Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Karen L. Buchmueller"'
Publikováno v:
The FASEB Journal. 32
Autor:
W. David Wilson, Caroline O'Hare, Daniel Hochhauser, Zarmeen T. Taherbhai, Moses Lee, Suzanna L. Bailey, Cameron M. Howard, Binh Nguyen, Karen L. Buchmueller, John A. Hartley
Publikováno v:
ChemBioChem. 6:2305-2311
A novel hairpin polyamide, ZT65B, containing a 3-methylpicolinate moiety was designed to target the inverted CCAAT box (ICB) of the human multidrug resistance 1 gene (MDR1) promoter. Binding of nuclear factor-Y (NF-Y) to the ICB site upregulates MDR1
Autor:
Cameron M. Howard, James A. Henry, N. M. Le, Moses Lee, Peter B. Uthe, Suzanna L. Bailey, Karen L. Buchmueller, Andrew M. Staples, Sarah M. Horick, Kari K. Cox
Publikováno v:
Letters in Drug Design & Discovery. 2:137-142
Autor:
N. Minh Le, Peter B. Uthe, Andrew M. Staples, Binh Nguyen, Cameron M. Howard, Karen L. Buchmueller, W. David Wilson, Kari K. Cox, Sarah M. Horick, Moses Lee, Kimberly A. O. Pacheco
Publikováno v:
Journal of the American Chemical Society. 127:742-750
Pyrrole (Py) and imidazole (Im) polyamides can be designed to target specific DNA sequences. The effect that the pyrrole and imidazole arrangement, plus DNA sequence, have on sequence specificity and binding affinity has been investigated using DNA m
Autor:
Cameron M. Howard, Binh Nguyen, Sarah M. Horick, Suzanna L. Bailey, Daniel Hochhauser, N. M. Le, James A. Henry, Moses Lee, Karen L. Buchmueller, Minal Kotecha, John A. Hartley, W. D. Wilson
Publikováno v:
Biochemistry. 43:12249-12257
The topoisomerase IIalpha promoter is regulated through transcription factor interactions with five inverted CCAAT boxes (ICBs). In confluent cancer cells, binding of nuclear factor Y to ICB2 represses the expression of this gene, contributing to res
Publikováno v:
Journal of the American Chemical Society. 125:10850-10861
Arylazide mediated photocrosslinking has been widely used to obtain structural constraints in biological systems, even though the reactive species generated upon photolysis in aqueous solution have not been well characterized. We establish a mechanis
Autor:
Karen L. Buchmueller, Austin E. Smith
Publikováno v:
Biochemistry. 50(38)
The molecular mechanism for the displacement of HMGA1 proteins from DNA is integral to disrupting their cellular function, which is linked to many metastatic cancers. Chemical shift and NOESY NMR experiments provide structural evidence for the displa
Autor:
Karen L. Buchmueller, Caroline O'Hare, David A. Matthews, Zachary S. Davis, Suzanna L. Bailey, Zarmeen T. Taherbhai, Moses Lee, John A. Hartley, Chrystal D. Bruce, Janna K. Register
Publikováno v:
Biochemistry. 45(45)
The polyamide f-ImPyIm has a higher affinity for its cognate DNA than either the parent analogue, distamycin A (10-fold), or the structural isomer, f-PyImIm (250-fold), has for its respective cognate DNA sequence. These findings have led to the formu
Autor:
Jerome Kluza, John A. Hartley, Caroline O'Hare, Karen L. Buchmueller, Jim S. Sexton, Peter B. Uthe, Daniel Hochhauser, Lloyd V. Flores, Andrew M. Staples, W. David Wilson, Cameron M. Howard, Hilary Mackay, Moses Lee
Publikováno v:
Chembiochem : a European journal of chemical biology. 7(11)
The synthesis and DNA-binding properties of a novel naphthalimide-polyamide hairpin (3) designed to target the inverted CCAAT box 2 (ICB2) site on the topoisomerase IIalpha (topoIIalpha) promoter are described. The polyamide component of 3 was derive
Autor:
Zarmeen T. Taherbhai, Justin B. Jones, Michelle Stewart, Caroline O'Hare, David Wilson, Toni Brown, Binh Nguyen, Hilary Mackay, Moses Lee, Jerome Kluza, Lindsay Stallings, John A. Hartley, Mark Turlington, Karen L. Buchmueller, Jim S. Sexton, Arden Sutterfield
Publikováno v:
Bioorganicmedicinal chemistry. 15(1)
Five polyamide derivatives with rationally modified C-terminus moieties were synthesized and their DNA binding specificity and affinity determined. A convergent approach was employed to synthesize polyamides containing an alkylaminopiperazine (4 and