84% of microarrays developed on conventional amino glass slides. Using the uniform spatially barcoded microarray chip, we achieved spatially unbiased detection of mouse liver mRNA with an absolute value of Moran's I below 0.05. We present an economical and accessible method for manufacturing uniform spatially barcoded microarray chips, introducing a novel strategy for unbiased transcriptome analysis.

用于微流体辅助均匀空间条形码微阵列分析的条形码特定固定界面。
微流体辅助的空间条形码微阵列技术为空间转录组分析提供了一种高通量、低成本的方法。统一的条形码微阵列对于空间无偏mRNA分析至关重要。然而,在液体运输过程中,条形码试剂在微通道中发生非特异性吸附,导致芯片功能区域的条形码不均匀。不均匀的微阵列进一步导致转录组捕获的偏差。在此,我们开发了一种具有抗吸附性能和生物活性的条形码特异性固定化(BarSI)接口,用于开发均匀空间条形码微阵列芯片。我们将DNA探针固定在直线型和蛇形微通道中,变异系数(CV)分别为2.3%和3.2%。基于正交条形码系统,我们开发了空间条形码微阵列芯片,其整体荧光强度CV为8.47±1.26%,而传统氨基玻璃载玻片微阵列的CV为20.91±2.84%。利用均匀空间条形码微阵列芯片,我们实现了小鼠肝脏mRNA的空间无偏检测,Moran's I绝对值小于0.05。我们提出了一种经济可行的方法来制造均匀的空间条形码微阵列芯片,引入了一种无偏倚转录组分析的新策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Analyst
Analyst 化学-分析化学
CiteScore
7.80
自引率
4.80%
发文量
636
审稿时长
1.9 months
期刊介绍: "Analyst" journal is the home of premier fundamental discoveries, inventions and applications in the analytical and bioanalytical sciences.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信