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

Maxam-Gilbert Sequencing01:05

Maxam-Gilbert Sequencing

In the same year as the discovery of the Sanger sequencing method, another group of scientists, Allan Maxam and Walter Gilbert, demonstrated their chemical-cleavage method for DNA sequencing. The Maxam-Gilbert method relies on using different chemicals that can cleave the DNA sequence at specific sites, the separation of resulting DNA fragments of variable size using electrophoresis, and deciphering the DNA sequence from the resulting gel bands.
Challenges of the Maxam-Gilbert Method
The...
Cycloaddition Reactions: MO Requirements for Thermal Activation01:16

Cycloaddition Reactions: MO Requirements for Thermal Activation

Thermal cycloadditions are reactions where the source of activation energy needed to initiate the reaction is provided in the form of heat. A typical example of a thermally-allowed cycloaddition is the Diels–Alder reaction, which is a [4 + 2] cycloaddition. In contrast, a [2 + 2] cycloaddition is thermally forbidden.
Cycloaddition Reactions: MO Requirements for Photochemical Activation01:12

Cycloaddition Reactions: MO Requirements for Photochemical Activation

Some cycloaddition reactions are activated by heat, while others are initiated by light. For example, a [2 + 2] cycloaddition between two ethylene molecules occurs only in the presence of light. It is photochemically allowed but thermally forbidden.
Protecting Groups for Aldehydes and Ketones: Introduction01:23

Protecting Groups for Aldehydes and Ketones: Introduction

Protecting groups are compounds that can bind to a specific functional group in the presence of other functional groups to protect them from undesired chemical reactions. These compounds can selectively bind to particular functional groups and advance chemoselective reactions in polyfunctional systems (Figure 1). After the functional group has served its purpose, it is removed by reacting it with specific compounds.
Molecular Models02:00

Molecular Models

Physical models representing molecular architectures of chemical compounds play essential roles in understanding chemistry. The use of molecular models makes it easier to visualize the structures and shapes of atoms and molecules.
¹H NMR: Pople Notation01:09

¹H NMR: Pople Notation

The Pople nomenclature system classifies spin systems based on the difference between their chemical shifts. Coupled spins are denoted by capital letters with subscripts indicating the number of equivalent nuclei. When the coupled nuclei have well-separated chemical shifts, they are assigned letters that are far apart in the alphabet, such as A and X. When the difference in chemical shifts is small, coupled nuclei are named using adjacent letters of the alphabet (AB, MN, or XY).
A proton...

You might also read

Related Articles

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

Sort by
Same author

On the Equivalence of Two-Point Basis-Set Extrapolations and Robust Parameterization for Coupled-Cluster and Double-Hybrid DFT Methods.

The journal of physical chemistry. A·2026
Same author

Electrolyte-Guided Selectivity Unlocks Pathway Control in Electrochemical Olefin Functionalization.

Journal of the American Chemical Society·2026
Same author

An exhaustive cell-based screen coupled with an intracellular-induced lux-based reporter identified bioactive molecules that inhibit host cell infection by intracellular pathogens.

Frontiers in cellular and infection microbiology·2026
Same author

Radiative cooling of isolated Al-5 cluster ions observed on ultralong timescales as a test case for the validity of the harmonic cascade model.

Physical chemistry chemical physics : PCCP·2026
Same author

A pharmacological modality to sequester homomeric proteins.

Nature chemical biology·2026
Same author

Bridging or exchanging partners? A supramolecular perspective on bifunctional molecules and their potential for triggerable enzyme therapy.

Current opinion in chemical biology·2026

Related Experiment Video

Updated: May 7, 2026

Creating Highly Specific Chemically Induced Protein Dimerization Systems by Stepwise Phage Selection of a Combinatorial Single-Domain Antibody Library
10:17

Creating Highly Specific Chemically Induced Protein Dimerization Systems by Stepwise Phage Selection of a Combinatorial Single-Domain Antibody Library

Published on: January 14, 2020

Authorizing multiple chemical passwords by a combinatorial molecular keypad lock.

Bhimsen Rout1, Petr Milko, Mark A Iron

  • 1Departments of †Organic Chemistry and ‡Chemical Research Support, Weizmann Institute of Science , Rehovot 76100, Israel.

Journal of the American Chemical Society
|October 4, 2013
PubMed
Summary

A novel fluorescent molecular sensor acts as a sophisticated security system. This sensor can process various chemical inputs, enabling the creation of highly secure, unbreakable molecular combination locks.

More Related Videos

Plasmid-derived DNA Strand Displacement Gates for Implementing Chemical Reaction Networks
07:50

Plasmid-derived DNA Strand Displacement Gates for Implementing Chemical Reaction Networks

Published on: November 25, 2015

Related Experiment Videos

Last Updated: May 7, 2026

Creating Highly Specific Chemically Induced Protein Dimerization Systems by Stepwise Phage Selection of a Combinatorial Single-Domain Antibody Library
10:17

Creating Highly Specific Chemically Induced Protein Dimerization Systems by Stepwise Phage Selection of a Combinatorial Single-Domain Antibody Library

Published on: January 14, 2020

Plasmid-derived DNA Strand Displacement Gates for Implementing Chemical Reaction Networks
07:50

Plasmid-derived DNA Strand Displacement Gates for Implementing Chemical Reaction Networks

Published on: November 25, 2015

Area of Science:

  • Chemistry
  • Molecular Engineering
  • Biotechnology

Background:

  • Molecular sensors are crucial for detecting and analyzing chemical substances.
  • Developing secure systems at the molecular level presents significant challenges.
  • Existing security systems lack the adaptability and complexity of biological systems.

Purpose of the Study:

  • To demonstrate a combinatorial fluorescent molecular sensor as a high-efficiency molecular security system.
  • To showcase the capability of pattern-generating molecules in processing diverse chemical inputs.
  • To explore the potential for creating unbreakable combination locks at the molecular scale.

Main Methods:

  • Utilizing a pattern-generating molecule to process chemical inputs.
  • Discriminating among different concentrations of chemical inputs.
  • Forming multivalent and kinetically stable complexes for signal generation.

Main Results:

  • The molecular sensor successfully processed diverse sets of chemical inputs.
  • The system demonstrated discrimination capabilities based on chemical concentrations.
  • Multivalent and kinetically stable complexes were formed, indicating successful pattern recognition.

Conclusions:

  • Combinatorial fluorescent molecular sensors offer a powerful tool for molecular security.
  • The demonstrated system can process a wide range of chemical "passwords" of varying lengths.
  • This approach holds significant potential for developing unbreakable molecular combination locks.