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轴突再生的多组学分析中的规范性概念。

Concept of Normativity in Multi-Omics Analysis of Axon Regeneration.

机构信息

Miami Integrative Metabolomics Research Center, Bascom Palmer Eye Institute, University of Miami, Miami, FL 33136, USA.

Graduate Program in Molecular Cellular Pharmacology, University of Miami, Miami, FL 33136, USA.

出版信息

Biomolecules. 2024 Jun 21;14(7):735. doi: 10.3390/biom14070735.

Abstract

Transcriptomes and proteomes can be normalized with a handful of RNAs or proteins (or their peptides), such as GAPDH, β-actin, RPBMS, and/or GAP43. Even with hundreds of standards, normalization cannot be achieved across different molecular mass ranges for small molecules, such as lipids and metabolites, due to the non-linearity of mass by charge ratio for even the smallest part of the spectrum. We define the amount (or range of amounts) of metabolites and/or lipids per a defined amount of a protein, consistently identified in all samples of a multiple-model organism comparison, as the normative level of that metabolite or lipid. The defined protein amount (or range) is a normalized value for one cohort of complete samples for which intrasample relative protein quantification is available. For example, the amount of citrate (a metabolite) per µg of aconitate hydratase (normalized protein amount) identified in the proteome is the normative level of citrate with aconitase. We define normativity as the amount of metabolites (or amount range) detected when compared to normalized protein levels. We use axon regeneration as an example to illustrate the need for advanced approaches to the normalization of proteins. Comparison across different pharmacologically induced axon regeneration mouse models entails the comparison of axon regeneration, studied at different time points in several models designed using different agents. For the normalization of the proteins across different pharmacologically induced models, we perform peptide doping (fixed amounts of known peptides) in each sample to normalize the proteome across the samples. We develop Regen V peptides, divided into Regen III (SEB, LLO, CFP) and II (HH4B, A1315), for pre- and post-extraction comparisons, performed with the addition of defined, digested peptides (bovine serum albumin tryptic digest) for protein abundance normalization beyond commercial labeled relative quantification (for example, 18-plex tandem mass tags). We also illustrate the concept of normativity by using this normalization technique on regenerative metabolome/lipidome profiles. As normalized protein amounts are different in different biological states (control versus axon regeneration), normative metabolite or lipid amounts are expected to be different for specific biological states. These concepts and standardization approaches are important for the integration of different datasets across different models of axon regeneration.

摘要

转录组和蛋白质组可以用少量 RNA 或蛋白质(或其肽段)进行标准化,如 GAPDH、β-肌动蛋白、RPBMS 和/或 GAP43。即使使用数百种标准品,也无法实现小分子(如脂质和代谢物)在不同分子量范围内的归一化,因为即使是光谱中最小的部分,质荷比也不是线性的。我们将每个定义量(或定义量范围)的蛋白质中代谢物和/或脂质的量(或范围)定义为多模式生物体比较中所有样本中一致鉴定的、该代谢物或脂质的规范水平。定义的蛋白质量(或范围)是一组完整样本的归一化值,对于这些样本,有内部样本相对蛋白质定量。例如,在蛋白质组中鉴定出的乌头酸水合酶(归一化蛋白量)每 µg 的柠檬酸量(代谢物量)是乌头酸酶的柠檬酸规范水平。我们将规范性定义为与归一化蛋白水平相比检测到的代谢物(或量范围)的量。我们以轴突再生为例来说明需要采用先进方法对蛋白质进行归一化。在不同的药理学诱导的轴突再生小鼠模型之间进行比较,需要比较在几个使用不同试剂设计的模型中不同时间点研究的轴突再生。为了在不同的药理学诱导模型之间对蛋白质进行归一化,我们在每个样本中进行肽掺杂(已知肽的固定量),以在样本之间对蛋白质组进行归一化。我们开发了 Regen V 肽,分为 Regen III(SEB、LLO、CFP)和 II(HH4B、A1315),用于预提取和后提取比较,方法是添加定义的、消化的肽(牛血清白蛋白胰蛋白酶消化物)进行蛋白质丰度归一化,超越商业标记相对定量(例如,18 重串联质量标签)。我们还通过使用这种归一化技术对再生代谢组/脂质组图谱进行说明,说明了规范性的概念。由于在不同的生物学状态(对照与轴突再生)下,归一化蛋白量不同,因此特定生物学状态下的规范代谢物或脂质量预计会有所不同。这些概念和标准化方法对于整合不同的轴突再生模型数据集非常重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b8c/11274927/f13ab70b0687/biomolecules-14-00735-g001.jpg

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