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Article ; Online: Separation of Volatile Organic Compounds in TAMOF-1.

González-Galán, Carmen / de Fez-Febré, Mabel / Giancola, Stefano / González-Cobos, Jesús / Vidal-Ferran, Anton / Galán-Mascarós, José Ramón / Balestra, Salvador R G / Calero, Sofía

ACS applied materials & interfaces

2022 Volume 14, Issue 27, Page(s) 30772–30785

Abstract: Separation of volatile organic compounds is one of the most studied processes in industry. TAMOF-1 is a homochiral metal-organic framework with a crystalline network of interconnected ≈1 nm channels and has high thermal and chemical stability. Thanks to ... ...

Abstract	Separation of volatile organic compounds is one of the most studied processes in industry. TAMOF-1 is a homochiral metal-organic framework with a crystalline network of interconnected ≈1 nm channels and has high thermal and chemical stability. Thanks to these features, it can resolve racemic mixtures of chiral drugs as a chiral stationary phase in chromatography. Interestingly, the particular shape and size of its channels, along with the presence of metallic centers and functional groups, allow establishing weak but significant interactions with guest molecules. This opens interesting possibilities not only to resolve racemates but also to separate other organic mixtures, such as saturated/unsaturated and/or linear/branched molecules. In search of these applications, we have studied the separation of volatile organic compounds in TAMOF-1. Monte Carlo simulations in the grand-canonical ensemble have been carried out to evaluate the separation of the selected molecules. Our results predict that TAMOF-1 is able to separate xylene isomers, hexane isomers, and benzene-cyclohexane mixtures. Experimental breakthrough analysis in the gas phase and also in the liquid phase confirms these predictions. Beds of TAMOF-1 are able to recognize the substitution in xylenes and the branching in hexanes, yielding excellent separation and reproducibility, thanks to the chemical and mechanical features of this material.
Language	English
Publishing date	2022-07-01
Publishing country	United States
Document type	Journal Article
ISSN	1944-8252
ISSN (online)	1944-8252
DOI	10.1021/acsami.2c05223
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Article ; Online: Author Correction: Sustainable oxygen evolution electrocatalysis in aqueous 1 M H

Yu, Jiahao / Garcés-Pineda, Felipe A / González-Cobos, Jesús / Peña-Díaz, Marina / Rogero, Celia / Giménez, Sixto / Spadaro, Maria Chiara / Arbiol, Jordi / Barja, Sara / Galán-Mascarós, José Ramón

Nature communications

2022 Volume 13, Issue 1, Page(s) 4687

Language	English
Publishing date	2022-08-10
Publishing country	England
Document type	Published Erratum
ZDB-ID	2553671-0
ISSN	2041-1723 ; 2041-1723
ISSN (online)	2041-1723
ISSN	2041-1723
DOI	10.1038/s41467-022-32399-6
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Article ; Online: Sustainable oxygen evolution electrocatalysis in aqueous 1 M H

Nature communications

2022 Volume 13, Issue 1, Page(s) 4341

Abstract: Earth-abundant electrocatalysts for the oxygen evolution reaction (OER) able to work in acidic working conditions are elusive. While many first-row transition metal oxides are competitive in alkaline media, most of them just dissolve or become inactive ... ...

Abstract	Earth-abundant electrocatalysts for the oxygen evolution reaction (OER) able to work in acidic working conditions are elusive. While many first-row transition metal oxides are competitive in alkaline media, most of them just dissolve or become inactive at high proton concentrations where hydrogen evolution is preferred. Only noble-metal catalysts, such as IrO
Language	English
Publishing date	2022-07-27
Publishing country	England
Document type	Journal Article
ZDB-ID	2553671-0
ISSN	2041-1723 ; 2041-1723
ISSN (online)	2041-1723
ISSN	2041-1723
DOI	10.1038/s41467-022-32024-6
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Article: Separation of Volatile Organic Compounds in TAMOF-1

González-Galán, Carmen / de Fez-Febré, Mabel / Giancola, Stefano / González-Cobos, Jesús / Vidal-Ferran, Anton / Galán-Mascarós, José Ramón / Balestra, Salvador R. G. / Calero, Sofía

ACS applied materials & interfaces. 2022 July 01, v. 14, no. 27

2022

Abstract: Separation of volatile organic compounds is one of the most studied processes in industry. TAMOF-1 is a homochiral metal–organic framework with a crystalline network of interconnected ≈1 nm channels and has high thermal and chemical stability. Thanks to ... ...

