monica montero lomeli

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Universidade Federal do rio de Janeiro
Universidade Federal do rio de Janeiro

monica montero lomeli


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Scopus Publications

Scopus Publications

  • Galactose-1-phosphate inhibits cytochrome c oxidase and causes mitochondrial dysfunction in classic galactosemia
    Caio M. Machado, Eduardo de-Souza-Ferreira, Guilherme F.S. Silva, Felipe S.A. Pimentel, Evandro A. De-Souza, Thaia Silva-Rodrigues, Ana C.P. Gandara, Julianna D. Zeidler, Lorena O. Fernandes-Siqueira, Ana Luiza F.V. De-Queiroz, Letícia Andrade-Silva, Klara Victória-Martins, Clara Fernandes-Carvalho, Eduardo N. Chini, João F. Passos, Andrea T. Da Poian, Mónica Montero-Lomelí, Antonio Galina, Claudio A. Masuda
    Biochimica Et Biophysica Acta Molecular Basis of Disease, 2024
  • Development and assessment of a multiepitope synthetic antigen for the diagnosis of Dengue virus infection
    Isis Botelho Nunes da Silva, Juliano de Moraes Rodrigues, Ramon Cid Gismonti Batista, Vivian dos Santos Gomes, Clarissa de Souza Chacon, Marcius da Silva Almeida, Talita Stelling de Araujo, Bianca Ortiz da Silva, Terezinha Marta Pereira Pinto Castiñeiras, Orlando da Costa Ferreira Junior, Fabiana Avila Carneiro, Monica Montero-Lomeli
    Brazilian Journal of Infectious Diseases, 2024
    Immunodiagnostic tests for detecting dengue virus infections encounter challenges related to cross-reactivity with other related flaviviruses. Our research focuses on the development of a synthetic multiepitope antigen tailored for dengue immunodiagnostics. Selected dengue epitopes involved structural linearity and dissimilarity from the proteomes of Zika and Yellow fever viruses which served for computationally modeling the three-dimensional protein structure, resulting in the design of two proteins: rDME-C and rDME-BR. Both proteins consist of seven epitopes, separated by the GPGPG linker, and a carboxy-terminal 6 × -histidine tag. The molecular weights of the final proteins rDME-C and rDME-BR are 16.83 kDa and 16.80 kDa, respectively, both with an isoelectric point of 6.35. The distinguishing factor between the two proteins lies in the origin of their epitope sequences, where rDME-C is based on the reference dengue proteome, while rDME-BR utilizes sequences from prevalent Dengue genotypes in Brazil from 2008 to 2019. PyMol analysis revealed exposure of epitopes in the secondary structure. Successful expression of the antigens was achieved in soluble form and fluorescence experiments indicated a disordered structure. In subsequent testing, rDME-BR and rDME-C antigens were assessed using an indirect Elisa protocol against Dengue infected serum, previously examined with a commercial diagnostic test. Optimal concentrations for antigens were determined at 10 µg/mL for rDME-BR and 30 µg/mL for rDME-C, with serum dilutions ranging from 1:50 to 1:100. Both antigens effectively detected IgM and IgG antibodies in Dengue fever patients, with rDME-BR exhibiting higher sensitivity. Our in-house test showed a sensitivity of 77.3 % and 82.6 % and a specificity of 89.4 % and 71.4 % for rDME-C and rDEM-BR antigens. No cross-reactivity was observed with serum from Zika-infected mice but with COVID-19 serum samples. Our findings underscore the utility of synthetic biology in crafting Dengue-specific multiepitope proteins and hold promise for precise clinical diagnosis and monitoring responses to emerging Dengue vaccines.
