Exploring the potential of amyloids in biomedical applications: A review
S Chowdhury, N Sarkar - Biotechnology and Bioengineering, 2024 - Wiley Online Library
Amyloid is defined as a fibrous quaternary structure formed by assembling protein or peptide
monomers into intermolecularly hydrogen linked β‐sheets. There is a prevalent issue with …
monomers into intermolecularly hydrogen linked β‐sheets. There is a prevalent issue with …
Advances in protein misfolding, amyloidosis and its correlation with human diseases
Protein aggregation, their mechanisms and trends in the field of neurodegenerative
diseases is still far from completely being decoded. It is mainly attributed to the complexity …
diseases is still far from completely being decoded. It is mainly attributed to the complexity …
Proline functionalized gold nanoparticles modulates lysozyme fibrillation
Amyloid fibrils are the hallmarks of neurodegenerative diseases like Alzheimer's,
Parkinson's and other proteopathies. Inhibition of fibrillation is a potential strategy to check …
Parkinson's and other proteopathies. Inhibition of fibrillation is a potential strategy to check …
Elucidating the inhibitory effects of rationally designed novel hexapeptide against hen egg white lysozyme fibrillation at acidic and physiological pH
Inhibition of highly ordered cross-β-sheet-rich aggregates of misfolded amyloid proteins
using rationally designed sequence-based short peptides is a promising therapeutic …
using rationally designed sequence-based short peptides is a promising therapeutic …
Rottlerin dissolves pre-formed protein amyloid: A study on hen egg white lysozyme
BACKGROUND: Deposition of protein fibrillar aggregates called amyloids in the tissue, is
the principal cause of several degenerative diseases. Here, we have shown the …
the principal cause of several degenerative diseases. Here, we have shown the …
Exploring critical determinants of protein amyloidogenesis: a review
The transformation of polypeptide chains from their globular native structure to fibrillar
aggregates has been a matter of great concern because of the involvement of these …
aggregates has been a matter of great concern because of the involvement of these …
Biochemical properties and aggregation propensity of transforming growth factor-induced protein (TGFBIp) and the amyloid forming mutants
R Lakshminarayanan, SS Chaurasia, E Murugan… - The ocular …, 2015 - Elsevier
TGFBI-associated corneal dystrophies are characterized by accumulation of insoluble
deposits of the mutant protein transforming growth factor β− induced protein (TGFBIp) in the …
deposits of the mutant protein transforming growth factor β− induced protein (TGFBIp) in the …
Carboxylic Group Functionalized Carbon Quantum Dots inhibit Hen Egg White Lysozyme Amyloidogenesis, leading to the Formation of Spherical Aggregates with …
MPT Prabhu, S Chrungoo… - Current Protein and …, 2024 - benthamdirect.com
Introduction: Proteinopathies are a group of diseases where the protein structure has been
altered. These alterations are linked to the production of amyloids, which are persistent …
altered. These alterations are linked to the production of amyloids, which are persistent …
Insight into the co-solvent induced conformational changes and aggregation of bovine β-lactoglobulin
S Pal, S Maity, S Sardar, J Chakraborty… - International journal of …, 2016 - Elsevier
Many proteins form ordered irreversible aggregates called amyloid fibrils which are
responsible for several neurodegenerative diseases. β-lactoglobulin (β-lg), an important …
responsible for several neurodegenerative diseases. β-lactoglobulin (β-lg), an important …
Exploring possibility of promiscuity of amyloid inhibitor: Studies on effect of selected compounds on folding and amyloid formation of proteins
Fibrillar protein aggregates called amyloids are the hallmark of several degenerative
diseases. Identification of common drugs which are capable of blocking or inhibiting protein …
diseases. Identification of common drugs which are capable of blocking or inhibiting protein …