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 Microarrays02:34

DNA Microarrays

Microarrays are high-throughput and relatively inexpensive assays that can be automated to analyze large quantities of data at a time. They are used in genome-wide studies to compare gene or protein expression under two varied conditions, such as healthy and diseased states. Microarrays consist of glass or silica slides on which probe molecules are covalently attached through surface functionalization. Most commonly, the slides are prepared through the chemisorption of silanes to silica...
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...
Protein Networks02:26

Protein Networks

An organism can have thousands of different proteins, and these proteins must cooperate to ensure the health of an organism. Proteins bind to other proteins and form complexes to carry out their functions. Many proteins interact with multiple other proteins creating a complex network of protein interactions.
These interactions can be represented through maps depicting protein-protein interaction networks, represented as nodes and edges. Nodes are circles that are representative of a protein,...

You might also read

Related Articles

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

Sort by
Same author

Anti-Epstein-Barr virus (EBV) antibodies in EBV-associated gastric carcinoma.

Infectious agents and cancer·2026
Same author

Highly Sensitive Spatial Proteomics with Multicolor Cleavable Fluorescent Tyramide.

Chemical & biomedical imaging·2025
Same author

Large-Scale Saliva-Based Clinical Surveillance Enables Real Time SARS-CoV-2 Outbreak Detection and Genomic Tracking (Arizona, 2020-2023).

Diagnostics (Basel, Switzerland)·2025
Same author

Nucleic Acid Programmable Protein Arrays for Autoantibody Discovery: A Step-by-Step Guide.

Methods in molecular biology (Clifton, N.J.)·2025
Same author

Progressive multifocal leukoencephalopathy and BK virus-nephropathy with bispecific antibody therapy in multiple myeloma.

Haematologica·2025
Same author

RAD18 methylation by the methyltransferase SETD6 attenuates DNA breaks.

Scientific reports·2025
Same journal

De Novo Protein Design Using the Blueprint Builder in Rosetta.

Current protocols in protein science·2020
Same journal

Methods for Expression of Recombinant Proteins Using a Pichia pastoris Cell-Free System.

Current protocols in protein science·2020
Same journal

Histone Purification Combined with High-Resolution Mass Spectrometry to Examine Histone Post-Translational Modifications and Histone Variants in Caenorhabditis elegans.

Current protocols in protein science·2020
Same journal

A Rapid and Facile Purification Method for Glycan-Binding Proteins and Glycoproteins.

Current protocols in protein science·2020
Same journal

Synthesis of Recombinant Human Hemoglobin With NH<sub>2</sub> -Terminal Acetylation in Escherichia coli.

Current protocols in protein science·2020
Same journal

A Fluorescence-Based Assay to Monitor SUMOylation in Real-Time.

Current protocols in protein science·2020
See all related articles

Related Experiment Video

Updated: Jun 2, 2026

Probing High-density Functional Protein Microarrays to Detect Protein-protein Interactions
08:07

Probing High-density Functional Protein Microarrays to Detect Protein-protein Interactions

Published on: August 2, 2015

Nucleic Acid programmable protein arrays: versatile tools for array-based functional protein studies.

Shane Miersch1, Joshua LaBaer

  • 1Biodesign Institute at Arizona State University, Tempe, Arizona.

Current Protocols in Protein Science
|April 14, 2011
PubMed
Summary
This summary is machine-generated.

The Nucleic Acid Programmable Protein Array (NAPPA) platform overcomes limitations of traditional protein microarrays. NAPPA enables in situ protein expression for diverse functional studies, offering a accessible and versatile research tool.

More Related Videos

Kinase Inhibitor Screening In Self-assembled Human Protein Microarrays
13:22

Kinase Inhibitor Screening In Self-assembled Human Protein Microarrays

Published on: October 23, 2019

Identifying Protein-protein Interaction Sites Using Peptide Arrays
07:44

Identifying Protein-protein Interaction Sites Using Peptide Arrays

Published on: November 18, 2014

Related Experiment Videos

Last Updated: Jun 2, 2026

Probing High-density Functional Protein Microarrays to Detect Protein-protein Interactions
08:07

Probing High-density Functional Protein Microarrays to Detect Protein-protein Interactions

Published on: August 2, 2015

Kinase Inhibitor Screening In Self-assembled Human Protein Microarrays
13:22

Kinase Inhibitor Screening In Self-assembled Human Protein Microarrays

Published on: October 23, 2019

Identifying Protein-protein Interaction Sites Using Peptide Arrays
07:44

Identifying Protein-protein Interaction Sites Using Peptide Arrays

Published on: November 18, 2014

Area of Science:

  • Biochemistry
  • Molecular Biology
  • Genomics

Background:

  • Protein microarrays are valuable for studying gene product function.
  • Technical challenges with purified protein stability and dynamic range limit their use.
  • Existing methods hinder broad adoption of protein microarrays.

Purpose of the Study:

  • Introduce the Nucleic Acid Programmable Protein Array (NAPPA) as an alternative to traditional protein microarrays.
  • Detail the construction and application of the NAPPA platform.
  • Provide a reference for generating and utilizing NAPPA-based microarrays.

Main Methods:

  • Spotting protein-encoding plasmid DNA onto an array surface.
  • Utilizing cell-free expression systems for in situ protein generation.
  • Employing array printing and laser slide scanning for construction.

Main Results:

  • NAPPA circumvents limitations of spotted protein arrays.
  • The platform enables diverse functional protein studies (e.g., protein-small molecule interactions).
  • NAPPA is adaptable to various capture modalities and expression systems.

Conclusions:

  • NAPPA offers a viable alternative for functional protein studies.
  • The platform is accessible to labs with standard equipment.
  • NAPPA facilitates applications like screening for antibody biomarkers.