Abstract	Separation of volatile organic compounds is one of the most studied processes in industry. TAMOF-1 is a homochiral metal–organic framework with a crystalline network of interconnected ≈1 nm channels and has high thermal and chemical stability. Thanks to these features, it can resolve racemic mixtures of chiral drugs as a chiral stationary phase in chromatography. Interestingly, the particular shape and size of its channels, along with the presence of metallic centers and functional groups, allow establishing weak but significant interactions with guest molecules. This opens interesting possibilities not only to resolve racemates but also to separate other organic mixtures, such as saturated/unsaturated and/or linear/branched molecules. In search of these applications, we have studied the separation of volatile organic compounds in TAMOF-1. Monte Carlo simulations in the grand-canonical ensemble have been carried out to evaluate the separation of the selected molecules. Our results predict that TAMOF-1 is able to separate xylene isomers, hexane isomers, and benzene–cyclohexane mixtures. Experimental breakthrough analysis in the gas phase and also in the liquid phase confirms these predictions. Beds of TAMOF-1 are able to recognize the substitution in xylenes and the branching in hexanes, yielding excellent separation and reproducibility, thanks to the chemical and mechanical features of this material.
Keywords	chromatography ; coordination polymers ; hexane ; industry ; liquids ; volatile organic compounds ; xylene
Language	English
Dates of publication	2022-0701
Size	p. 30772-30785.
Publishing place	American Chemical Society
Document type	Article
ISSN	1944-8252
DOI	10.1021/acsami.2c05223
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Article ; Online: Leukotriene-C4 synthase, a critical enzyme in the activation of store-independent Orai1/Orai3 channels, is required for neointimal hyperplasia.

Zhang, Wei / Zhang, Xuexin / González-Cobos, José C / Stolwijk, Judith A / Matrougui, Khalid / Trebak, Mohamed

The Journal of biological chemistry

2014 Volume 290, Issue 8, Page(s) 5015–5027

Abstract: Leukotriene-C4 synthase (LTC4S) generates LTC4 from arachidonic acid metabolism. LTC4 is a proinflammatory factor that acts on plasma membrane cysteinyl leukotriene receptors. Recently, however, we showed that LTC4 was also a cytosolic second messenger ... ...