  • Lipidome remodeling in response to nutrient replenishment requires the tRNA modifier Deg1/Pus3 in yeast
    Gabriel Soares Matos, Leonie Vogt, Rosangela Silva Santos, Aurélien Devillars, Marcos Yukio Yoshinaga, Sayuri Miyamoto, Raffael Schaffrath, Monica Montero‐Lomeli, Roland Klassen
    Molecular Microbiology, 2023
    In the yeast Saccharomyces cerevisiae, the absence of the pseudouridine synthase Pus3/Deg1, which modifies tRNA positions 38 and 39, results in increased lipid droplet (LD) content and translational defects. In addition, starvation‐like transcriptome alterations and induced protein aggregation were observed. In this study, we show that the deg1 mutant increases specific misreading errors. This could lead to altered expression of the main regulators of neutral lipid synthesis which are the acetyl‐CoA carboxylase (Acc1), an enzyme that catalyzes a key step in fatty acid synthesis, and its regulator, the Snf1/AMPK kinase. We demonstrate that upregulation of the neutral lipid content of LD in the deg1 mutant is achieved by a mechanism operating in parallel to the known Snf1/AMPK kinase‐dependent phosphoregulation of Acc1. While in wild‐type cells removal of the regulatory phosphorylation site (Ser‐1157) in Acc1 results in strong upregulation of triacylglycerol (TG), but not steryl esters (SE), the deg1 mutation more specifically upregulates SE levels. In order to elucidate if other lipid species are affected, we compared the lipidomes of wild type and deg1 mutants, revealing multiple altered lipid species. In particular, in the exponential phase of growth, the deg1 mutant shows a reduction in the pool of phospholipids, indicating a compromised capacity to mobilize acyl‐CoA from storage lipids. We conclude that Deg1 plays a key role in the coordination of lipid storage and mobilization, which in turn influences lipid homeostasis. The lipidomic effects in the deg1 mutant may be indirect outcomes of the activation of various stress responses resulting from protein aggregation.
  • Accuracy of a raw saliva-based COVID-19 RT-LAMP diagnostic assay
    Kátia Maria dos Santos Cabral, Ramon Cid Gismonti Baptista, Terezinha Marta Pereira Pinto Castineiras, Amilcar Tanuri, Fabiana Avila Carneiro, Marcius da Silva Almeida, Monica Montero-Lomeli
    Brazilian Journal of Infectious Diseases, 2023
    The Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) pandemic demanded rapid diagnosis to isolate new COVID-19 cases and prevent disease transmission. Quantitative Real-Time Polymerase Chain Reaction (qRT-PCR) rapidly became the gold standard for diagnosis. However, due to the high cost and delay of the results, other types of diagnosis were implemented, such as COVID-19 Ag Rapid Tests and Reverse Transcription Technique followed by Loop-Mediated isothermal Amplification (RT-LAMP). In this work, we validated the use of RT-LAMP in saliva samples rather than nasopharyngeal swabs, as the collection is more comfortable. First, we selected 5 primer sets based on the limit of detection for SARS-CoV-2 RNA, then validated their sensitivity and specificity in patient samples. A total of 117 samples were analyzed by fluorometric RT-LAMP and compared with qRT-PCR results. Our results show that the use of a high-sensitive primer ORF1-a, together with a low-sensitive primer set Gene E (time to threshold of 22.9 and 36.4 minutes, respectively, using 200 copies of viral RNA), achieved sensitivity in purified RNA from saliva samples of 95.2% (95% CI 76.1‒99.8) with 90.5% specificity (95% CI 69.6‒98.8) (n = 42).As RNA purification increases the turnaround time, we tested the outcome of RT-LAMP utilizing raw saliva samples without purification. The test achieved a sensitivity of 81.8% (95% CI 59.7‒94.8) and a specificity of 90.9% (95% CI 70.8‒98.8). As a result, the accuracy of 92.9% (95% CI 80.5‒98.5) in purified RNA-saliva samples was lowered to an acceptable level of 86.4% (95% CI 72.6‒94.8) in raw saliva. Although mass vaccination has been implemented, new strains and low vaccination progress helped to spread COVID-19. This study shows that it is feasible to track new COVID-19 cases in a large population with the use of raw saliva as sample in RT-LAMP assay which yields accurate results and offers a less invasive test.
