Related Experiment Video

Updated: Apr 20, 2026

Multi-Faceted Mass Spectrometric Investigation of Neuropeptides in Callinectes sapidus
09:22

Multi-Faceted Mass Spectrometric Investigation of Neuropeptides in Callinectes sapidus

Published on: May 31, 2022

3.0K

Natural products: Getting a handle on peptides

Jaclyn M Winter1, Yi Tang2

  • 1Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, California 90095, USA.

Nature Chemistry
|November 21, 2014
PubMed
Summary

No abstract available in PubMed .

More Related Videos

Mass Spectrometry-Guided Genome Mining as a Tool to Uncover Novel Natural Products
11:13

Mass Spectrometry-Guided Genome Mining as a Tool to Uncover Novel Natural Products

Published on: March 12, 2020

11.7K
A Tripeptide-Stabilized Nanoemulsion of Oleic Acid
10:42

A Tripeptide-Stabilized Nanoemulsion of Oleic Acid

Published on: February 27, 2019

10.0K

Related Experiment Videos

Last Updated: Apr 20, 2026

Multi-Faceted Mass Spectrometric Investigation of Neuropeptides in Callinectes sapidus
09:22

Multi-Faceted Mass Spectrometric Investigation of Neuropeptides in Callinectes sapidus

Published on: May 31, 2022

3.0K
Mass Spectrometry-Guided Genome Mining as a Tool to Uncover Novel Natural Products
11:13

Mass Spectrometry-Guided Genome Mining as a Tool to Uncover Novel Natural Products

Published on: March 12, 2020

11.7K
A Tripeptide-Stabilized Nanoemulsion of Oleic Acid
10:42

A Tripeptide-Stabilized Nanoemulsion of Oleic Acid

Published on: February 27, 2019

10.0K

Related Concept Videos

Peptide Identification Using Tandem Mass Spectrometry01:33

Peptide Identification Using Tandem Mass Spectrometry

8.8K
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...
8.8K
Peptide Bonds02:43

Peptide Bonds

88.2K
A peptide bond covalently attaches amino acids through a dehydration reaction. One amino acid's carboxyl group and another amino acid's amino group combine, releasing a water molecule. The resulting bond is the peptide bond. The products that such linkages form are peptides. As more amino acids join this growing chain, the resulting chain is a polypeptide. Each polypeptide has a free amino group at one end. This end has the N-terminal, or the amino-terminal, and the other end has a free...
88.2K

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

ReGAIN: A bioinformatics platform for assessing probabilistic co-occurrence between resistance genes in bacterial pathogens.

Bioinformatics (Oxford, England)·2026

Genome Mining and Characterization of an Uncharacterized Monofunctional Class I Diterpene Synthase From a Marine-Derived Fungus.

Chembiochem : a European journal of chemical biology·2026

An extremophilic <i>Nocardiopsis</i> strain from Great Salt Lake expands the taxonomic range of mycolic acid biosynthesis.

bioRxiv : the preprint server for biology·2025

IDBac: an open-access web platform and compendium for the identification of bacteria by MALDI-TOF mass spectrometry.

bioRxiv : the preprint server for biology·2025

SeqForge: a scalable platform for alignment-based searches, motif detection, and sequence curation across meta/genomic datasets.

BMC bioinformatics·2025

SeqForge: A scalable platform for alignment-based searches, motif detection, and sequence curation across meta/genomic datasets.

bioRxiv : the preprint server for biology·2025

Programmable arene ring opening unlocks the diversification of phenols.

Nature chemistry·2026

A molecular model for the Ge(100) buckled dimer.

Nature chemistry·2026

Electrophilic amination-induced 1,2-boronate migration for the modular synthesis of β-amino boronic esters.

Nature chemistry·2026

Oxetane-to-azetidine skeletal editing.

Nature chemistry·2026

Genetically targeted photocatalytic organic dyes for spatiotemporally controlled organic synthesis in specific living cells.

Nature chemistry·2026

A rechargeable non-aqueous Mg-O<sub>2</sub> battery based on magnesium peroxide chemistry.

Nature chemistry·2026

Notoginsenoside R1 Alleviates Acetaminophen-Induced Liver Injury via MAPK/mTOR-Mediated Autophagy.

The American journal of Chinese medicine·2026

Tryptophan-Mediated Sodium Dodecyl Sulfate Binding to Proteins.

The protein journal·2026

Evolution of KRAS molecular glues: from allele-selective to Pan-RAS and protein-protein interaction modulators.

Acta pharmacologica Sinica·2026

Promiscuity of Cytochrome P450 Enzymes: Discovery Strategies, Mechanistic Insights, and Applications in Terpenoid Biosynthesis.

Journal of agricultural and food chemistry·2026

Topical Sirolimus Therapy for Agminated Pyogenic Granulomas: A Two-Case Report.

Pediatric dermatology·2026

HELM-BERT: Topology-Aware Representations for Chemically Modified Peptides.

Journal of chemical information and modeling·2026
See all related articles
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
Jove
Visualize
Contact Us