Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Chaitanya Kumar Thota"'
Autor:
Chaitanya Kumar Thota, Allison A. Berger, Laura Elomaa, Chaunxiong Nie, Christoph Böttcher, Beate Koksch
Publikováno v:
ACS Omega, Vol 5, Iss 15, Pp 8557-8563 (2020)
Externí odkaz:
https://doaj.org/article/f263560b24d74936bf21dd559061a07b
Autor:
Sunil Bansal, Indresh Kumar Maurya, Nitin Yadav, Chaitanya Kumar Thota, Vinod Kumar, Kulbhushan Tikoo, Virander Singh Chauhan, Rahul Jain
Publikováno v:
ACS Omega, Vol 3, Iss 8, Pp 10019-10032 (2018)
Externí odkaz:
https://doaj.org/article/ce44b096da8c4802937c7c3fdef02295
Publikováno v:
ACS Med Chem Lett
[Image: see text] Antibiotic-resistant microbes have become a global health threat. New delivery systems that enhance the efficacy of antibiotics and/or overcome the resistances can help combat them. In this context, we present FF03, a fibril-forming
Autor:
Beate Koksch, Hans von Berlepsch, Maria Seidel, Chaitanya Kumar Thota, Christian Roth, Chaunxiong Xie, Roderich D. Süssmuth, Björn Harms, Christoph Böttcher, Allison Ann Berger
Publikováno v:
Peptide Sciences
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::675076e82da1df72b50217ccf719c035
https://hdl.handle.net/21.11116/0000-0004-6958-421.11116/0000-0005-A35B-D
https://hdl.handle.net/21.11116/0000-0004-6958-421.11116/0000-0005-A35B-D
Autor:
Chaitanya Kumar, Thota, Allison A, Berger, Laura, Elomaa, Chaunxiong, Nie, Christoph, Böttcher, Beate, Koksch
Publikováno v:
ACS Omega, Vol 5, Iss 15, Pp 8557-8563 (2020)
ACS Omega
ACS Omega
Multicomponent self-assembly of peptides is a powerful strategy to fabricate novel functional materials with synergetic properties that can be used for several nanobiotechnological applications. In the present study, we used a coassembly strategy to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30f9a5e4c98d660190d17a84374324d5
Autor:
Kulbhushan Tikoo, Sunil Bansal, Chaitanya Kumar Thota, Indresh Kumar Maurya, Nitin Yadav, Rahul Jain, Vinod Kumar, Virander S. Chauhan
Publikováno v:
ACS Omega, Vol 3, Iss 8, Pp 10019-10032 (2018)
ACS Omega
ACS Omega
Since the introduction of acetyl cholinesterase inhibitors as the first approved drugs by the US Food and Drug Administration for Alzheimer’s disease (AD) in clinics, less than satisfactory success in the design of anti-AD agents has impelled the s
Autor:
Nitin Yadav, Indresh Kumar Maurya, Chaitanya Kumar Thota, Sunil Bansal, Kulbhushan Tikoo, Kitika Shenmar, Rahul Jain, Vinod Kumar, Virander S. Chauhan
Publikováno v:
RSC Advances. 7:4167-4173
In an attempt to design Aβ aggregation inhibitors to combat Alzheimer's disease, herein we report a full peptide scan performed on a pentapeptide fragment (Aβ38–42) derived from the C-terminus of Aβ1–42 peptide. More than thirty new peptides w
Autor:
Rajendra Prasad, Virander S. Chauhan, Sobhan Sen, Andrew M. Lynn, Neeraj Chauhan, Jyotsna Sharma, Chaitanya Kumar Thota, Indresh Kumar Maurya, Manpreet Kaur Rawal, Sachin Dev Verma, Balaguru Ravikumar
Publikováno v:
Journal of Biological Chemistry. 295:3393
Drug-resistant pathogenic fungi use several families of membrane-embedded transporters to efflux antifungal drugs from the cells. The efflux pump Cdr1 (Candida drug resistance 1) belongs to the ATP-binding cassette (ABC) superfamily of transporters.
Autor:
Indresh Kumar Maurya, Indu Shekhar Thakur, Mukund V. Deshpande, Preeti M. Chaudhary, Jyotsna Sharma, Chaitanya Kumar Thota, Rajendra Prasad, Manoj Kumar Singh, Santosh G. Tupe, Virander S. Chauhan
Publikováno v:
Biochimica et Biophysica Acta (BBA) - General Subjects. 1830:5193-5203
Background Three de novo designed low molecular weight cationic peptides (IJ2, IJ3 and IJ4) containing an unnatural amino acid α,β-didehydrophenylalanine (∆Phe) exhibited potent antifungal activity against fluconazole (FLC) sensitive and resistan
Publikováno v:
Scientific Reports
Nanostructures including hydrogels based on peptides containing non protein amino acids are being considered as platform for drug delivery because of their inherent biocompatibility and additional proteolytic stability. Here we describe instantaneous