A short peptide from sAPPα binding to BACE1-APP action site rescues Alzheimer-like pathology

2021 ◽  
pp. 136397
Author(s):  
Xia Lai ◽  
Jie Hu ◽  
He Liu ◽  
Ling Lan ◽  
Yan Long ◽  
...  
Keyword(s):  
Author(s):  
Sha Lin ◽  
Hui Sun ◽  
Erik Jan Cornel ◽  
Jin-Hui Jiang ◽  
Yun-Qing Zhu ◽  
...  
Keyword(s):  

Molecules ◽  
2021 ◽  
Vol 26 (2) ◽  
pp. 430
Author(s):  
Vasso Apostolopoulos ◽  
Joanna Bojarska ◽  
Tsun-Thai Chai ◽  
Sherif Elnagdy ◽  
Krzysztof Kaczmarek ◽  
...  

Peptides are fragments of proteins that carry out biological functions. They act as signaling entities via all domains of life and interfere with protein-protein interactions, which are indispensable in bio-processes. Short peptides include fundamental molecular information for a prelude to the symphony of life. They have aroused considerable interest due to their unique features and great promise in innovative bio-therapies. This work focusing on the current state-of-the-art short peptide-based therapeutical developments is the first global review written by researchers from all continents, as a celebration of 100 years of peptide therapeutics since the commencement of insulin therapy in the 1920s. Peptide “drugs” initially played only the role of hormone analogs to balance disorders. Nowadays, they achieve numerous biomedical tasks, can cross membranes, or reach intracellular targets. The role of peptides in bio-processes can hardly be mimicked by other chemical substances. The article is divided into independent sections, which are related to either the progress in short peptide-based theranostics or the problems posing challenge to bio-medicine. In particular, the SWOT analysis of short peptides, their relevance in therapies of diverse diseases, improvements in (bio)synthesis platforms, advanced nano-supramolecular technologies, aptamers, altered peptide ligands and in silico methodologies to overcome peptide limitations, modern smart bio-functional materials, vaccines, and drug/gene-targeted delivery systems are discussed.


2011 ◽  
Vol 54 (13) ◽  
pp. 4627-4637 ◽  
Author(s):  
Philippe Wolff ◽  
Vincent Oliéric ◽  
Jean Paul Briand ◽  
Olivier Chaloin ◽  
Annick Dejaegere ◽  
...  

2005 ◽  
Vol 102 (44) ◽  
pp. 15815-15820 ◽  
Author(s):  
J. Yin ◽  
P. D. Straight ◽  
S. M. McLoughlin ◽  
Z. Zhou ◽  
A. J. Lin ◽  
...  

2017 ◽  
Vol 44 (9) ◽  
pp. 1325-1342 ◽  
Author(s):  
Aneta M. Białkowska ◽  
Krzysztof Morawski ◽  
Tomasz Florczak

2021 ◽  
Author(s):  
Luhan Zhai ◽  
Masayuki Nara ◽  
Yuko Otani ◽  
Tomohiko Ohwada

NH-π and CH-π interactions, due to its weak character, are not easily to be identified in solution. We report a group of isolable short peptides with stable folds, in which...


Molecules ◽  
2019 ◽  
Vol 24 (3) ◽  
pp. 405 ◽  
Author(s):  
Brett H. Pogostin ◽  
Anders Malmendal ◽  
Casey H. Londergan ◽  
Karin S. Åkerfeldt

Determining the pKa of key functional groups is critical to understanding the pH-dependent behavior of biological proteins and peptide-based biomaterials. Traditionally, 1H NMR spectroscopy has been used to determine the pKa of amino acids; however, for larger molecules and aggregating systems, this method can be practically impossible. Previous studies concluded that the C-D stretches in Raman are a useful alternative for determining the pKa of histidine residues. In this study, we report on the Raman application of the C2-D probe on histidine’s imidazole side chain to determining the pKa of histidine in a short peptide sequence. The pKa of the tripeptide was found via difference Raman spectroscopy to be 6.82, and this value was independently confirmed via 1H NMR spectroscopy on the same peptide. The C2-D probe was also compared to other Raman reporters of the protonation state of histidine and was determined to be more sensitive and reliable than other protonation-dependent signals. The C2-D Raman probe expands the tool box available to chemists interested in directly interrogating the pKa’s of histidine-containing peptide and protein systems.


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