4.7 Review

HaloTag Technology: A Versatile Platform for Biomedical Applications

Journal

BIOCONJUGATE CHEMISTRY
Volume 26, Issue 6, Pages 975-986

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.bioconjchem.5b00191

Keywords

-

Funding

  1. University of Wisconsin Madison
  2. Department of Defense [W81XWH-11-1-0644]
  3. National Institutes of Health [NIBIB/NCI R01CA169365, P30CA014520, T32CA009206]
  4. American Cancer Society [125246-RSG-13-099-01-CCE]

Ask authors/readers for more resources

Exploration of protein function and interaction is critical for discovering links among genomics, proteomics, and disease state; yet, the immense complexity of proteomics found in biological systems currently limits our investigational capacity. Although affinity and autofluorescent tags are widely employed for protein analysis, these methods have been met with limited success because they lack specificity and require multiple fusion tags and genetic constructs. As an alternative approach, the innovative HaloTag protein fusion platform allows protein function and interaction to be comprehensively analyzed using a single genetic construct with multiple capabilities. This is accomplished using a simplified process, in which a variable HaloTag ligand binds rapidly to the HaloTag protein (usually linked to the protein of interest) with high affinity and specificity. In this review, we examine all current applications of the HaloTag technology platform for biomedical applications, such as the study of protein isolation and purification, protein function, protein protein and protein DNA interactions, biological assays, in vitro cellular imaging, and in vivid molecular imaging. In addition, novel uses of the HaloTag platform are briefly discussed along with potential future applications.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available