Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Joshua A. Kritzer"'
Autor:
Hawley Brown, Mia Chung, Alina Üffing, Nefeli Batistatou, Tiffany Tsang, Samantha Doskocil, Weiqun Mao, Dieter Willbold, Robert C. Bast, Zhen Lu, Oliver H. Weiergräber, Joshua A. Kritzer
Publikováno v:
Journal of the American Chemical Society. 144(32)
The LC3/GABARAP family of proteins is involved in nearly every stage of autophagy. Inhibition of LC3/GABARAP proteins is a promising approach to blocking autophagy, which sensitizes advanced cancers to DNA-damaging chemotherapy. Here, we report the s
Autor:
Nefeli Batistatou, Joshua A. Kritzer
Publikováno v:
ChemBioChem. 24
Autor:
Charles Abakah, Jiayuan Miao, Kirsten Deprey, James D. Baleja, Adam Moyer, Bryan J. Lampkin, Jennifer R. Pace, David Baker, Yu-Shan Lin, Joshua A. Kritzer, Robert A. Cerulli
Publikováno v:
J Am Chem Soc
Peptides constrained by intramolecular cross-links, especially stapled α-helices, have emerged as versatile scaffolds for drug development. However, there are fewer examples of similarly constrained scaffolds for other secondary structures. Here, we
Publikováno v:
ACS Chem Biol
The efficiency with which polycationic peptides penetrate the cytosol depends on the number and overall patterning of arginine residues. While general trends and unusually penetrant patterns of arginine residues have been discovered, prior work has n
Publikováno v:
Nucleic Acids Research
RNA therapeutics are a promising strategy to treat genetic diseases caused by the overexpression or aberrant splicing of a specific protein. The field has seen major strides in the clinical efficacy of this class of molecules, largely due to chemical
Autor:
Joshua A. Kritzer, Jennifer R. Pace, Hawley F. Brown, Robert A. Cerulli, Livia Shehaj, Yang Mei
Publikováno v:
Chembiochem
A growing body of evidence suggests that autophagy inhibition enhances the effectiveness of chemotherapy, especially in difficult-to-treat cancers. Existing autophagy inhibitors are primarily lysosomotropic agents. More specific autophagy inhibitors
Autor:
Joshua A. Kritzer, Robert A. Cerulli
Publikováno v:
Org Biomol Chem
Tyrosine phosphorylation is a critical component of signal transduction for multicellular organisms, particularly for pathways that regulate cell proliferation and differentiation. While tyrosine kinase inhibitors have become FDA-approved drugs, inhi
Autor:
Kirsten Deprey, Nefeli Batistatou, Marjoke F. Debets, Jack Godfrey, Kirstin B. VanderWall, Rebecca R. Miles, Livia Shehaj, Jiaxing Guo, Amy Andreucci, Pachamuthu Kandasamy, Genliang Lu, Mamoru Shimizu, Chandra Vargeese, Joshua A. Kritzer
Publikováno v:
ACS Chem Biol
A major obstacle to the development of effective oligonucleotide therapeutics is a lack of understanding about their cytosolic and nuclear penetration. To address this problem, we have applied the chloroalkane penetration assay (CAPA) to oligonucleot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ca7a1a52699e0b7e5fa1b2efc41faf6
https://europepmc.org/articles/PMC9252293/
https://europepmc.org/articles/PMC9252293/
Autor:
Seth T. Gammon, Jing Wang, Hailing Yang, Philip Rask, Robert C. Bast, Margie N. Sutton, Joshua A. Kritzer, David Piwnica-Worms, Zhen Lu, Brian J. Engel, Joshua P. Gray, Nasir Uddin, Brian J. Grindel, Shuxing Zhang, Hannah Locke, Pratip K. Bhattacharya, Nefeli Batistatou, Rajan Chaudhari, Steven W. Millward
Publikováno v:
Chemical Science
In recent decades it has become increasingly clear that induction of autophagy plays an important role in the development of treatment resistance and dormancy in many cancer types. Unfortunately, chloroquine (CQ) and hydroxychloroquine (HCQ), two aut
Autor:
Joshua A. Kritzer, Yu-Shan Lin, Jiayuan Miao, Diana P. Slough, Sean M. McHugh, Ashleigh E. Cummings
Publikováno v:
Biophysical Journal. 116:433-444
Cyclic peptides (CPs) are a promising class of molecules for drug development, particularly as inhibitors of protein-protein interactions. Predicting low-energy structures and global structural ensembles of individual CPs is critical for the design o