نتایج جستجو برای: toxic peptides

تعداد نتایج: 154826  

2016
Hongbo Jiang Donghun Kim Sharon Dobesh Jay D. Evans Ronald J. Nachman Krzysztof Kaczmarek Janusz Zabrocki Yoonseong Park

The varroa mite, Varroa destructor, is a devastating ectoparasite of the honey bees Apis mellifera and A. cerana. Control of these mites in beehives is a challenge in part due to the lack of toxic agents that are specific to mites and not to the host honey bee. In searching for a specific toxic target of varroa mites, we investigated two closely related neuropeptidergic systems, tachykinin-rela...

Journal: :Human molecular genetics 2002
Wen Yang John R Dunlap Richard B Andrews Ronald Wetzel

A number of observations point to the aggregation of expanded polyglutamine [poly(Q)]-containing proteins as playing a central role in the etiology of Huntington's disease (HD) and other expanded CAG-repeat diseases. Transfected cell and transgenic animal models provide some of this support, but irrefutable data on the cytotoxicity of poly(Q) aggregates is lacking. This may be due in part to di...

2013
Nicola Acerra Neil M. Kad Jody M. Mason

Aggregation of the β-amyloid (Aβ) peptide into toxic oligomers is considered the primary event in the pathogenesis of Alzheimer's disease. Previously generated peptides and mimetics designed to bind to amyloid fibrils have encountered problems in solubility, protease susceptibility and the population of small soluble toxic oligomers. We present a new method that opens the possibility of derivin...

Journal: :Genomics 2006
Jian-Ping Yang Wufang Fan Cheryl Rogers Jon E Chatterton Joshua Bliesath Guohong Liu Ning Ke Cui-Ying Wang Kristina Rhoades Flossie Wong-Staal Qi-Xiang Li

Combinatorial gene inactivation using an RNAi library is a powerful approach to discovering novel functional genes. However, generation of a comprehensive RNAi library remains technically challenging. In this report, we describe a simple and novel approach to designing gene-family-specific RNAi libraries by targeting conserved motifs using degenerate oligonucleotides. We created an siRNA librar...

Journal: :American journal of veterinary research 1995
A Sahin F G Tencalla D R Dietrich K Mez H Naegeli

Microcystin and related toxic peptides produced by cyanobacteria (blue-green algae) are potent and selective inhibitors of protein phosphatases 1 and 2A. We adapted existing enzymatic techniques to analyze the liver of rainbow trout after oral administration of hepatotoxic cyanobacteria. Liver tissue was removed 3 and 12 hours after treatment, and phosphatase activity was determined in liver ex...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1997
C Hertel E Terzi N Hauser R Jakob-Rotne J Seelig J A Kemp

The accumulation of beta-amyloid peptides (Abeta) into senile plaques is one of the hallmarks of Alzheimer disease. Aggregated Abeta is toxic to cells in culture and this has been considered to be the cause of neurodegeneration that occurs in the Alzheimer disease brain. The discovery of compounds that prevent Abeta toxicity may lead to a better understanding of the processes involved and ultim...

Journal: :Antimicrobial agents and chemotherapy 2014
Mohamed F Mohamed Maha I Hamed Alyssa Panitch Mohamed N Seleem

The seriousness of microbial resistance combined with the lack of new antimicrobials has increased interest in the development of antimicrobial peptides (AMPs) as novel therapeutics. In this study, we evaluated the antimicrobial activities of two short synthetic peptides, namely, RRIKA and RR. These peptides exhibited potent antimicrobial activity against Staphylococcus aureus, and their antimi...

2016
Christina Dammers Deniz Yolcu Laura Kukuk Dieter Willbold Marcus Pickhardt Eckhard Mandelkow Anselm H. C. Horn Heinrich Sticht Marwa Nidal Malhis Nadja Will Judith Schuster Susanne Aileen Funke

A variety of neurodegenerative disorders, including Alzheimer disease (AD), are associated with neurofibrillary tangles composed of the tau protein, as well as toxic tau oligomers. Inhibitors of pathological tau aggregation, interrupting tau self-assembly, might be useful for the development of therapeutics. Employing mirror image phage display with a large peptide library (over 109 different p...

2016
Qian Xiao Bo Feng Wei Luo Lichun Sun

Traditional chemotherapeutic agents exhibit potent anticancer efficacy. However, in clinical applications, they also exhibit severely toxic side effects, and result in multidrug resistance (MDR) of cancer cells. So, receptor-targeted therapy is catching more attention of scientists from both academic and industry and recently is coming to the central stage of drug development. Certain peptides,...

2016
Qing Zhao Wanghui Xu Lei Xing Zhanglin Lin

BACKGROUND Peptides have recently become attractive for therapeutic applications. However, efficient production of medium- to large-sized peptides (30-100 amino acids [aa]) remains challenging both by recombinant and chemical synthesis. We previously reported the formation of active enzyme aggregates in Escherichia coli cells induced by the short β-structured peptide ELK16 (LELELKLKLELELKLK) an...

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