Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Gretchen Guaglianone"'
Autor:
Adam G. Kreutzer, Chelsea Marie T. Parrocha, Sepehr Haerianardakani, Gretchen Guaglianone, Jennifer T. Nguyen, Michelle N. Diab, William Yong, Mari Perez-Rosendahl, Elizabeth Head, James S. Nowick
Publikováno v:
ACS Central Science, Vol 10, Iss 1, Pp 104-121 (2023)
Externí odkaz:
https://doaj.org/article/098b29bada2f49a389917a993817e744
Autor:
Adam G. Kreutzer, Gretchen Guaglianone, Stan Yoo, Chelsea Marie T. Parrocha, Sarah M. Ruttenberg, Ryan J. Malonis, Karen Tong, Yu-Fu Lin, Jennifer T. Nguyen, William J. Howitz, Michelle N. Diab, Imane L. Hamza, Jonathan R. Lai, Vicki H. Wysocki, James S. Nowick
Publikováno v:
Proceedings of the National Academy of Sciences. 120
The assembly of the β-amyloid peptide (Aβ) to form oligomers and fibrils is closely associated with the pathogenesis and progression of Alzheimer’s disease. Aβ is a shape-shifting peptide capable of adopting many conformations and folds within t
Autor:
William J. Howitz, Gretchen Guaglianone, Kate J. McKnelly, Katelyn Haduong, Shareen N. Ashby, Mohamed Laayouni, James S. Nowick
Publikováno v:
ACS Chem Neurosci
This work probes the role of charge in the oligomeric assembly, toxicity, and membrane destabilization of a series of peptides derived from Aβ and the E22Q and E22K familial mutants. In the mutant Aβ peptides, an acidic residue (E) is replaced with
Autor:
Gretchen Guaglianone, Belén Torrado, Yu-Fu Lin, Matthew C. Watkins, Vicki H. Wysocki, Enrico Gratton, James S. Nowick
Publikováno v:
ACS chemical neuroscience, vol 13, iss 16
Aβ oligomers play a central role in the neurodegeneration observed with Alzheimer's disease. Our laboratory has developed covalently stabilized trimers derived from residues 17-36 of Aβ as model systems for studying Aβ oligomers. In the current st
Publikováno v:
Chemical science. 13(44)
The antibiotic teixobactin is a promising drug candidate against drug-resistant pathogens, such as MRSA and VRE, but forms insoluble gels that may limit intravenous administration.
Autor:
Adam G. Kreutzer, Tuan D. Samdin, Sepehr Haerianardakani, James S. Nowick, Patrick J. Salveson, Gretchen Guaglianone
Publikováno v:
J Am Chem Soc
Oligomers of the β-amyloid peptide, Aβ, play a central role in the pathogenesis and progression of Alzheimer’s disease. Trimers and higher-order oligomers composed of trimers are thought to be the most neurotoxic Aβ oligomers. To gain insights i
Autor:
Stan Yoo, James S. Nowick, William J. Howitz, Jonathan Lin, Li Xing, Adam G. Kreutzer, Grace Huizar, Michael A. Morris, Hannah Jusuf, Sheng Zhang, Jian-Guo Zheng, Gretchen Guaglianone
Publikováno v:
Biochemistry
Fluorescent derivatives of the β-amyloid peptides (Aβ) are valuable tools for studying the interactions of Aβ with cells. Facile access to labeled expressed Aβ offers the promise of Aβ with greater sequence and stereochemical integrity, without
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9989b1e5854bfdcca654482fa3733888
https://europepmc.org/articles/PMC9059633/
https://europepmc.org/articles/PMC9059633/
Autor:
Michael A. Morris, Chelsea Marie T. Parrocha, Carter T. Butts, Maj Krumberger, Gretchen Guaglianone, Adam G. Kreutzer, James S. Nowick, Elizabeth M. Diessner
Publikováno v:
European Journal of Medicinal Chemistry
This paper presents the design and study of a first-in-class cyclic peptide inhibitor against the SARS-CoV-2 main protease (Mpro). The cyclic peptide inhibitor is designed to mimic the conformation of a substrate at a C-terminal autolytic cleavage si
Autor:
Stan Yoo, Michael A. Morris, James S. Nowick, William J. Howitz, Jonathan Lin, Adam G. Kreutzer, Gretchen Guaglianone, Hannah Jusuf, Li Xing, Jian-Guo Zheng, Sheng Zhang, Grace Huizar
Publikováno v:
Biochemistry. 60:2272-2273
Autor:
Gretchen Guaglianone, Maj Krumberger, James S. Nowick, Chelsea Marie T. Parrocha, Adam G. Kreutzer, Michael A. Morris
This paper presents the design and study of a first-in-class cyclic peptide inhibitor against the SARS-CoV-2 main protease (Mpro). The cyclic peptide inhibitor is designed to mimic the conformation of a substrate at a C-terminal autolytic cleavage si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e4b35a8cef53b4f43528c14ed2b9222
https://doi.org/10.1101/2020.08.03.234872
https://doi.org/10.1101/2020.08.03.234872