» Articles » PMID: 28002079

Unbiased and Targeted Mass Spectrometry for the HDL Proteome

Overview
Specialty Biochemistry
Date 2016 Dec 22
PMID 28002079
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose Of Review: Mass spectrometry is an ever evolving technology that is equipped with a variety of tools for protein research. Some lipoprotein studies, especially those pertaining to HDL biology, have been exploiting the versatility of mass spectrometry to understand HDL function through its proteome. Despite the role of mass spectrometry in advancing research as a whole, however, the technology remains obscure to those without hands on experience, but still wishing to understand it. In this review, we walk the reader through the coevolution of common mass spectrometry workflows and HDL research, starting from the basic unbiased mass spectrometry methods used to profile the HDL proteome to the most recent targeted methods that have enabled an unprecedented view of HDL metabolism.

Recent Findings: Unbiased global proteomics have demonstrated that the HDL proteome is organized into subgroups across the HDL size fractions providing further evidence that HDL functional heterogeneity is in part governed by its varying protein constituents. Parallel reaction monitoring, a novel targeted mass spectrometry method, was used to monitor the metabolism of HDL apolipoproteins in humans and revealed that apolipoproteins contained within the same HDL size fraction exhibit diverse metabolic properties.

Summary: Mass spectrometry provides a variety of tools and strategies to facilitate understanding, through its proteins, the complex biology of HDL.

Citing Articles

Clot or Not? Reviewing the Reciprocal Regulation Between Lipids and Blood Clotting.

Zhang Z, Rodriguez M, Zheng Z Arterioscler Thromb Vasc Biol. 2024; 44(3):533-544.

PMID: 38235555 PMC: 10922732. DOI: 10.1161/ATVBAHA.123.318286.


Understanding HDL Metabolism and Biology Through In Vivo Tracer Kinetics.

Andraski A, Sacks F, Aikawa M, Singh S Arterioscler Thromb Vasc Biol. 2023; 44(1):76-88.

PMID: 38031838 PMC: 10842918. DOI: 10.1161/ATVBAHA.123.319742.


Mass Spectrometry-Based Approaches for Clinical Biomarker Discovery in Traumatic Brain Injury.

Creech M, Carvalho L, McCoy H, Jacobs J, Hinson H Curr Treat Options Neurol. 2023; 24(12):605-618.

PMID: 37025501 PMC: 10072855. DOI: 10.1007/s11940-022-00742-3.


Lipoprotein proteome profile: novel insight into hyperlipidemia.

Lin M, Li M, Zheng H, Sun H, Zhang J Clin Transl Med. 2021; 11(4):e361.

PMID: 33931962 PMC: 8032137. DOI: 10.1002/ctm2.361.


Metabolism of PLTP, CETP, and LCAT on multiple HDL sizes using the Orbitrap Fusion Lumos.

Singh S, Andraski A, Higashi H, Ho Lee L, Ramsaroop A, Sacks F JCI Insight. 2020; 6(3).

PMID: 33351780 PMC: 7934878. DOI: 10.1172/jci.insight.143526.


References
1.
Lee H, Kang U, Moon H, Lee J, Lee K, Yi M . Development and Validation of a Novel Plasma Protein Signature for Breast Cancer Diagnosis by Using Multiple Reaction Monitoring-based Mass Spectrometry. Anticancer Res. 2015; 35(11):6271-9. View

2.
Gafvels M, Bengtson P . A fast semi-quantitative LC-MS method for measurement of intact apolipoprotein A-I reveals novel proteoforms in serum. Clin Chim Acta. 2015; 442:87-95. DOI: 10.1016/j.cca.2015.01.011. View

3.
Lassman M, McAvoy T, Lee A, Chappell D, Wong O, Zhou H . Practical immunoaffinity-enrichment LC-MS for measuring protein kinetics of low-abundance proteins. Clin Chem. 2014; 60(9):1217-24. PMC: 4955776. DOI: 10.1373/clinchem.2014.222455. View

4.
Pendharkar N, Gajbhiye A, Taunk K, RoyChoudhury S, Dhali S, Seal S . Quantitative tissue proteomic investigation of invasive ductal carcinoma of breast with luminal B HER2 positive and HER2 enriched subtypes towards potential diagnostic and therapeutic biomarkers. J Proteomics. 2015; 132:112-30. DOI: 10.1016/j.jprot.2015.11.024. View

5.
Mendivil C, Furtado J, Morton A, Wang L, Sacks F . Novel Pathways of Apolipoprotein A-I Metabolism in High-Density Lipoprotein of Different Sizes in Humans. Arterioscler Thromb Vasc Biol. 2015; 36(1):156-65. PMC: 4690755. DOI: 10.1161/ATVBAHA.115.306138. View