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1.
BMC Bioinformatics ; 25(1): 156, 2024 Apr 20.
Article in English | MEDLINE | ID: mdl-38641811

ABSTRACT

BACKGROUND: Accurately identifying drug-target interaction (DTI), affinity (DTA), and binding sites (DTS) is crucial for drug screening, repositioning, and design, as well as for understanding the functions of target. Although there are a few online platforms based on deep learning for drug-target interaction, affinity, and binding sites identification, there is currently no integrated online platforms for all three aspects. RESULTS: Our solution, the novel integrated online platform Drug-Online, has been developed to facilitate drug screening, target identification, and understanding the functions of target in a progressive manner of "interaction-affinity-binding sites". Drug-Online platform consists of three parts: the first part uses the drug-target interaction identification method MGraphDTA, based on graph neural networks (GNN) and convolutional neural networks (CNN), to identify whether there is a drug-target interaction. If an interaction is identified, the second part employs the drug-target affinity identification method MMDTA, also based on GNN and CNN, to calculate the strength of drug-target interaction, i.e., affinity. Finally, the third part identifies drug-target binding sites, i.e., pockets. The method pt-lm-gnn used in this part is also based on GNN. CONCLUSIONS: Drug-Online is a reliable online platform that integrates drug-target interaction, affinity, and binding sites identification. It is freely available via the Internet at http://39.106.7.26:8000/Drug-Online/ .


Subject(s)
Deep Learning , Drug Interactions , Binding Sites , Drug Delivery Systems , Drug Evaluation, Preclinical
2.
Int Heart J ; 65(2): 173-179, 2024.
Article in English | MEDLINE | ID: mdl-38556328

ABSTRACT

Keshan disease (KD) is a type of endemic cardiomyopathy with an unknown cause. It is primarily found in areas in China with low selenium levels, from northeast to southwest. The nutritional biogeochemical etiology hypothesis suggests that selenium deficiency is a major factor in KD development. Selenium is important in removing free radicals and protecting cells and tissues from peroxide-induced damage. Thus, low environmental selenium may affect the selenium level within the human body, and selenium level differences are commonly observed between healthy people in KD and nonKD areas. From the 1970s to the 1990s, China successfully reduced KD incidence in endemic KD areas through a selenium supplementation program. After years of implementing prevention and control measures, the selenium level of the population in the KD areas has gradually increased, and the prevalence of KD in China has remained low and stable in recent years. Currently, the pathogenesis of KD remains vague, and the effect of selenium supplementation on the prognosis of KD still needs further study. This paper comprehensively reviews selenium deficiency and its connection to KD. Thus, this study aims to offer novel ideas and directions to effectively prevent and treat KD in light of the current situation.


Subject(s)
Cardiomyopathies , Enterovirus Infections , Malnutrition , Selenium , Humans , Selenium/analysis , Cardiomyopathies/epidemiology , Cardiomyopathies/etiology , Cardiomyopathies/prevention & control , Enterovirus Infections/complications , Enterovirus Infections/epidemiology , Enterovirus Infections/prevention & control , China/epidemiology
3.
Carbohydr Polym ; 256: 117556, 2021 Mar 15.
Article in English | MEDLINE | ID: mdl-33483059

ABSTRACT

Acute kidney injury (AKI) is a common and serious clinical syndrome of acute renal dysfunction in a short period. One of therapeutic interventions for AKI is to reduce ROS massively generated in the mitochondria and then ameliorate cell damage and apoptosis induced by oxidative stress. In this study, stepwise-targeting chitosan oligosaccharide, triphenyl phosphine-low molecular weight chitosan-curcumin (TPP-LMWC-CUR, TLC), was constructed for sepsis-induced AKI via removing excessive ROS in renal tubular epithelial cells. Benefiting from good water solubility and low molecular weight, TLC was rapidly and preferentially distributed in the renal tissues and then specifically internalized by tubular epithelium cells via interaction between Megalin receptor and LMWC. The intracellular TLC could further delivery CUR to mitochondria due to high buffering capacity of LMWC and delocalized positive charges of TPP. Both in vitro and in vivo pharmacodynamic results demonstrated the enhanced therapeutic effect of TLC in the treatment of AKI.


Subject(s)
Acute Kidney Injury/drug therapy , Chitosan/chemistry , Kidney Tubules/drug effects , Oligosaccharides/chemistry , Animals , Apoptosis , Buffers , Cell Line , Cell Survival , Drug Delivery Systems , Endocytosis , Epithelium/drug effects , Humans , In Vitro Techniques , Inflammation , Kidney/metabolism , Low Density Lipoprotein Receptor-Related Protein-2/metabolism , Lysosomes/metabolism , Male , Mice , Mice, Inbred BALB C , Mitochondria/drug effects , Oxidative Stress , Polymers/chemistry , Reactive Oxygen Species , Solubility , Spectrometry, Fluorescence
4.
Article in Chinese | MEDLINE | ID: mdl-16622314

ABSTRACT

In this study, betA gene was introduced into the pollen plantlets of Populus simonii x P. nigra using Agrobacterium-mediated transformation. The four kanamycine-resistant plants obtained were identified as transgenic plants by PCR detection and the results were all positive. The result of quantitative real-time PCR detection showed that the betA gene was transcribed and expressed in all the transformed plants, but the transcript levels are different. Test of salt-tolerance of the transgenic plants showed that 80%-00% of transgenic plants were rooted while 0 of non-transgenic plants were rooted at 0.55% NaCl stress, and 0 of transgenic plants were rooted at 0.70%-0.80% NaCl stress. The betaine content analysis showed the betaine content of the transgenic plants are obviously higher than that in non-transgenic plants, so transformation betA gene raised the salt tolerance to the transgenic plants.


Subject(s)
Choline Dehydrogenase/genetics , Plants, Genetically Modified/genetics , Pollen/genetics , Populus/genetics , Betaine/metabolism , Choline Dehydrogenase/metabolism , Gene Expression Regulation, Plant/drug effects , Plants, Genetically Modified/drug effects , Plants, Genetically Modified/metabolism , Pollen/cytology , Populus/drug effects , Populus/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Rhizobium/genetics , Sodium Chloride/pharmacology , Transformation, Genetic
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