  • Sphingolipid depletion suppresses UPR activation and promotes galactose hypersensitivity in yeast models of classic galactosemia
    Felipe S.A. Pimentel, Caio M. Machado, Evandro A. De-Souza, Caroline Mota Fernandes, Ana Luiza F.V. De-Queiroz, Guilherme F.S. Silva, Maurizio Del Poeta, Monica Montero-Lomeli, Claudio A. Masuda
    Biochimica Et Biophysica Acta Molecular Basis of Disease, 2022
  • Regulation of sphingolipid synthesis by the G1/S transcription factor Swi4
    Gabriel S. Matos, Juliana B. Madeira, Caroline Mota Fernandes, Deveney Dasilva, Claudio A. Masuda, Maurizio Del Poeta, Monica Montero-Lomelí
    Biochimica Et Biophysica Acta Molecular and Cell Biology of Lipids, 2021
  • The yeast protein Ubx4p contributes to mitochondrial respiration and lithium- galactose-mediated activation of the unfolded protein response
    Evandro A. De-Souza, Felipe S.A. Pimentel, Ana Luiza F.V. De-Queiroz, Henrique Camara, Mikaella L. Felix-Formiga, Caio M. Machado, Silas Pinto, Antonio Galina, Marcelo A. Mori, Monica Montero-Lomeli, Claudio A. Masuda
    Journal of Biological Chemistry, 2020
    In the presence of galactose, lithium ions activate the unfolded protein response (UPR) by inhibiting phosphoglucomutase activity and causing the accumulation of galactose-related metabolites, including galactose-1-phosphate. These metabolites also accumulate in humans who have the disease classic galactosemia. Here, we demonstrate that Saccharomyces cerevisiae yeast strains harboring a deletion of UBX4, a gene encoding a partner of Cdc48p in the endoplasmic reticulum–associated degradation (ERAD) pathway, exhibit delayed UPR activation after lithium and galactose exposure because the deletion decreases galactose-1-phosphate levels. The delay in UPR activation did not occur in yeast strains in which key ERAD or proteasomal pathway genes had been disrupted, indicating that the ubx4Δ phenotype is ERAD-independent. We also observed that the ubx4Δ strain displays decreased oxygen consumption. The inhibition of mitochondrial respiration was sufficient to diminish galactose-1-phosphate levels and, consequently, affects UPR activation. Finally, we show that the deletion of the AMP-activated protein kinase ortholog–encoding gene SNF1 can restore the oxygen consumption rate in ubx4Δ strain, thereby reestablishing galactose metabolism, UPR activation, and cellular adaption to lithium–galactose challenge. Our results indicate a role for Ubx4p in yeast mitochondrial function and highlight that mitochondrial and endoplasmic reticulum functions are intertwined through galactose metabolism. These findings also shed new light on the mechanisms of lithium action and on the pathophysiology of galactosemia.
  • Induction of triacylglycerol synthesis in yeast by cell cycle arrest
    Juliana B Madeira, Gabriel S Matos, Laryssa S Messias, Bruno L Bozaquel-Morais, Claudio A Masuda, Monica Montero-Lomeli
    FEMS Yeast Research, 2019
    In this study, we found that cell cycle arrest induced by alpha-factor mating pheromone (G1), hydroxyurea (S) or nocodazole (G2/M) was associated to increased lipid droplet (LD) content. To identify novel cell cycle genes involved in LD homeostasis, we screened a deletion library for strains with altered LD levels. Among the mutants related to mitotic cell cycle, we found 24 hits that displayed a significantly higher LD content. Ontology mapping showed that neither a biological process nor a specific cell cycle phase was enriched among the hits. We decided to further study the role of SWI4 on LD homeostasis as it is involved in G1/S transition, a stage where lipolysis is active. The high LD content of swi4Δ mutant was not due to inhibition of lipolysis, but due to an increase in triacylglycerol (TAG) synthesis. In addition, deletion of the AMP kinase gene SNF1 or inhibition of TORC1 activity, both known regulators of LD homeostasis, further increased the LD content of a swi4Δ mutant. These findings highlight a role of the cell cycle regulator SWI4 in the coordination of lipid metabolism which is independent of the TORC1 and SNF1/AMPK pathways.
