J. Wise

发表

Intein-mediated fusion expression, high efficient refolding, and one-step purification of gelonin toxin.

Chenyun Guo, Yawei Shi, Zhuoyu Li, 2004, Protein expression and purification.

Investigating the structure of nucleotide binding sites on the chloroplast F1-ATPase using electron spin resonance spectroscopy

P. Vogel, R. Lösel, A. Erbse, 1996 .

Trypsin cleavage of the alpha-subunit of beef heart F1-ATPase abolishes ATP synthesis and ATP-driven energy-transduction capabilities.

A. E. Senior, L. Latchney, J. Wise, 1981, Biochimica et biophysica acta.

Phosphatidylcholine activation of human heart (R)-3-hydroxybutyrate dehydrogenase mutants lacking active center sulfhydryls: site-directed mutagenesis of a new recombinant fusion protein.

W. Trommer, D. Chelius, A. Marks, 2000, Biochemistry.

Subunit b-dimer of the Escherichia coli ATP synthase can form left-handed coiled-coils.

P. Vogel, J. Wise, 2008, Biophysical journal.

Targeted inhibitors of P-glycoprotein increase chemotherapeutic-induced mortality of multidrug resistant tumor cells

N. Williams, P. Vogel, Courtney A. Follit, 2018, Scientific Reports.

Novel immunotoxin: a fusion protein consisting of gelonin and an acetylcholine receptor fragment as a potential immunotherapeutic agent for the treatment of Myasthenia gravis.

W. Trommer, P. Vogel, Yawei Shi, 2006, Protein expression and purification.

Specificity of the proton adenosinetriphosphatase of Escherichia coli for adenine, guanine, and inosine nucleotides in catalysis and binding.

A. E. Senior, L. Latchney, D. Perlin, 1984, Biochemistry.

Prolonged inhibition of P-glycoprotein after exposure to chemotherapeutics increases cell mortality in multidrug resistant cultured cancer cells

P. Vogel, Amila K Nanayakkara, J. Wise, 2019, PloS one.

Optimizing targeted inhibitors of P-glycoprotein using computational and structure guided approaches.

A. Lippert, P. Vogel, Alexander R. Lippert, 2019, Journal of medicinal chemistry.

Targeted inhibitors of P-glycoprotein increase chemotherapeutic-induced mortality of multidrug resistant tumor cells

N. Williams, P. Vogel, Courtney A. Follit, 2018, Scientific Reports.

The proton-ATPase of bacteria and mitochondria

A. E. Senior, J. Wise, 2005, The Journal of Membrane Biology.

In silico identified targeted inhibitors of P-glycoprotein overcome multidrug resistance in human cancer cells in culture

P. Vogel, J. G. Wise, Courtney A. Follit, 2015, Pharmacology research & perspectives.

In Silico Screening for Inhibitors of P-Glycoprotein That Target the Nucleotide Binding Domains

P. Vogel, Courtney A. Follit, F. Brewer, 2014, Molecular Pharmacology.

Cationic branched polymers for cellular delivery of negatively charged cargo.

P. Vogel, Shannon R. Woodruff, N. Tsarevsky, 2017, Journal of drug delivery science and technology.

Tight divalent cation-binding sites of soluble adenosine triphosphatase (F1) from beef heart mitochondria and Escherichia coli.

A. E. Senior, J. Wise, L. Richardson, 1980, The Journal of biological chemistry.

Combinatorial Redesign of the DNA Binding Specificity of a Prokaryotic Helix-Turn-Helix Repressor

P. Vogel, Pia D. Vogel, John G. Wise, 2003, Journal of bacteriology.

Transport Dynamics of MtrD: an RND Multidrug Efflux Pump from Neisseria gonorrhoeae

J. Wise, Chanyang Park, Lauren Ammerman, 2021, bioRxiv.

Catalytic properties of the F1-adenosine triphosphatase from Escherichia coli K-12 and its genetic variants as revealed by 18O exchanges.

