Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Proteomics01:33

Proteomics

A proteome is the entire set of proteins that a cell type produces. We can study proteomes using the knowledge of genomes because genes code for mRNAs, and the mRNAs encode proteins. Although mRNA analysis is a step in the right direction, not all mRNAs are translated into proteins.
Proteomics is the study of proteomes' function. It involves the large-scale systematic study of the proteome to denote the protein complement expressed by a genome. Scientist Mark Wilkins coined the term proteomics...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Spontaneous Isomerization of Tau is Most Prevalent in Alzheimer's Disease.

NeuroMarkers·2026
Same author

A Critical Perspective on the Role of Thirdhand Smoke in Tumorigenesis: Initiator or Promoter.

Environment & health (Washington, D.C.)·2026
Same author

Identifying predictive hematological biomarkers for radiation exposure by machine learning in mouse models.

Communications medicine·2026
Same author

Revisiting resonance-excitation collision-induced dissociation for data-independent acquisition.

bioRxiv : the preprint server for biology·2026
Same author

ToxBase: A Multidimensional ToxCast Reference Database for High-Throughput Human Exposome Analysis.

Environmental science & technology·2026
Same author

Prioritizing peptides for targeted mass spectrometry experiments using deep learning.

bioRxiv : the preprint server for biology·2026
Same journal

A human-specific genetic modifier reconfigures large-scale cortical network dynamics underlying behavioral performance.

bioRxiv : the preprint server for biology·2026
Same journal

<i>Staphylococcus aureus</i> uses a eukaryotic-like uridyltransferase to make UDP-GlcNAc for cell wall synthesis.

bioRxiv : the preprint server for biology·2026
Same journal

Dynamic redistribution of eIF4F controls cap-dependent translation initiation.

bioRxiv : the preprint server for biology·2026
Same journal

When does additional information improve accuracy of RNA secondary structure prediction?

bioRxiv : the preprint server for biology·2026
Same journal

Normative brain-state trajectories reveal deviation from healthy aging in Alzheimer's disease.

bioRxiv : the preprint server for biology·2026
Same journal

Noradrenergic infraslow rhythm during sleep is the critical link between heart-rate dynamics and memory consolidation.

bioRxiv : the preprint server for biology·2026
See all related articles

Related Experiment Video

Updated: May 7, 2026

Selected Reaction Monitoring Mass Spectrometry for Absolute Protein Quantification
09:04

Selected Reaction Monitoring Mass Spectrometry for Absolute Protein Quantification

Published on: August 17, 2015

17.7K

Is Protein Quantification and Physical Normalization Always Necessary in Proteomics?

Alex Zelter1, Michael Riffle1, Gennifer E Merrihew1

  • 1Department of Genome Sciences, University of Washington, Seattle, WA, 98195, USA.

Biorxiv : the Preprint Server for Biology
|February 23, 2026
PubMed
Summary
This summary is machine-generated.

Protein quantification is often considered essential for liquid chromatography-mass spectrometry/mass spectrometry (LC-MS/MS) proteomics. This study demonstrates that omitting physical normalization can save time and costs without significantly impacting results after computational normalization.

Keywords:
BCAMass spectrometrynormalizationproteinproteomicsquantitative

More Related Videos

Deep Proteome Profiling by Isobaric Labeling, Extensive Liquid Chromatography, Mass Spectrometry, and Software-assisted Quantification
10:37

Deep Proteome Profiling by Isobaric Labeling, Extensive Liquid Chromatography, Mass Spectrometry, and Software-assisted Quantification

Published on: November 15, 2017

12.8K
Robust Comparison of Protein Levels Across Tissues and Throughout Development Using Standardized Quantitative Western Blotting
08:13

Robust Comparison of Protein Levels Across Tissues and Throughout Development Using Standardized Quantitative Western Blotting

Published on: April 9, 2019

14.9K

Related Experiment Videos

Last Updated: May 7, 2026

Selected Reaction Monitoring Mass Spectrometry for Absolute Protein Quantification
09:04

Selected Reaction Monitoring Mass Spectrometry for Absolute Protein Quantification

Published on: August 17, 2015

17.7K
Deep Proteome Profiling by Isobaric Labeling, Extensive Liquid Chromatography, Mass Spectrometry, and Software-assisted Quantification
10:37

Deep Proteome Profiling by Isobaric Labeling, Extensive Liquid Chromatography, Mass Spectrometry, and Software-assisted Quantification

Published on: November 15, 2017

12.8K
Robust Comparison of Protein Levels Across Tissues and Throughout Development Using Standardized Quantitative Western Blotting
08:13

Robust Comparison of Protein Levels Across Tissues and Throughout Development Using Standardized Quantitative Western Blotting

Published on: April 9, 2019

14.9K

Area of Science:

  • Biochemistry
  • Analytical Chemistry
  • Proteomics

Background:

  • Traditional proteomics workflows mandate protein quantification and physical normalization.
  • These steps add significant time, cost, and complexity, particularly for large-scale studies.
  • Computational normalization strategies are standard in proteomics data analysis.

Purpose of the Study:

  • To investigate the impact of omitting physical protein normalization on quantitative proteomics data.
  • To determine if computational normalization can compensate for the absence of physical normalization.
  • To identify potential time and cost savings in proteomics workflows.

Main Methods:

  • Comparison of quantitative proteomics data from samples with and without physical protein amount normalization.
  • Analysis of peptide and protein abundance variations.
  • Application of standard computational normalization techniques to both normalized and unnormalized datasets.

Main Results:

  • Increased variation in input protein amounts correlated with higher variance in output peptide and protein abundances.
  • Omitting physical normalization did not lead to unacceptable increases in measurement variability when computational normalization was applied.
  • The study established a relationship between input variation and output variance in quantitative proteomics.

Conclusions:

  • Protein quantification and physical normalization may be omitted in certain quantitative proteomics experiments.
  • Computational normalization effectively compensates for the lack of physical normalization in many cases.
  • This finding enables significant time and cost optimizations for proteomics workflows.