The goal of this proposal is to further the development a novel strategy for the manipulation and labeling of the interior of living eukaryotic cells for research, diagnostic and therapeutic purposes. Cell-penetrating peptides (CPPs, also called protein transduction domains, or PTDs) offer the tantalizing prospect of exogenously delivering user-defined protein (and other biomolecular) cargos through the plasma membranes of eukaryotic cells. We have designed a CPP-adaptor fusion protein, TAT-Calmodulin (TAT-CaM), that consists of the cell penetrating moiety from HIV transactivator of transcription and human calmodulin. TAT- CaM binds CaM binding-site (CBS) containing cargos with nanomolar affinity in the presence of calcium but negligibly in its absence. Because mammalian cells typically maintain low resting concentrations of calcium, cargos dissociate from the CPP-adaptor once inside the cell. Current CPP strategies rely on covalent crosslinking or nonspecific hydrophobic interactions, fail to escape endosomes and only deliver a very small percentage of cargo molecules. Our CPP-adaptors represent a significant advance in cell-penetration technology because of the dissociation of cargo, allowing more ready manipulation of the internal environments of cells. We will use our CPP-adaptor and similar constructs to investigate the basic mechanistic details of CPP penetration of and trafficking through cells such as mode of penetrance, kinetics, and toxicity We will also utilize them to deliver cargo molecules that will demonstrate the utility of our system and its advantages over transfection, namely efficiency, speed and tunability and address biomedical research questions at KSU and other institutions. Success in these endeavors will validate that our strategy is an adaptable tool for delivery of a wide array of macromolecules, potentially improving the delivery of cancer therapeutics, antivirals, and proteins to ameliorate a variety of disorders as well as creating versatile research and diagnostic tools

Public Health Relevance

Cell-penetrating peptides offer the tantalizing prospect of exogenously delivering user-defined macromolecular cargos through the membranes of eukaryotic cells. Our innovative core technology is based on cell-penetrating peptide-coupled adaptor proteins that allow the spontaneous loading of almost any desired cargo protein for rapid delivery into cells. We will gain understanding of the mode of entry and subcellular trafficking of CPPs and cargos and develop innovative assays for an array of research questions.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
1R15GM120691-01
Application #
9171796
Study Section
Biochemistry and Biophysics of Membranes Study Section (BBM)
Program Officer
Ainsztein, Alexandra M
Project Start
2016-08-15
Project End
2019-07-31
Budget Start
2016-08-15
Budget End
2019-07-31
Support Year
1
Fiscal Year
2016
Total Cost
$401,792
Indirect Cost
$101,792
Name
Kennesaw State University
Department
Other Basic Sciences
Type
Schools of Arts and Sciences
DUNS #
627758923
City
Kennesaw
State
GA
Country
United States
Zip Code
30144
Ngwa, Verra M; Axford, David S; Healey, Allison N et al. (2017) A versatile cell-penetrating peptide-adaptor system for efficient delivery of molecular cargos to subcellular destinations. PLoS One 12:e0178648
LeCher, Julia C; Nowak, Scott J; McMurry, Jonathan L (2017) Breaking in and busting out: cell-penetrating peptides and the endosomal escape problem. Biomol Concepts 8:131-141