نتایج جستجو برای: chemical chaperone

تعداد نتایج: 390727  

2015
Sandip Kumar Nandi Ayon Chakraborty Alok Kumar Panda Sougata Sinha Ray Rajiv Kumar Kar Anirban Bhunia Ashis Biswas

Adenosine-5'-triphosphate (ATP) is an important phosphate metabolite abundantly found in Mycobacterium leprae bacilli. This pathogen does not derive ATP from its host but has its own mechanism for the generation of ATP. Interestingly, this molecule as well as several antigenic proteins act as bio-markers for the detection of leprosy. One such bio-marker is the 18 kDa antigen. This 18 kDa antige...

2013
Alex Dickson Charles L. Brooks

For cells to function, the concentrations of all proteins in the cell must be maintained at the proper levels (proteostasis). This task--complicated by cellular stresses, protein misfolding, aggregation, and degradation--is performed by a collection of chaperones that alter the configurational landscape of a given client protein through the formation of protein-chaperone complexes. The set of a...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2006
Jerome S Pinkner Han Remaut Floris Buelens Eric Miller Veronica Aberg Nils Pemberton Mattias Hedenström Andreas Larsson Patrick Seed Gabriel Waksman Scott J Hultgren Fredrik Almqvist

A chemical synthesis platform with broad applications and flexibility was rationally designed to inhibit biogenesis of adhesive pili assembled by the chaperone-usher pathway in Gram-negative pathogens. The activity of a family of bicyclic 2-pyridones, termed pilicides, was evaluated in two different pilus biogenesis systems in uropathogenic Escherichia coli. Hemagglutination mediated by either ...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2009
Umesh K Jinwal Yoshinari Miyata John Koren Jeffrey R Jones Justin H Trotter Lyra Chang John O'Leary David Morgan Daniel C Lee Cody L Shults Aikaterini Rousaki Edwin J Weeber Erik R P Zuiderweg Jason E Gestwicki Chad A Dickey

Alzheimer's disease and other tauopathies have recently been clustered with a group of nervous system disorders termed protein misfolding diseases. The common element established between these disorders is their requirement for processing by the chaperone complex. It is now clear that the individual components of the chaperone system, such as Hsp70 and Hsp90, exist in an intricate signaling net...

2017
Megan Garvey Heath Ecroyd Nicholas J. Ray Juliet A. Gerrard John A. Carver

Amyloid fibril formation occurs from a wide range of peptides and proteins and is typically associated with a loss of protein function and/or a gain of toxic function, as the native structure of the protein undergoes major alteration to form a cross β-sheet array. It is now well recognised that some amyloid fibrils have a biological function, which has led to increased interest in the potential...

Journal: :Biochimie 2005
Chuan-Peng Liu Zhen-Yu Li Guo-Chang Huang Sarah Perrett Jun-Mei Zhou

Trigger factor (TF) is an important catalyst of nascent peptide folding and possesses both peptidyl-prolyl cis-trans isomerase (PPIase) and chaperone activities. TF has a modular structure, containing three domains with distinct structural and functional properties. The guanidine hydrochloride (GuHCl) induced unfolding of TF was investigated by monitoring Trp fluorescence, far-UV CD, second-der...

2013
Sergey Lupachyk Pierre Watcho Roman Stavniichuk Hanna Shevalye Irina G. Obrosova

Endoplasmic reticulum stress resulting from abnormal folding of newly synthesized proteins impairs metabolism, transcriptional regulation, and gene expression, and it is a key mechanism of cell injury. Endoplasmic reticulum stress plays an important role in cardiovascular and neurodegenerative diseases, cancer, and diabetes. We evaluated the role for this phenomenon in diabetic peripheral neuro...

2013
Aaron Carman Sarah Kishinevsky John Koren Wenjie Lou Gabriela Chiosis

Maintenance of cellular homeostasis is regulated by the molecular chaperones. Under pathogenic conditions, aberrant proteins are triaged by the chaperone network. These aberrant proteins, known as "clients," have major roles in the pathogenesis of numerous neurological disorders, including tau in Alzheimer's disease, α-synuclein and LRRK2 in Parkinson's disease, SOD-1, TDP-43 and FUS in amyotro...

2017
Melinda S Hanes Kelley W Moremen Richard D Cummings

Cosmc is an endoplasmic reticulum chaperone necessary for normal protein O-GalNAc glycosylation through regulation of T-synthase, its single client. Loss-of-function of Cosmc results in expression of the Tn antigen, which is associated with multiple human diseases including cancer. Despite intense interest in dysregulated expression of the Tn antigen, little is known about the structure and fun...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2015
Bora Inceoglu Ahmed Bettaieb Carlos A Trindade da Silva Kin Sing Stephen Lee Fawaz G Haj Bruce D Hammock

Despite intensive effort and resulting gains in understanding the mechanisms underlying neuropathic pain, limited success in therapeutic approaches have been attained. A recently identified, nonchannel, nonneurotransmitter therapeutic target for pain is the enzyme soluble epoxide hydrolase (sEH). The sEH degrades natural analgesic lipid mediators, epoxy fatty acids (EpFAs), therefore its inhibi...

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