Abstract	Leukotriene-C4 synthase (LTC4S) generates LTC4 from arachidonic acid metabolism. LTC4 is a proinflammatory factor that acts on plasma membrane cysteinyl leukotriene receptors. Recently, however, we showed that LTC4 was also a cytosolic second messenger that activated store-independent LTC4-regulated Ca(2+) (LRC) channels encoded by Orai1/Orai3 heteromultimers in vascular smooth muscle cells (VSMCs). We showed that Orai3 and LRC currents were up-regulated in medial and neointimal VSMCs after vascular injury and that Orai3 knockdown inhibited LRC currents and neointimal hyperplasia. However, the role of LTC4S in neointima formation remains unknown. Here we show that LTC4S knockdown inhibited LRC currents in VSMCs. We performed in vivo experiments where rat left carotid arteries were injured using balloon angioplasty to cause neointimal hyperplasia. Neointima formation was associated with up-regulation of LTC4S protein expression in VSMCs. Inhibition of LTC4S expression in injured carotids by lentiviral particles encoding shRNA inhibited neointima formation and inward and outward vessel remodeling. LRC current activation did not cause nuclear factor for activated T cells (NFAT) nuclear translocation in VSMCs. Surprisingly, knockdown of either LTC4S or Orai3 yielded more robust and sustained Akt1 and Akt2 phosphorylation on Ser-473/Ser-474 upon serum stimulation. LTC4S and Orai3 knockdown inhibited VSMC migration in vitro with no effect on proliferation. Akt activity was suppressed in neointimal and medial VSMCs from injured vessels at 2 weeks postinjury but was restored when the up-regulation of either LTC4S or Orai3 was prevented by shRNA. We conclude that LTC4S and Orai3 altered Akt signaling to promote VSMC migration and neointima formation.
MeSH term(s)	Animals ; Calcium Channels/genetics ; Calcium Channels/metabolism ; Gene Expression Regulation, Enzymologic/genetics ; Glutathione Transferase/biosynthesis ; Glutathione Transferase/genetics ; Hyperplasia/genetics ; Hyperplasia/metabolism ; Hyperplasia/pathology ; Male ; Muscle, Smooth, Vascular/metabolism ; Muscle, Smooth, Vascular/pathology ; Myocytes, Smooth Muscle/metabolism ; Myocytes, Smooth Muscle/pathology ; NFATC Transcription Factors/genetics ; NFATC Transcription Factors/metabolism ; Neointima/genetics ; Neointima/metabolism ; Neointima/pathology ; ORAI1 Protein ; Phosphorylation/genetics ; Proto-Oncogene Proteins c-akt/genetics ; Proto-Oncogene Proteins c-akt/metabolism ; Rats ; Rats, Sprague-Dawley ; Signal Transduction/genetics
Chemical Substances	Calcium Channels ; NFATC Transcription Factors ; ORAI1 Protein ; Orai1 protein, rat ; Orai3 protein, rat ; Glutathione Transferase (EC 2.5.1.18) ; Akt1 protein, rat (EC 2.7.11.1) ; Akt2 protein, rat (EC 2.7.11.1) ; Proto-Oncogene Proteins c-akt (EC 2.7.11.1) ; leukotriene-C4 synthase (EC 4.4.1.20)
Language	English
Publishing date	2014-12-24
Publishing country	United States
Document type	Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
ZDB-ID	2997-x
ISSN	1083-351X ; 0021-9258
ISSN (online)	1083-351X
ISSN	0021-9258
DOI	10.1074/jbc.M114.625822
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Article ; Online: Smooth muscle CaMKIIδ promotes allergen-induced airway hyperresponsiveness and inflammation.

Spinelli, Amy M / Liu, Yongfeng / Sun, Li-Yan / González-Cobos, José C / Backs, Johannes / Trebak, Mohamed / Singer, Harold A

Pflugers Archiv : European journal of physiology

2015 Volume 467, Issue 12, Page(s) 2541–2554

Abstract: Airway smooth muscle (ASM) is a key target cell in allergen-induced asthma known to contribute to airway hyperresponsiveness (AHR) and chronic airway remodeling. Changes in ASM calcium homeostasis have been shown to contribute to AHR although the ... ...

