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1.
Protein Sci ; 33(10): e5162, 2024 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-39276004

RESUMO

Jumonji-C (JmjC) domain-containing protein 7 (JMJD7) is a human Fe(II) and 2-oxoglutarate dependent oxygenase that catalyzes stereospecific C3-hydroxylation of lysyl-residues in developmentally regulated GTP binding proteins 1 and 2 (DRG1/2). We report studies exploring a diverse set of lysine derivatives incorporated into the DRG1 peptides as potential human JMJD7 substrates and inhibitors. The results indicate that human JMJD7 has a relatively narrow substrate scope beyond lysine compared to some other JmjC hydroxylases and lysine-modifying enzymes. The geometrically constrained (E)-dehydrolysine is an efficient alternative to lysine for JMJD7-catalyzed C3-hydroxylation. γ-Thialysine and γ-azalysine undergo C3-hydroxylation, followed by degradation to formylglycine. JMJD7 also catalyzes the S-oxidation of DRG1-derived peptides possessing methionine and homomethionine residues in place of lysine. Inhibition assays show that DRG1 variants possessing cysteine/selenocysteine instead of the lysine residue efficiently inhibit JMJD7 via cross-linking. The overall results inform on the substrate selectivity and inhibition of human JMJD7, which will help enable the rational design of selective small-molecule and peptidomimetic inhibitors of JMJD7.


Assuntos
Histona Desmetilases com o Domínio Jumonji , Humanos , Histona Desmetilases com o Domínio Jumonji/química , Histona Desmetilases com o Domínio Jumonji/metabolismo , Histona Desmetilases com o Domínio Jumonji/antagonistas & inibidores , Histona Desmetilases com o Domínio Jumonji/genética , Especificidade por Substrato , Lisina/química , Lisina/metabolismo , Inibidores Enzimáticos/química , Inibidores Enzimáticos/farmacologia , Hidroxilação
2.
J Biol Chem ; 300(8): 107546, 2024 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-38992435

RESUMO

In seeding plants, biosynthesis of the phytohormone ethylene, which regulates processes including fruit ripening and senescence, is catalyzed by 1-aminocyclopropane-1-carboxylic acid (ACC) oxidase. The plant pathogen Pseudomonas savastanoi (previously classified as: Pseudomonas syringae) employs a different type of ethylene-forming enzyme (psEFE), though from the same structural superfamily as ACC oxidase, to catalyze ethylene formation from 2-oxoglutarate (2OG) in an arginine dependent manner. psEFE also catalyzes the more typical oxidation of arginine to give L-Δ1-pyrroline-5-carboxylate (P5C), a reaction coupled to oxidative decarboxylation of 2OG giving succinate and CO2. We report on the effects of C3 and/or C4 substituted 2OG derivatives on the reaction modes of psEFE. 1H NMR assays, including using the pure shift method, reveal that, within our limits of detection, none of the tested 2OG derivatives is converted to an alkene; some are converted to the corresponding ß-hydroxypropionate or succinate derivatives, with only the latter being coupled to arginine oxidation. The NMR results reveal that the nature of 2OG derivatization can affect the outcome of the bifurcating reaction, with some 2OG derivatives exclusively favoring the arginine oxidation pathway. Given that some of the tested 2OG derivatives are natural products, the results are of potential biological relevance. There are also opportunities for therapeutic or biocatalytic regulation of the outcomes of reactions catalyzed by 2OG-dependent oxygenases by the use of 2OG derivatives.


Assuntos
Proteínas de Bactérias , Etilenos , Ácidos Cetoglutáricos , Pseudomonas , Pseudomonas/enzimologia , Pseudomonas/metabolismo , Ácidos Cetoglutáricos/metabolismo , Ácidos Cetoglutáricos/química , Etilenos/metabolismo , Etilenos/química , Proteínas de Bactérias/metabolismo , Proteínas de Bactérias/química , Proteínas de Bactérias/genética , Liases/metabolismo , Liases/química , Liases/genética , Arginina/metabolismo , Arginina/química , Oxirredução
3.
Mater Today Proc ; 56: 3740-3746, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35070729

RESUMO

The covid-19 pandemic has created problems in every manufacturing sector and has posed considerable challenges to pharmaceutical, healthcare, and sanitation companies. The challenges faced are particularly daunting for pharmaceutical companies producing vaccines with ever-growing demand and shorter and shorter deadlines to fulfill them. Further, due to the vaccine's novelty and unprecedented demand, there is a lack of any available data on which traditional forecasting methods can be used. In this paper, we attempt to propose a solution by utilizing the Grey Systems Theory, particularly the AGM (1, 1) model, which has been used to significant effect for problems involving uncertain / lack of data to forecast the demand for vaccines. The experimental results obtained showed that our proposed model successfully generated accurate forecasts with a small dataset and minimal error. Additionally, judgmental forecasting has been used to qualitatively assess the future scope of vaccine manufacturing as well as the use cases of the model. We can thus effectively say proposed AGM (1,1) model is a lucid method to forecast the demand for vaccines.

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