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

DNA Base Pairing02:27

DNA Base Pairing

33.1K
Erwin Chargaff’s rules on DNA equivalence paved the way for the discovery of base pairing in DNA. Chargaff’s rules state that in a double-stranded DNA molecule,
33.1K
DNA Base Pairing02:27

DNA Base Pairing

32.1K
32.1K
Base-pairing and DNA Repair02:27

Base-pairing and DNA Repair

91.0K
91.0K
From DNA to Protein03:06

From DNA to Protein

22.3K
The flow of genetic information in cells from DNA to mRNA to protein is described by the central dogma, which states that genes specify the sequence of mRNAs, which in turn specify the sequence of amino acids making up all proteins. The decoding of one molecule to another is performed by specific proteins and RNAs. Because the information stored in DNA is so central to cellular function, it makes intuitive sense that the cell would make mRNA copies of this information for protein synthesis...
22.3K
DNA Helicases00:55

DNA Helicases

24.0K
DNA unwinding helicase enzymes are a type of motor protein. Motor proteins can translocate along filaments or polymers using energy generated from ATP hydrolysis. Helicases are involved in all the important cellular processes where DNA unwinding is required, such as DNA replication, repair, recombination, and transcription. They are present in all living organisms, but vary in their structure, function, and mechanism of action. For example, in prokaryotes, DnaB helicase binds and translocates...
24.0K
DNA-only Transposons02:57

DNA-only Transposons

17.4K
DNA-only transposons are called autonomous transposons since they code for the enzyme transposase that is required for the transposition mechanism. Insertion of transposons can alter gene functions in multiple ways. They can mutate the gene, alter gene expression by introducing a novel promoter or insulator sequence, introduce new splice sites, and change the mRNA transcripts produced, or remodel chromatin structure.
The donor site from where the transposon is excised is either degraded or...
17.4K

You might also read

Related Articles

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

Sort by
Same author

5-ALA in Oncology: Current Clinical Applications, Biological Limitations, and Emerging Translational Strategies.

Biomedicines·2026
Same author

Aptagel Plasmonic Fiber Optic Biosensor for <i>In Vivo</i> Continuous Drug Monitoring.

ACS sensors·2026
Same author

Efficient algorithm for optimal wavelength selection in photoacoustic spectral unmixing.

Biomedical optics express·2026
Same author

Atherosclerotic Plaque Characterization Magnetic Resonance Imaging In Vitro at 1.5 Tesla for the Assessment of Coronary Artery Disease.

Journal of clinical medicine·2026
Same author

Contrasting temporal dynamics of fluorescence and photoacoustic signals from Cetuximab-IRDye800 conjugate in EGFR-overexpressing tumors.

Science advances·2026
Same author

Deep Learning and Cardiovascular Diseases: An Updated Narrative Review.

Journal of clinical medicine·2026

Related Experiment Video

Updated: Jan 26, 2026

Imaging of In Situ Interferon Gamma Production in the Mouse Spleen following Listeria monocytogenes Infection
09:11

Imaging of In Situ Interferon Gamma Production in the Mouse Spleen following Listeria monocytogenes Infection

Published on: July 16, 2019

9.6K

DNA-Based Photoacoustic Nanosensor for Interferon Gamma Detection.

Jennifer Morales1, Robert H Pawle2, Namik Akkilic3

  • 1Department of Bioengineering , Northeastern University , Boston , Massachusetts 02115 , United States.

ACS Sensors
|April 12, 2019
PubMed
Summary

Researchers developed a novel DNA nanosensor for detecting interferon gamma using photoacoustics. This tool offers real-time protein monitoring for improved medical diagnostics and disease research.

Keywords:
DNAcytokineinterferon-gammananophotoacousticphthalocyaninesensor

More Related Videos

Nanosensors to Detect Protease Activity In Vivo for Noninvasive Diagnostics
10:50

Nanosensors to Detect Protease Activity In Vivo for Noninvasive Diagnostics

Published on: July 16, 2018

16.9K
Optimized Interferon-gamma ELISpot Assay to Measure T Cell Responses in the Guinea Pig Model after Vaccination
08:13

Optimized Interferon-gamma ELISpot Assay to Measure T Cell Responses in the Guinea Pig Model after Vaccination

Published on: January 20, 2019

22.5K

Related Experiment Videos

Last Updated: Jan 26, 2026

Imaging of In Situ Interferon Gamma Production in the Mouse Spleen following Listeria monocytogenes Infection
09:11

Imaging of In Situ Interferon Gamma Production in the Mouse Spleen following Listeria monocytogenes Infection

Published on: July 16, 2019

9.6K
Nanosensors to Detect Protease Activity In Vivo for Noninvasive Diagnostics
10:50

Nanosensors to Detect Protease Activity In Vivo for Noninvasive Diagnostics

Published on: July 16, 2018

16.9K
Optimized Interferon-gamma ELISpot Assay to Measure T Cell Responses in the Guinea Pig Model after Vaccination
08:13

Optimized Interferon-gamma ELISpot Assay to Measure T Cell Responses in the Guinea Pig Model after Vaccination

Published on: January 20, 2019

22.5K

Area of Science:

  • Biomedical Engineering
  • Molecular Biology
  • Nanotechnology

Background:

  • Protein level monitoring is crucial for understanding physiological roles, homeostasis, and diseases.
  • Interferon gamma is a clinically relevant protein with key immunoregulatory functions.
  • Continuous in vivo protein monitoring tools are needed for real-time patient assessment.

Purpose of the Study:

  • To develop a DNA-based nanosensor for the photoacoustic detection of interferon gamma.
  • To create a proof-of-concept sensor for in vivo protein tracking.
  • To adapt the technology for detecting other proteins of interest.

Main Methods:

  • Development of a DNA nanosensor incorporating receptors and a phthalocyanine dye.
  • Utilizing photoacoustic detection for signal generation.
  • Surface plasmon resonance kinetic analysis to assess sensor performance.

Main Results:

  • The nanosensor demonstrated responsiveness and reversibility to interferon gamma with nanomolar affinity (KD1 = 167 nM, KD2 = 316 nM).
  • A novel phthalocyanine dye, when J-aggregated, increased the photoacoustic signal by 22.5%.
  • DNA structure bending upon receptor binding induced dye stacking, increasing the photoacoustic signal by 55% in the presence of 10 μM interferon gamma.

Conclusions:

  • A novel DNA-based photoacoustic nanosensor for interferon gamma detection was successfully developed.
  • The sensor exhibits high sensitivity and specificity, with potential for adaptation to other protein targets.
  • This technology represents a significant advancement for in vivo protein monitoring in research and medicine.