  • Protein phosphatase sit4 affects lipid droplet synthesis and soraphen a resistance independent of its role in regulating elongator dependent tRNA modification
    Bruno Bozaquel-Morais, Leonie Vogt, Valentina D’Angelo, Raffael Schaffrath, Roland Klassen, Mónica Montero-Lomelí
    Biomolecules, 2018
    The protein phosphatase Sit4 has been shown to be required for lipogenesis and resistance against the acetyl-CoA carboxylase inhibitor soraphen A. Since Sit4 is also required for biosynthesis of Elongator dependent tRNA modifications such as 5-methoxycarbonylmethyluridine (mcm5U), we investigated the relevance of tRNA modifications in lipogenesis and soraphen A response. While sit4 and Elongator (elp3) mutants copy defects in mcm5U formation and stress sensitivity, they do not share soraphen A sensitivity and low lipid droplet (LD) phenotypes. In contrast to sit4, we found elp3 mutants to display partial soraphen A resistance and a high LD phenotype. Screening a collection of tRNA modification mutants additionally identified the tRNA pseudo-uridine synthase gene DEG1 to be required for soraphen A sensitivity. Since deg1 and elp3 share high LD and soraphen A resistance phenotypes, these are likely caused by translational defects. In support of this notion, we observe overexpression of tRNAGlnUUG suppresses lipolysis defects of deg1 mutants. Hence, the sit4 mutation results in a composite defect including tRNA modification deficiency and loss of Snf1 kinase dephosphorylation, which induce opposite effects on LD regulation. Importantly, however, the Snf1 kinase regulatory defects of the phosphatase mutant dominate over effects on LD regulation imposed by loss of the tRNA modification alone.
  • Lipid index determination by liquid fluorescence recovery in the fungal pathogen Ustilago maydis
    Lucero Romero-Aguilar, Mónica Montero-Lomeli, Juan Pablo Pardo, Guadalupe Guerra- Sánchez
    Journal of Visualized Experiments, 2018
    The article shows how to implement the LD index assay, which is a sensitive microplate assay to determine the accumulation of triacylglycerols (TAGs) in lipid droplets (LDs). LD index is obtained without lipid extraction. It allows measuring the LDs content in high-throughput experiments under different conditions such as growth in rich or nitrogen depleted media. Albeit the method was described for the first time to study the lipid droplet metabolism in Saccharomyces cerevisiae, it was successfully applied to the basidiomycete Ustilago maydis. Interestingly, and because LDs are organelles phylogenetically conserved in eukaryotic cells, the method can be applied to a large variety of cells, from yeast to mammalian cells. The LD index is based on the liquid fluorescence recovery assay (LFR) of the BODIPY 493/503 under quenching conditions, by the addition of cells fixed with formaldehyde. Potassium iodine is used as a fluorescence quencher. The ratio between the fluorescence and the optical density slopes is named LD index. Slopes are calculated from the straight lines obtained when BODIPY fluorescence and optical density at 600 nm (OD600) are plotted against sample addition. Optimal data quality is reflected by correlation coefficients equal or above 0.9 (r ≥ 0.9). Multiple samples can be read simultaneously as it can be implemented in a microplate. Since BODIPY 493/503 is a lipophilic fluorescent dye that partitions into the lipid droplets, it can be used in many types of cells that accumulate LDs.