Abstract	Airway smooth muscle (ASM) is a key target cell in allergen-induced asthma known to contribute to airway hyperresponsiveness (AHR) and chronic airway remodeling. Changes in ASM calcium homeostasis have been shown to contribute to AHR although the mechanisms and Ca(2+) signal effectors are incompletely understood. In the present study, we tested the function of ASM multifunctional protein kinase Ca(2+)/calmodulin-dependent kinase II (CaMKII) isoforms CaMKIIδ and CaMKIIγ in allergen-induced AHR and airway remodeling in vivo. Using a murine model of atopic asthma, we demonstrate that CaMKIIδ protein is upregulated in ASM derived from ovalbumin (OVA)-treated animals compared to controls. A genetic approach to conditionally knock out smooth muscle CaMKIIδ and CaMKIIγ in separate Cre-loxp systems was validated, and using this loss-of-function approach, the function of these CaMKII isoforms was tested in ovalbumin (OVA)-induced airway remodeling and AHR. OVA treatment in control mice had no effect on ASM remodeling in this model of AHR, and CaMKIIδ knockouts had no independent effects on ASM content. However, at 1 day post-final OVA challenge, OVA-induced AHR was eliminated in the CaMKIIδ knockouts. OVA-induced peribronchial inflammation and bronchoalveolar lavage fluid (BALF) levels of the Th2 cytokine IL-13 were significantly decreased in the CaMKIIδ knockouts. Unexpectedly, we found increased peribronchial eosinophils in the smooth muscle CaMKIIδ knockouts compared to control animals at 1 day post-final challenge, suggesting that lack of ASM CaMKIIδ delays the progression of AHR rather than inhibiting it. Indeed, when AHR was determined at 7 days post-final OVA challenge, CaMKIIδ knockouts showed robust AHR while AHR was fully resolved in OVA-challenged control mice. These in vivo studies demonstrate a role for smooth muscle CaMKIIδ in promoting airway inflammation and AHR and suggest a complex signaling role for CaMKIIδ in regulating ASM function. These studies confirm the diverse roles of ASM cells as immune effectors that control AHR and call for further studies into CaMKIIδ-mediated signaling in ASM cells during disease.
MeSH term(s)	Airway Remodeling ; Animals ; Asthma/metabolism ; Asthma/pathology ; Calcium-Calmodulin-Dependent Protein Kinase Type 2/genetics ; Calcium-Calmodulin-Dependent Protein Kinase Type 2/metabolism ; Inflammation/metabolism ; Interleukin-13/genetics ; Interleukin-13/metabolism ; Isoenzymes/genetics ; Isoenzymes/metabolism ; Male ; Mice ; Muscle, Smooth/drug effects ; Muscle, Smooth/metabolism ; Ovalbumin/toxicity
Chemical Substances	Interleukin-13 ; Isoenzymes ; Ovalbumin (9006-59-1) ; Calcium-Calmodulin-Dependent Protein Kinase Type 2 (EC 2.7.11.17)
Language	English
Publishing date	2015-12
Publishing country	Germany
Document type	Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
ZDB-ID	6380-0
ISSN	1432-2013 ; 0031-6768
ISSN (online)	1432-2013
ISSN	0031-6768
DOI	10.1007/s00424-015-1713-5
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Article ; Online: Complex role of STIM1 in the activation of store-independent Orai1/3 channels.

Zhang, Xuexin / Zhang, Wei / González-Cobos, José C / Jardin, Isaac / Romanin, Christoph / Matrougui, Khalid / Trebak, Mohamed

The Journal of general physiology

2014 Volume 143, Issue 3, Page(s) 345–359

Abstract: Orai proteins contribute to Ca(2+) entry into cells through both store-dependent, Ca(2+) release-activated Ca(2+) (CRAC) channels (Orai1) and store-independent, arachidonic acid (AA)-regulated Ca(2+) (ARC) and leukotriene C4 (LTC4)-regulated Ca(2+) (LRC) ...