P. Boyer, A. E. Senior, J. M. Wood, 1987, The Journal of biological chemistry.

Accommodating discontinuities in dimeric left-handed coiled coils in ATP synthase external stalks.

P. Vogel, J. G. Wise, J. Wise, 2009, Biophysical journal.

Structure of the cytosolic part of the subunit b-dimer of Escherichia coli F0F1-ATP synthase.

S. Delannoy, P. Vogel, T. Hornung, 2008, Biophysical journal.

The Subunit b Dimer of the FoF1-ATP Synthase

S. Dunn, P. Vogel, T. Hornung, 2004, Journal of Biological Chemistry.

Conformational changes in the Escherichia coli ATP synthase b-dimer upon binding to F1-ATPase

P. Vogel, T. Hornung, O. Volkov, 2008, Journal of bioenergetics and biomembranes.

Defective proton ATPase of uncA mutants of Escherichia coli. 5'-Adenylyl imidodiphosphate binding and ATP hydrolysis.

A. M. Ferguson, A. E. Senior, L. Latchney, 1984, Biochemistry.

Purification of F1-ATPase with impaired catalytic activity from partial revertants of Escherichia coli uncA mutant strains.

A. M. Ferguson, A. E. Senior, L. Latchney, 1984, Archives of biochemistry and biophysics.

The defective proton-ATPase of uncA mutants of Escherichia coli. Studies of nucleotide binding sites, bound aurovertin fluorescence, and labeling of essential residues of the purified F1-ATPase.

A. E. Senior, L. Latchney, J. G. Wise, 1981, The Journal of biological chemistry.

Multiple Drug Transport Pathways through Human P-Glycoprotein.

P. Vogel, J. McCormick, J. Wise, 2015, Biochemistry.

Catalytic Transitions in the Human MDR1 P-Glycoprotein Drug Binding Sites

John G. Wise, J. Wise, 2012, Biochemistry.

Transport of Alzheimer’s associated amyloid-β catalyzed by P-glycoprotein

P. Vogel, Gang Chen, J. McCormick, 2020, bioRxiv.

Catalytic properties of the Escherichia coli proton adenosinetriphosphatase: evidence that nucleotide bound at noncatalytic sites is not involved in regulation of oxidative phosphorylation.

A. E. Senior, J. Wise, 1985, Biochemistry.

Catalytic and Noncatalytic Nucleotide Binding Sites of F1-ATPases: Probes of Location, Structure and Function by Use of 2-N3-ATP

P. Boyer, R. L. Cross, Z. Xue, 1989 .

Conversion of .lambda. phage Cro into an operator-specific nuclease

T. W. Bruice, D. Sigman, D. Rosser, 1991 .

New aspects on the mechanism of GroEL-assisted protein folding.

S. Neuhofen, P. Vogel, C. Coan, 2002, Biochimica et Biophysica Acta.

Effects of magnesium ions on the relative conformation of nucleotide binding sites of F1-ATPases as studied by electron spin resonance spectroscopy.

Y. Kagawa, W. Trommer, H. Schäfer, 1994, The Journal of biological chemistry.

Catalytic and noncatalytic nucleotide binding sites of the Escherichia coli F1 ATPase Amino acid sequences of β‐subunit tryptic peptides labeled with 2‐azido‐ATP

P. Boyer, B. Hicke, J. Wise, 1987, FEBS letters.

Inhibition of BCRP in Multidrug Resistant Cancer using Novel Inhibitors

P. Vogel, J. Wise, Chanyang Park, 2020, The FASEB Journal.

Multiple Drug Transport Pathways through Human P-Glycoprotein.

P. Vogel, J. McCormick, J. Wise, 2015, Biochemistry.

On the location and function of tyrosine beta 331 in the catalytic site of Escherichia coli F1-ATPase.

J. Weber, A. E. Senior, R. Lee, 1992, The Journal of biological chemistry.

Site-directed mutagenesis of the conserved beta subunit tyrosine 331 of Escherichia coli ATP synthase yields catalytically active enzymes.

J G Wise, J. Wise, 1990, The Journal of biological chemistry.