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...
Peptide Identification Using Tandem Mass Spectrometry01:33

Peptide Identification Using Tandem Mass Spectrometry

Tandem mass spectrometry, also known as MS/MS or MS2, is an analytical technique that employs two mass analyzers. Essentially it is a series of mass spectrometers that helps isolate a particular biomolecule and then helps study its chemical properties.
This technique helps gather information regarding the protein from which the peptide was obtained and to study the peptides’ amino acid sequence. Identifying peptides from a complex mixture is an important component of the growing field of...

You might also read

Related Articles

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

Sort by
Same author

Mutations within the predicted fragment-binding region of FAM83G/SACK1G abolish its interaction with the Ser/Thr kinase CK1α.

Open biology·2026
Same author

Disruption of the mRNA m6A writer complex triggers autoimmunity in Arabidopsis.

PLoS genetics·2025
Same author

LIGYSIS-web: a resource for the analysis of protein-ligand binding sites.

Nucleic acids research·2025
Same author

ICTV Virus Taxonomy Profile: <i>Adnaviria</i> 2025.

The Journal of general virology·2025
Same author

Protocol for sequence clustering with PaSiMap in Jalview.

STAR protocols·2025
Same author

Comparative evaluation of methods for the prediction of protein-ligand binding sites.

Journal of cheminformatics·2024
Same journal

Protein sequence-similarity search acceleration using a heuristic algorithm with a sensitive matrix.

Journal of structural and functional genomics·2017
Same journal

Toward the next step in G protein-coupled receptor research: a knowledge-driven analysis for the next potential targets in drug discovery.

Journal of structural and functional genomics·2017
Same journal

Special issue: big data analyses in structural and functional genomics.

Journal of structural and functional genomics·2017
Same journal

Classification of ligand molecules in PDB with graph match-based structural superposition.

Journal of structural and functional genomics·2016
Same journal

VaProS: a database-integration approach for protein/genome information retrieval.

Journal of structural and functional genomics·2016
Same journal

NLDB: a database for 3D protein-ligand interactions in enzymatic reactions.

Journal of structural and functional genomics·2016
See all related articles

Related Experiment Video

Updated: Jun 13, 2026

Navigating the Mass Spectrometry-Based Proteomic Data Using Free Computational Tools
07:01

Navigating the Mass Spectrometry-Based Proteomic Data Using Free Computational Tools

Published on: August 19, 2025

The Scottish Structural Proteomics Facility: targets, methods and outputs.

Muse Oke1, Lester G Carter, Kenneth A Johnson

  • 1Biomedical Sciences Research Complex, University of St Andrews, St Andrews, KY16 9ST, UK.

Journal of Structural and Functional Genomics
|April 27, 2010
PubMed
Summary
This summary is machine-generated.

The Scottish Structural Proteomics Facility successfully determined over 40 protein structures using high-throughput methods. This achievement highlights the balance between automation and expertise in structural biology research.

More Related Videos

Comprehensive Workflow of Mass Spectrometry-based Shotgun Proteomics of Tissue Samples
14:51

Comprehensive Workflow of Mass Spectrometry-based Shotgun Proteomics of Tissue Samples

Published on: November 13, 2021

Related Experiment Videos

Last Updated: Jun 13, 2026

Navigating the Mass Spectrometry-Based Proteomic Data Using Free Computational Tools
07:01

Navigating the Mass Spectrometry-Based Proteomic Data Using Free Computational Tools

Published on: August 19, 2025

Comprehensive Workflow of Mass Spectrometry-based Shotgun Proteomics of Tissue Samples
14:51

Comprehensive Workflow of Mass Spectrometry-based Shotgun Proteomics of Tissue Samples

Published on: November 13, 2021

Area of Science:

  • Structural Biology
  • Biochemistry
  • Proteomics

Background:

  • The Scottish Structural Proteomics Facility was established to advance high-throughput protein structure determination.
  • Previous methods for structure determination were not sufficiently high-throughput for the growing need for structural data.

Purpose of the Study:

  • To report on the development and outcomes of a laboratory-scale, high-throughput approach to protein structure determination.
  • To reflect on the efficiency, challenges, and impact of automated structural biology pipelines.

Main Methods:

  • Development of a laboratory-scale, high-throughput pipeline for protein structure determination.
  • Determination of over 40 protein structures.
  • Detailed reporting of experimental methods and deposition of structural data.

Main Results:

  • Successful determination of over 40 protein structures within a 5-year period.
  • Publication of ten peer-reviewed papers reporting structural data.
  • Generation of structural data exceeding the capacity for immediate in-depth analysis and publication.

Conclusions:

  • The facility demonstrated a successful high-throughput approach to protein structure determination.
  • Automation is valuable but requires significant scientific and technical expertise.
  • The project's impact is maximized by sharing experimental details and deposited structures for further biological investigation.