首页> 外文期刊>Biochimica et biophysica acta: BBA: International journal of biochemistry, biophysics and molecular biololgy. Proteins and Proteomics >Connecting imaging mass spectrometry and magnetic resonance imaging-based anatomical atlases for automated anatomical interpretation and differential analysis
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Connecting imaging mass spectrometry and magnetic resonance imaging-based anatomical atlases for automated anatomical interpretation and differential analysis

机译:连接成像质谱和基于磁共振成像的解剖结构,用于自动解剖解剖解释和差异分析

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Imaging mass spectrometry (IMS) is a molecular imaging technology that can measure thousands of biomolecules concurrently without prior tagging, making it particularly suitable for exploratory research. However, the data size and dimensionality often makes thorough extraction of relevant information impractical. To help guide and accelerate IMS data analysis, we recently developed a framework that integrates IMS measurements with anatomical atlases, opening up opportunities for anatomy-driven exploration of IMS data. One example is the automated anatomical interpretation of ion images, where empirically measured ion distributions are automatically decomposed into their underlying anatomical structures. While offering significant potential, IMS-atlas integration has thus far been restricted to the Allen Mouse Brain Atlas (AMBA) and mouse brain samples. Here, we expand the applicability of this framework by extending towards new animal species and a new set of anatomical atlases retrieved from the Scalable Brain Atlas (SBA). Furthermore, as many SBA atlases are based on magnetic resonance imaging (MRI) data, a new registration pipeline was developed that enables direct non-rigid IMS-to-MRI registration. These developments are demonstrated on protein-focused FTICR IMS measurements from coronal brain sections of a Parkinson's disease (PD) rat model. The measurements are integrated with an MRI-based rat brain atlas from the SBA. The new rat-focused IMSatlas integration is used to perform automated anatomical interpretation and to find differential ions between healthy and diseased tissue. IMS-atlas integration can serve as an important accelerator in IMS data exploration, and with these new developments it can now be applied to a wider variety of animal species and modalities. This article is part of a Special Issue entitled: MALDI Imaging, edited by Dr. Corinna Henkel and Prof. Peter Hoffmann.
机译:成像质谱(IMS)是一种分子成像技术,可以同时测量数千个生物分子而无需现有标记,使其特别适用于探索性研究。但是,数据规模和维度通常会彻底提取相关信息不切实际。为了帮助指导和加速IMS数据分析,我们最近开发了一个框架,将IMS测量与解剖结构集成,开辟了解剖学驱动的IMS数据的机会。一个例子是离子图像的自动解剖解释,其中经验测量的离子分布被自动分解成其底层的解剖结构。在提供重要潜力的同时,IMS-Atlas集成迄今为止仅限于艾伦小鼠脑地图集(AMBA)和小鼠脑样本。在这里,我们通过朝向新动物物种扩展和从可扩展的脑地图集(SBA)检索的一组新的解剖结构集来扩展本框架的适用性。此外,随着许多SBA地图集基于磁共振成像(MRI)数据,开发了一种新的注册管线,使得能够直接非刚性IMS到MRI注册。这些发展在帕金森病(PD)大鼠模型的冠状脑切片中对蛋白质聚焦的FTICR IMS测量进行了证明。测量与来自SBA的MRI的大鼠大脑图集集成。新的大鼠聚焦的IMSATLAS集成用于进行自动解剖解释并在健康和患病组织之间找到差异离子。 IMS-ATLAS集成可以作为IMS数据探索中的重要加速器,并且对于这些新的开发,现在可以应用于更广泛的动物物种和方式。本文是题为:Maldi成像的特殊问题的一部分,由Corinna Henkel博士和Peter Hoffmann教授编辑。

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