  • The galactose-induced decrease in phosphate levels leads to toxicity in yeast models of galactosemia
    Caio M. Machado, Evandro A. De-Souza, Ana Luiza F.V. De-Queiroz, Felipe S.A. Pimentel, Guilherme F.S. Silva, Fabio M. Gomes, Mónica Montero-Lomelí, Claudio A. Masuda
    Biochimica Et Biophysica Acta Molecular Basis of Disease, 2017
  • A chemogenomic screen reveals novel Snf1p/AMPK independent regulators of acetyl-CoA carboxylase
    Bruno L. Bozaquel-Morais, Juliana B. Madeira, Thiago M. Venâncio, Thiago Pacheco-Rosa, Claudio A. Masuda, Monica Montero-Lomeli
    Plos One, 2017
  • Lipid droplet levels vary heterogeneously in response to simulated gastrointestinal stresses in different probiotic Saccharomyces cerevisiae strains
    Daniel Zamith-Miranda, Mariana L. Palma, Gabriel S. Matos, Johnathon G. Schiebel, Clarissa M. Maya-Monteiro, Marcos Aronovich, Patricia T. Bozza, Fernando A. Bozza, Leonardo Nimrichter, Monica Montero-Lomeli, Ernesto T.A. Marques, Flaviano S. Martins, Bruno Douradinha
    Journal of Functional Foods, 2016
  • Probiotic Saccharomyces cerevisiae strains as biotherapeutic tools: is there room for improvement?
    Mariana L. Palma, Daniel Zamith-Miranda, Flaviano S. Martins, Fernando A. Bozza, Leonardo Nimrichter, Mônica Montero-Lomeli, Ernesto T. A. Marques, Bruno Douradinha
    Applied Microbiology and Biotechnology, 2015
  • TORC1 inhibition induces lipid droplet replenishment in yeast
    Juliana B. Madeira, Claudio A. Masuda, Clarissa M. Maya-Monteiro, Gabriel Soares Matos, Mónica Montero-Lomelí, Bruno L. Bozaquel-Morais
    Molecular and Cellular Biology, 2015
  • The unfolded protein response has a protective role in yeast models of classic galactosemia
    Evandro A. De-Souza, Felipe S. A. Pimentel, Caio M. Machado, Larissa S. Martins, Wagner S. da-Silva, Mónica Montero-Lomelí, Claudio A. Masuda
    Dmm Disease Models and Mechanisms, 2014
  • Pyruvate decarboxylase activity is regulated by the Ser/Thr protein phosphatase Sit4p in the yeast Saccharomyces cerevisiae
    Leandro José de Assis, Russolina Benedeta Zingali, Claudio Akio Masuda, Silas Pessini Rodrigues, Monica Montero-Lomelí
    FEMS Yeast Research, 2013
  • Expression of the glucose transporter HXT1 involves the Ser-Thr protein phosphatase Sit4 in Saccharomyces cerevisiae
    Andréa A. Souza, Michel N. Miranda, Suelene F. da Silva, Bruno Bozaquel-Morais, Claudio A. Masuda, Michel Ghislain, Mónica Montero-Lomelí
    FEMS Yeast Research, 2012
  • A new fluorescence-based method identifies protein phosphatases regulating lipid droplet metabolism
    Bruno L. Bozaquel-Morais, Juliana B. Madeira, Clarissa M. Maya-Monteiro, Claudio A. Masuda, Mónica Montero-Lomeli
    Plos One, 2010
  • Erratum to Gene expression analysis during dengue virus infection in HepG2 cells reveals virus control of innate immune response [Journal of Infection, 60, (2010), 65-75]
    Thaís M. Conceição, Tatiana El-Bacha, Camila S.A. Villas-Bôas, Gerardo Coello, Jorge Ramírez, Monica Montero-Lomeli, Andrea T. Da Poian
    Journal of Infection, 2010
  • Glycogen synthesis in brain and astrocytes is inhibited by chronic lithium treatment
    Andréa de Almeida Souza, Gisele S. Seixas da Silva, Bianca S. Velez, Ana Beatriz Menezes Santoro, Mónica Montero-Lomelí
