Delivery of mirror image polypeptides into cells

Mirror image peptides have unique stability and immunogenic properties in mammals, making them attractive agents to investigate. Their properties inside cells have been mostly unexplored because biopolymers are difficult to transport across cellular membranes. Here, we used protective antigen (PA) f...

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Bibliographic Details
Main Authors: Rabideau, Amy E. (Contributor), Liao, Xiaoli (Contributor), Pentelute, Bradley L. (Contributor)
Other Authors: Massachusetts Institute of Technology. Department of Chemistry (Contributor)
Format: Article
Language:English
Published: Royal Society of Chemistry, The, 2015-02-25T19:47:43Z.
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Online Access:Get fulltext
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042 |a dc 
100 1 0 |a Rabideau, Amy E.  |e author 
100 1 0 |a Massachusetts Institute of Technology. Department of Chemistry  |e contributor 
100 1 0 |a Rabideau, Amy E.  |e contributor 
100 1 0 |a Pentelute, Bradley L.  |e contributor 
100 1 0 |a Liao, Xiaoli  |e contributor 
700 1 0 |a Liao, Xiaoli  |e author 
700 1 0 |a Pentelute, Bradley L.  |e author 
245 0 0 |a Delivery of mirror image polypeptides into cells 
260 |b Royal Society of Chemistry, The,   |c 2015-02-25T19:47:43Z. 
856 |z Get fulltext  |u http://hdl.handle.net/1721.1/95627 
520 |a Mirror image peptides have unique stability and immunogenic properties in mammals, making them attractive agents to investigate. Their properties inside cells have been mostly unexplored because biopolymers are difficult to transport across cellular membranes. Here, we used protective antigen (PA) from anthrax toxin to deliver mirror image polypeptide cargo into the cytosol of mammalian cells when conjugated to the C-terminus of the PA-binding domain of lethal factor, LF[subscript N]. We found mirror image polypeptides and proteins were translocated as efficiently into cells as their L counterparts. Once in the cytosol, by the use of western blot, we found that D peptides at the C-terminus of LF[subscript N] were able to achieve higher steady state concentrations when compared to the L-peptide conjugate. With this platform, we delivered a D-peptide MDM2 antagonist to disrupt the p53/MDM2 interaction in cancer cells. For the first time, we show the PA/LF[subscript N] system is adaptable for the intracellular delivery of mirror image peptides and proteins. 
520 |a Massachusetts Institute of Technology (Charles E. Reed Faculty Initiative Fund) 
520 |a Damon Runyon Cancer Research Foundation (Innovation Award) 
520 |a National Science Foundation (U.S.) (Career Award CHE-1351807) 
520 |a National Science Foundation (U.S.). Graduate Research Fellowship Program 
520 |a New England Regional Center of Excellence for Biodefense and Emerging Infectious Diseases 
520 |a Massachusetts Institute of Technology. Biophysical Instrumentation Facility 
546 |a en_US 
655 7 |a Article 
773 |t Chemical Science