Abstract	Orai proteins contribute to Ca(2+) entry into cells through both store-dependent, Ca(2+) release-activated Ca(2+) (CRAC) channels (Orai1) and store-independent, arachidonic acid (AA)-regulated Ca(2+) (ARC) and leukotriene C4 (LTC4)-regulated Ca(2+) (LRC) channels (Orai1/3 heteromultimers). Although activated by fundamentally different mechanisms, CRAC channels, like ARC and LRC channels, require stromal interacting molecule 1 (STIM1). The role of endoplasmic reticulum-resident STIM1 (ER-STIM1) in CRAC channel activation is widely accepted. Although ER-STIM1 is necessary and sufficient for LRC channel activation in vascular smooth muscle cells (VSMCs), the minor pool of STIM1 located at the plasma membrane (PM-STIM1) is necessary for ARC channel activation in HEK293 cells. To determine whether ARC and LRC conductances are mediated by the same or different populations of STIM1, Orai1, and Orai3 proteins, we used whole-cell and perforated patch-clamp recording to compare AA- and LTC4-activated currents in VSMCs and HEK293 cells. We found that both cell types show indistinguishable nonadditive LTC4- and AA-activated currents that require both Orai1 and Orai3, suggesting that both conductances are mediated by the same channel. Experiments using a nonmetabolizable form of AA or an inhibitor of 5-lipooxygenase suggested that ARC and LRC currents in both cell types could be activated by either LTC4 or AA, with LTC4 being more potent. Although PM-STIM1 was required for current activation by LTC4 and AA under whole-cell patch-clamp recordings in both cell types, ER-STIM1 was sufficient with perforated patch recordings. These results demonstrate that ARC and LRC currents are mediated by the same cellular populations of STIM1, Orai1, and Orai3, and suggest a complex role for both ER-STIM1 and PM-STIM1 in regulating these store-independent Orai1/3 channels.
MeSH term(s)	Action Potentials ; Animals ; Arachidonic Acid/pharmacology ; Calcium/metabolism ; Calcium Channels/metabolism ; Calcium Signaling ; Cell Membrane/metabolism ; Cells, Cultured ; Endoplasmic Reticulum/metabolism ; HEK293 Cells ; Humans ; Leukotriene C4/pharmacology ; Membrane Glycoproteins/metabolism ; Muscle, Smooth, Vascular/cytology ; Muscle, Smooth, Vascular/metabolism ; Myocytes, Smooth Muscle/drug effects ; Myocytes, Smooth Muscle/metabolism ; Myocytes, Smooth Muscle/physiology ; ORAI1 Protein ; Rats ; Stromal Interaction Molecule 1
Chemical Substances	Calcium Channels ; Membrane Glycoproteins ; ORAI1 Protein ; Orai1 protein, rat ; Orai3 protein, rat ; Stim1 protein, rat ; Stromal Interaction Molecule 1 ; Arachidonic Acid (27YG812J1I) ; Leukotriene C4 (2CU6TT9V48) ; Calcium (SY7Q814VUP)
Language	English
Publishing date	2014-02-24
Publishing country	United States
Document type	Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
ZDB-ID	3118-5
ISSN	1540-7748 ; 0022-1295
ISSN (online)	1540-7748
ISSN	0022-1295
DOI	10.1085/jgp.201311084
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Article ; Online: TRPC channels in smooth muscle cells.

Gonzalez-Cobos, Jose C / Trebak, Mohamed

Frontiers in bioscience (Landmark edition)

2010 Volume 15, Issue 3, Page(s) 1023–1039

Abstract: Transient receptor potential canonical (TRPC) proteins constitute a family of seven (TRPC1-7) nonselective cation channels within the wider TRP superfamily. TRPC1, TRPC3, TRPC4, TRPC5 and TRPC6 channels are expressed in vascular smooth muscle cells from ... ...

Abstract	Transient receptor potential canonical (TRPC) proteins constitute a family of seven (TRPC1-7) nonselective cation channels within the wider TRP superfamily. TRPC1, TRPC3, TRPC4, TRPC5 and TRPC6 channels are expressed in vascular smooth muscle cells from human vessels of all calibers and in smooth muscle from organs such as the uterus and the gastrointestinal tract. TRPC channels have recently emerged as important players in the control of smooth muscle function. This review will focus on the retrospective analysis of studies proposing contributions of TRPC channels to native calcium entry pathways in smooth muscle and to physiological and pathophysiological responses with emphasis on the vascular system.
MeSH term(s)	Calcium/metabolism ; Female ; Gastrointestinal Tract/metabolism ; Humans ; Muscle, Smooth, Vascular/cytology ; Muscle, Smooth, Vascular/metabolism ; Protein Isoforms/metabolism ; Signal Transduction ; TRPC Cation Channels/metabolism ; Uterus/metabolism ; Vascular Diseases/metabolism ; Vascular Diseases/pathology
Chemical Substances	Protein Isoforms ; TRPC Cation Channels ; transient receptor potential cation channel, subfamily C, member 1 ; Calcium (SY7Q814VUP)
Language	English
Publishing date	2010-06-01
Publishing country	Singapore
Document type	Journal Article ; Research Support, N.I.H., Extramural ; Review
ZDB-ID	2704569-9
ISSN	2768-6698 ; 1093-9946
ISSN (online)	2768-6698
ISSN	1093-9946
DOI	10.2741/3660
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Article ; Online: Homochiral Metal-Organic Frameworks for Enantioselective Separations in Liquid Chromatography.