    Neuroscience Letters, 2010
  • The serine/threonine protein phosphatase Sit4p activates multidrug resistance in Saccharomyces cerevisiae
    Michel N. Miranda, Claudio A. Masuda, Antonio Ferreira-Pereira, Elvira Carvajal, Michel Ghislain, Mónica Montero-Lomelí
    FEMS Yeast Research, 2010
  • Structural and functional study of Yer067w, a new protein involved in yeast metabolism control and drug resistance
    Tatiana Domitrovic, Guennadi Kozlov, João Claudio Gonçalves Freire, Claudio Akio Masuda, Marcius da Silva Almeida, Mónica Montero-Lomeli, Georgia Correa Atella, Edna Matta-Camacho, Kalle Gehring, Eleonora Kurtenbach
    Plos One, 2010
  • Gene expression analysis during dengue virus infection in HepG2 cells reveals virus control of innate immune response
    Thaís M. Conceição, Tatiana El-Bacha, Camila S.A. Villas-Bôas, Gerardo Coello, Jorge Ramírez, Monica Montero-Lomeli, Andrea T. Da Poian
    Journal of Infection, 2010
  • A fluorescent mutant of the NM domain of the yeast prion Sup35 provides insight into fibril formation and stability
    Fernando L. Palhano, Cristiane B. Rocha, Alexandre Bernardino, Gilberto Weissmuller, Claudio A. Masuda, Mônica Montero-Lomelí, André Marco Gomes, Peter Chien, Patrícia M. B. Fernandes, Debora Foguel
    Biochemistry, 2009
  • Dengue virus-induced regulation of the host cell translational machinery
    C.S.A. Villas-Bôas, T.M. Conceição, J. Ramírez, A.B.M. Santoro, A.T. Da Poian, M. Montero-Lomelí
    Brazilian Journal of Medical and Biological Research, 2009
  • Overexpression of the aldose reductase GRE3 suppresses lithium-induced galactose toxicity in Saccharomyces cerevisiae
    Claudio A. Masuda, Jose O. Previato, Michel N. Miranda, Leandro J. Assis, Luciana L. Penha, Lucia Mendonça-Previato, Mónica Montero-Lomelí
    FEMS Yeast Research, 2008
  • Lithium-mediated suppression of morphogenesis and growth in Candida albicans
    Layla F. Martins, Monica Montero-Lomelí, Claudio A. Masuda, Fabio S.A. Fortes, Jose O. Previato, Lucia Mendonça-Previato
    FEMS Yeast Research, 2008
  • Erythrocyte phosphoglucomutase activity of bipolar I patients currently using lithium or carbamazepine
    M. Montero-Lomelí, D. Galvão, B.B. Morais, A.E. Nardi
    Brazilian Journal of Medical and Biological Research, 2007
  • Deviation of carbohydrate metabolism by the SIT4 phosphatase in Saccharomyces cerevisiae
    Willy Jablonka, Simón Guzmán, Jorge Ramírez, Mónica Montero-Lomelí
    Biochimica Et Biophysica Acta General Subjects, 2006
  • Low resolution structure of the human α4 protein (IgBP1) and studies on the stability of α4 and of its yeast ortholog Tap42
    Juliana Helena Costa Smetana, Cristiano Luiz Pinto Oliveira, Willy Jablonka, Thelma Aguiar Pertinhez, Flavia Raquel Gonçalves Carneiro, Monica Montero-Lomeli, Iris Torriani, Nilson Ivo Tonin Zanchin
    Biochimica Et Biophysica Acta Proteins and Proteomics, 2006
  • Transcriptional, proteomic, and metabolic responses to lithium in galactose-grown yeast cells
    Christoffer Bro, Birgitte Regenberg, Gilles Lagniel, Jean Labarre, Mónica Montero-Lomelí, Jens Nielsen
    Journal of Biological Chemistry, 2003
  • The initiation factor eIF4A is involved in the response to lithium stress in Saccharomyces cerevisiae
