首页> 美国卫生研究院文献>Springer Open Choice >Precise co-registration of mass spectrometry imaging histology and laser microdissection-based omics
【2h】

Precise co-registration of mass spectrometry imaging histology and laser microdissection-based omics

机译:质谱成像组织学和基于激光显微切割的组学的精确共配准

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Mass spectrometry imaging (MSI) is an analytical technique for the unlabeled and multiplex imaging of molecules in biological tissue sections. It therefore enables the spatial and molecular annotations of tissues complementary to histology. It has already been shown that MSI can guide subsequent material isolation technologies such as laser microdissection (LMD) to enable a more in-depth molecular characterization of MSI-highlighted tissue regions. However, with MSI now reaching spatial resolutions at the single-cell scale, there is a need for a precise co-registration between MSI and the LMD. As proof-of-principle, MSI of lipids was performed on a breast cancer tissue followed by a segmentation of the data to detect molecularly distinct segments within its tumor areas. After image processing of the segmentation results, the coordinates of the MSI-detected segments were passed to the LMD system by three co-registration steps. The errors of each co-registration step were quantified and the total error was found to be less than 13 μm. With this link established, MSI data can now accurately guide LMD to excise MSI-defined regions of interest for subsequent extract-based analyses. In our example, the excised tissue material was then subjected to ultrasensitive microproteomics in order to determine predominant molecular mechanisms in each of the MSI-highlighted intratumor segments. This work shows how the strengths of MSI, histology, and extract-based omics can be combined to enable a more comprehensive molecular characterization of in situ biological processes.Electronic supplementary materialThe online version of this article (10.1007/s00216-019-01983-z) contains supplementary material, which is available to authorized users.
机译:质谱成像(MSI)是一种用于生物组织切片中分子的未标记和多重成像的分析技术。因此,它使组织的空间和分子注释与组织学互补。已经表明,MSI可以指导后续的材料隔离技术,例如激光显微切割(LMD),以实现对MSI突出的组织区域的更深入的分子表征。但是,由于MSI现在已达到单小区规模的空间分辨率,因此需要在MSI和LMD之间进行精确的共配准。作为原理证明,对乳腺癌组织进行脂质MSI分析,然后对数据进行分割以检测其肿瘤区域内的分子不同部分。在对分割结果进行图像处理后,通过三个共配准步骤将MSI检测到的片段的坐标传递给LMD系统。量化每个共同注册步骤的误差,发现总误差小于13μm。通过建立此链接,MSI数据现在可以准确地指导LMD切除MSI定义的感兴趣区域,以进行后续的基于提取物的分析。在我们的实例中,然后对切除的组织材料进行超灵敏的蛋白质组学研究,以确定每个MSI标记的肿瘤内片段的主要分子机制。这项工作显示了如何将MSI,组织学和基于提取物的组学的优势相结合,以实现更全面的原位生物过程分子表征。电子补充材料本文的在线版本(10.1007 / s00216-019-01983-z )包含补充材料,授权用户可以使用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号