# A comprehensive method of isolating proteins from serum, cerebrospinal fluid, and hippocampal neurons in rats for proteomic profiling using the LC-MS/MS platform

**Authors:** Pratibha Sharma, Rajinder K. Dhamija

PMC · DOI: 10.1016/j.bbrep.2025.102113 · Biochemistry and Biophysics Reports · 2025-06-25

## TL;DR

This paper introduces a streamlined method to isolate proteins from serum, cerebrospinal fluid, and hippocampal neurons in rats for proteomic studies, aiding in neurological disorder research.

## Contribution

A unified, efficient, and reproducible method for isolating proteins from multiple sources in a single animal for downstream proteomic analysis.

## Key findings

- The method enables high-throughput proteomic profiling with small sample volumes.
- It is suitable for isolating proteins from serum, CSF, and hippocampal neurons simultaneously.
- The approach is cost-effective, easy to use, and reproducible.

## Abstract

Neurology research largely utilizes rat brains due to their structural and functional similarities to humans, making them valuable models for studying various neurological conditions. There is growing interest in investigating diseases such as Alzheimer's disease (AD), Parkinson's disease (PD), cognition, and other mental health-related disorders. This has created a need for a comprehensive, combined, and easy-to-follow method to isolate serum, cerebrospinal fluid (CSF), and hippocampal neurons. The hippocampus, responsible for learning and memory, is affected by various neurological and psychiatric disorders. However, obtaining samples like CSF and hippocampal neurons is challenging, especially from small animals like rats. Currently, there is no efficient method for isolating these samples altogether from a single animal, and its use in downstream applications has not been thoroughly tested. We have developed a comprehensive and streamlined method for isolating serum, CSF, and hippocampal neurons from a single animal, suitable for downstream applications such as proteomics and biomarker research. This method involves using high-speed centrifugation instruments and density gradient centrifugation, which are easy to follow. The isolated proteins were identified through mass spectrometry. Our method has been successfully tested for high-throughput applications with small sample volumes, demonstrating its clinical utility. With our simplified approach, proteins in serum, CSF, and neural cells can be studied simultaneously. The method achieves ease of use, cost-effectiveness, and reproducibility, thereby facilitating a better understanding of neurological disorders.

•Cerebrospinal fluid, serum, and brain hippocampal tissue neurons carry important molecules for diagnosis.•A single method can help ease molecule isolation with better coverage.•Proteomics can be useful in identifying diagnostic biomarkers and understanding disease mechanisms.•CSF & hippocampus hold key diagnostic molecules; a unified isolation method can aid biomarker discovery & disease understanding.

Cerebrospinal fluid, serum, and brain hippocampal tissue neurons carry important molecules for diagnosis.

A single method can help ease molecule isolation with better coverage.

Proteomics can be useful in identifying diagnostic biomarkers and understanding disease mechanisms.

CSF & hippocampus hold key diagnostic molecules; a unified isolation method can aid biomarker discovery & disease understanding.

## Linked entities

- **Diseases:** Alzheimer's disease (MONDO:0004975), Parkinson's disease (MONDO:0005180)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Diseases:** neurological (MESH:D009461), neurological and psychiatric disorders (MESH:D001523), PD (MESH:D010300), AD (MESH:D000544)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12264605/full.md

## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12264605/full.md

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Source: https://tomesphere.com/paper/PMC12264605