Corella-Ochoa, M Nieves / Tapia, Jesús B / Rubin, Heather N / Lillo, Vanesa / González-Cobos, Jesús / Núñez-Rico, José Luis / Balestra, Salvador R G / Almora-Barrios, Neyvis / Lledós, Marina / Güell-Bara, Arnau / Cabezas-Giménez, Juanjo / Escudero-Adán, Eduardo C / Vidal-Ferran, Anton / Calero, Sofía / Reynolds, Melissa / Martí-Gastaldo, Carlos / Galán-Mascarós, José Ramón

Journal of the American Chemical Society

2019 Volume 141, Issue 36, Page(s) 14306–14316

Abstract: Selective separation of enantiomers is a substantial challenge for the pharmaceutical industry. Chromatography on chiral stationary phases is the standard method, but at a very high cost for industrial-scale purification due to the high cost of the ... ...

Abstract	Selective separation of enantiomers is a substantial challenge for the pharmaceutical industry. Chromatography on chiral stationary phases is the standard method, but at a very high cost for industrial-scale purification due to the high cost of the chiral stationary phases. Typically, these materials are poorly robust, expensive to manufacture, and often too specific for a single desired substrate, lacking desirable versatility across different chiral analytes. Here, we disclose a porous, robust homochiral metal-organic framework (MOF),
MeSH term(s)	Chromatography, High Pressure Liquid ; Copper/chemistry ; Metal-Organic Frameworks/chemistry ; Metal-Organic Frameworks/isolation & purification ; Molecular Structure ; Stereoisomerism ; Water/chemistry
Chemical Substances	Metal-Organic Frameworks ; Water (059QF0KO0R) ; Copper (789U1901C5)
Language	English
Publishing date	2019-09-03
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
ZDB-ID	3155-0
ISSN	1520-5126 ; 0002-7863
ISSN (online)	1520-5126
ISSN	0002-7863
DOI	10.1021/jacs.9b06500
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Article: Changes in the Microbial Composition of the Rhizosphere of Hop Plants Affected by Verticillium Wilt Caused by

Gallego-Clemente, Elena / Moreno-González, Víctor / Ibáñez, Ana / Calvo-Peña, Carla / Ghoreshizadeh, Seyedehtannaz / Radišek, Sebastjan / Cobos, Rebeca / Coque, Juan José R

Microorganisms

2023 Volume 11, Issue 7

Abstract: Verticillium wilt is a devastating disease affecting many crops, including hops. This study aims to describe fungal and bacterial populations associated with bulk and rhizosphere soils in a hop field cultivated in Slovenia with the Celeia variety, which ... ...

Abstract	Verticillium wilt is a devastating disease affecting many crops, including hops. This study aims to describe fungal and bacterial populations associated with bulk and rhizosphere soils in a hop field cultivated in Slovenia with the Celeia variety, which is highly susceptible to
Language	English
Publishing date	2023-07-16
Publishing country	Switzerland
Document type	Journal Article
ZDB-ID	2720891-6
ISSN	2076-2607
ISSN	2076-2607
DOI	10.3390/microorganisms11071819
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