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

Covalently Linked Protein Regulators02:04

Covalently Linked Protein Regulators

9.6K
Proteins can undergo many types of post-translational modifications, often in response to changes in their environment. These modifications play an important role in the function and stability of these proteins. Covalently linked molecules include functional groups, such as methyl, acetyl, and phosphate groups, and also small proteins, such as ubiquitin. There are around 200 different types of covalent regulators that have been identified.
These groups modify specific amino acids in a protein....
9.6K
Covalently Linked Protein Regulators02:04

Covalently Linked Protein Regulators

2.0K
2.0K
X-linked Traits01:19

X-linked Traits

58.8K
In most mammalian species, females have two X sex chromosomes and males have an X and Y. As a result, mutations on the X chromosome in females may be masked by the presence of a normal allele on the second X. In contrast, a mutation on the X chromosome in males more often causes observable biological defects, as there is no normal X to compensate. Trait variations arising from mutations on the X chromosome are called “X-linked”.
58.8K
Enzyme-linked Receptors01:00

Enzyme-linked Receptors

86.7K
Enzyme-linked receptors are proteins that act as both receptor and enzyme, activating multiple intracellular signals. This is a large group of receptors that include the receptor tyrosine kinase (RTK) family. Many growth factors and hormones bind to and activate the RTKs.
Neurotrophin (NT) receptors are a family of RTKs, including trkA, trkB, and trkC (tropomyosin-related kinase) receptors. TrkA is specific for nerve growth factor (NGF), neurotrophin-6, and neurotrophin-7. TrkB binds...
86.7K
Sex-linked Disorders01:43

Sex-linked Disorders

109.0K
Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.
109.0K
Toxic Reactions: Overview01:26

Toxic Reactions: Overview

2.0K
When toxic substances penetrate the human body, they disseminate to various tissues, undergoing metabolic changes. This process yields reactive metabolites that may covalently bind with specific target molecules, resulting in toxicity.
Toxicity falls into two primary categories: local and systemic.
Local toxicity appears at the exposure site, such as protein denaturation caused by caustic substances.
In contrast, systemic toxicity requires the toxic agent's absorption and distribution,...
2.0K

You might also read

Related Articles

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

Sort by
Same author

Enhanced crystallinity of tetrahalopyridyl (THP) derivatized compounds.

Chemical science·2026
Same author

Salivary Antimicrobial Peptide Histatin-5 Does Not Display Zn(II)-Dependent or -Independent Activity against Streptococci.

ACS infectious diseases·2023
Same author

One-pot ester and thioester formation mediated by pentafluoropyridine (PFP).

Organic & biomolecular chemistry·2022
Same author

Aminoacyl chain translocation catalysed by a type II thioesterase domain in an unusual non-ribosomal peptide synthetase.

Nature communications·2022
Same author

Peptoids with Antibiofilm Activity against the Gram Negative Obligate Anaerobe, <i>Fusobacterium nucleatum</i>.

Molecules (Basel, Switzerland)·2021
Same author

Carboxylic Acid Deoxyfluorination and One-Pot Amide Bond Formation Using Pentafluoropyridine (PFP).

Organic letters·2021

Related Experiment Video

Updated: Feb 6, 2026

Synthesis and Mass Spectrometry Analysis of Oligo-peptoids
11:44

Synthesis and Mass Spectrometry Analysis of Oligo-peptoids

Published on: February 21, 2018

11.4K

Exploring the links between peptoid antibacterial activity and toxicity.

H L Bolt1, G A Eggimann1, C A B Jahoda2

  • 1Department of Chemistry , Durham University , South Road , Durham , DH1 3LE , UK .

Medchemcomm
|August 16, 2018
PubMed
Summary

This study profiles the toxicity of linear peptoids against mammalian cells, correlating cytotoxicity with antibacterial activity and hydrophobicity. Findings aid in designing safer, effective antimicrobial peptoids.

More Related Videos

An Efficient Method for the Synthesis of Peptoids with Mixed Lysine-type/Arginine-type Monomers and Evaluation of Their Anti-leishmanial Activity
12:02

An Efficient Method for the Synthesis of Peptoids with Mixed Lysine-type/Arginine-type Monomers and Evaluation of Their Anti-leishmanial Activity

Published on: November 2, 2016

12.6K
A Novel Method to Determine the Longitudinal Antibacterial Activity of Drug-Eluting Materials
06:18

A Novel Method to Determine the Longitudinal Antibacterial Activity of Drug-Eluting Materials

Published on: March 3, 2023

1.8K

Related Experiment Videos

Last Updated: Feb 6, 2026

Synthesis and Mass Spectrometry Analysis of Oligo-peptoids
11:44

Synthesis and Mass Spectrometry Analysis of Oligo-peptoids

Published on: February 21, 2018

11.4K
An Efficient Method for the Synthesis of Peptoids with Mixed Lysine-type/Arginine-type Monomers and Evaluation of Their Anti-leishmanial Activity
12:02

An Efficient Method for the Synthesis of Peptoids with Mixed Lysine-type/Arginine-type Monomers and Evaluation of Their Anti-leishmanial Activity

Published on: November 2, 2016

12.6K
A Novel Method to Determine the Longitudinal Antibacterial Activity of Drug-Eluting Materials
06:18

A Novel Method to Determine the Longitudinal Antibacterial Activity of Drug-Eluting Materials

Published on: March 3, 2023

1.8K

Area of Science:

  • Medicinal Chemistry
  • Biotechnology
  • Antimicrobial Research

Background:

  • Peptoids show potential as antimicrobial agents against diverse pathogens.
  • Limited toxicity data hinders rational design of effective antimicrobial peptoids.

Purpose of the Study:

  • To profile the toxicity of linear peptoids against mammalian cell lines.
  • To correlate peptoid cytotoxicity with antibacterial activity and hydrophobicity.

Main Methods:

  • Toxicity profiling using HaCaT and HepG2 mammalian cell lines.
  • Evaluation of antibacterial properties against Gram-positive and Gram-negative bacteria.
  • Correlation analysis of cytotoxicity, antibacterial activity, and peptoid hydrophobicity.

Main Results:

  • Established toxicity profiles for a series of linear peptoids.
  • Demonstrated correlation between peptoid hydrophobicity, cytotoxicity, and antimicrobial efficacy.
  • Identified key parameters for designing safer antimicrobial peptoids.

Conclusions:

  • Toxicity profiling is crucial for developing effective antimicrobial peptoids.
  • Hydrophobicity is a significant factor influencing both efficacy and safety.
  • This data supports the rational design of next-generation antimicrobial peptoids.