    Mónica Montero-Lomelı́, Bruno L.B. Morais, Daniela L. Figueiredo, Domingos C.S. Neto, João R.P. Martins, Claudio A. Masuda
    Journal of Biological Chemistry, 2002
  • A DnaJ-like Protein Homologous to the Yeast Co-chaperone Sis1 (TcJ6p) Is Involved in Initiation of Translation in Trypanosoma cruzi
    Didier Salmon, Mónica Montero-Lomelı́, Samuel Goldenberg
    Journal of Biological Chemistry, 2001
  • Phosphoglucomutase is an in vivo lithium target in yeast
    Claudio A. Masuda, Marcelle A. Xavier, Katherine A. Mattos, Antonio Galina, Mónica Montero-Lomelı́
    Journal of Biological Chemistry, 2001
  • Regulation of monovalent ion homeostasis and pH by the Ser-Thr protein phosphatase SIT4 in Saccharomyces cerevisiae
    Claudio A. Masuda, Jorge Ramı́rez, Antonio Peña, Mónica Montero-Lomelı́
    Journal of Biological Chemistry, 2000
  • Structural study of the porcine Na+/H+ exchanger NHE1 gene and its 5'-flanking region
    Molecular and Cellular Biochemistry, 2000
  • An NH2-terminal deleted plasma membrane H+-ATPase is a dominant negative mutant and is sequestered in endoplasmic reticulum derived structures
    Claudio Akio Masuda, Mónica Montero-Lomelí
    Biochemistry and Cell Biology, 2000
  • Sarcoplasmic reticulum Ca2+ -ATPase of sea cucumber smooth muscle: Regulation by K+ and ATP
    Ana Maria Landeira-Fernandez, Antonio Galina, Paula Jennings, Monica Montero-Lomeli, Leopoldo de Meis
    Comparative Biochemistry and Physiology A Molecular and Integrative Physiology, 2000
  • Expression of a mammalian Na+/H+ antiporter in Saccharomyces cerevisiae
    Mónica Montero-Lomelí, Anna L. Okorokova Façanha.
    Biochemistry and Cell Biology, 1999
  • H+/K+ exchange in reconstituted yeast plasma membrane vesicles
    Jorge Ramírez, Antonio Peña, Mónica Montero-Lomelí
    Biochimica Et Biophysica Acta Biomembranes, 1996
  • Effect of dimethyl sulfoxide on phosphoryl transfer catalyzed by yeast hexokinase
    Mónica Montero-Lomelí
    Biochimica Et Biophysica Acta Bba Protein Structure and Molecular, 1992
  • Glucose 6-phosphate and hexokinase can be used as an ATP-regenerating system by the Ca2+-ATPase of sarcoplasmic reticulum
    Journal of Biological Chemistry, 1992
  • The Maxwell Demon in Biological Systems: Use of Glucose 6‐Phosphate and Hexokinase as an ATP Regenerating System by the Ca2+‐ATPase of Sarcoplasmic Reticulum and Submitochondrial Particles
    LEOPOLDO de MEIS, MONICA MONTERO‐LOMELÍ, MARIA ANGELA B. GRIECO, ANTONIO GALINA
    Annals of the New York Academy of Sciences, 1992
  • K+-and Mg2+-dependent hydrolysis of acetyl phosphate catalyzed by the (Ca2+ + Mg2+)-ATPase of sarcoplasmic reticulum
    Eduardo N. Chini, Monica Montero-Lomeli, Leopoldo de Meis
    Bba Biomembranes, 1990
  • Coupling of ATP hydrolysis to phosphate uptake in Rhodospirillum rubrum chromatophores under the influence of Ca2+ and Mg2+
    Journal of Biological Chemistry, 1989
  • Effect of ADP on the rate of acetyl phosphate hydrolysis by the Ca2+‐ATPase of sarcoplasmic reticulum
    Mónica MONTERO‐LOMELI, Leopoldo DE MEIS
    European Journal of Biochemistry, 1989
  • Activation of Mg-ATP hydrolysis in isolated Rhodospirillum rubrum H+-ATPase
    Mónica Montero-Lomelí, Georges Dreyfus
    Archives of Biochemistry and Biophysics, 1987