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HOST-[2] ROTAXANES: GUEST RECOGNITION AND CELLULAR TRANSPORT

HOUSE, BRIAN EDWARD

Abstract Details

2006, MS, University of Cincinnati, Arts and Sciences : Chemistry.
There continues to be a great demand for synthetic hosts that recognize targeted guests as efficiently as proteins recognize endogenous ligands. Artificial protein mimetics could act as chemical sensors, catalysts, or agents that transport drugs across cell membranes. We have created new protein mimetics with amino acid recognition elements that converge to a hydrophobic pocket in order to provide maximum binding free energy with a guest. The dynamic component of these host-[2]rotaxanes allows them to adjust to their environment, whether aqueous or non-aqueous, and does not detract significantly from the binding free energy. The host-[2]rotaxanes bind a variety of biomolecules like oligopeptides and some of them efficiently transport fluorescein and some fluoresceinated peptides into eukaryotic cells.
Dr. David Smithrud (Advisor)
28 p.

Recommended Citations

Citations

  • HOUSE, B. E. (2006). HOST-[2] ROTAXANES: GUEST RECOGNITION AND CELLULAR TRANSPORT [Master's thesis, University of Cincinnati]. OhioLINK Electronic Theses and Dissertations Center. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1155826127

    APA Style (7th edition)

  • HOUSE, BRIAN. HOST-[2] ROTAXANES: GUEST RECOGNITION AND CELLULAR TRANSPORT. 2006. University of Cincinnati, Master's thesis. OhioLINK Electronic Theses and Dissertations Center, http://rave.ohiolink.edu/etdc/view?acc_num=ucin1155826127.

    MLA Style (8th edition)

  • HOUSE, BRIAN. "HOST-[2] ROTAXANES: GUEST RECOGNITION AND CELLULAR TRANSPORT." Master's thesis, University of Cincinnati, 2006. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1155826127

    Chicago Manual of Style (17th edition)