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Article ; Online: C

Kong, Lingyu / Chou, Yajie / Albalat, Muriel / Jean, Marion / Vanthuyne, Nicolas / Humbel, Stéphane / Nava, Paola / Clavier, Hervé

Dalton transactions (Cambridge, England : 2003)

2023 Volume 52, Issue 25, Page(s) 8728–8736

Abstract: The concept of atropisomeric N-heterocyclic carbene (NHC)-metal complexes was extended to NHCs possessing ... ...

Abstract	The concept of atropisomeric N-heterocyclic carbene (NHC)-metal complexes was extended to NHCs possessing a
Language	English
Publishing date	2023-06-27
Publishing country	England
Document type	Journal Article
ZDB-ID	1472887-4
ISSN	1477-9234 ; 1364-5447 ; 0300-9246 ; 1477-9226
ISSN (online)	1477-9234 ; 1364-5447
ISSN	0300-9246 ; 1477-9226
DOI	10.1039/d3dt01182h
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Article ; Online: Shifting the landscape: Dominant C-terminal rare missense FOXL2 variants in non-syndromic primary ovarian failure etiology.

Clinical genetics

2024

Abstract: ... in the C-terminal region of FOXL2 are high-risk factors for non-syndromic POI/DOR, though FOXL2 gene ...

Abstract	Pathogenic germline variants in the FOXL2 gene are associated with Blepharophimosis, Ptosis, and Epicanthus Inversus syndrome (BPES) in humans, an autosomal dominant condition. Two forms of BPES have emerged: (i) type I (BPES-I), characterized by ocular signs and primary ovarian failure (POI), and (ii) type II (BPES-II) with no systemic associations. This study aimed to compare the distribution of FOXL2 variants in idiopathic POI/DOR (diminished ovarian reserve) and both types of BPES, and to determine the involvement of FOXL2 in non-syndromic forms of POI/DOR. We studied the whole coding region of the FOXL2 gene using next-generation sequencing in 1282 patients with non-syndromic POI/DOR. Each identified FOXL2 variant was compared to its frequency in the general population, considering ethnicity. Screening of the entire coding region of the FOXL2 gene allowed us to identify 10 different variants, including nine missense variants. Of the patients with POI/DOR, 14 (1%) carried a FOXL2 variant. Significantly, six out of nine missense variants (67%) were overrepresented in our POI/DOR cohort compared to the general or specific ethnic subgroups. Our findings strongly suggest that five rare missense variants, mainly located in the C-terminal region of FOXL2 are high-risk factors for non-syndromic POI/DOR, though FOXL2 gene implication accounts for approximately 0.54% of non-syndromic POI/DOR cases. These results support the implementation of routine genetic screening for patients with POI/DOR in clinical settings.
Language	English
Publishing date	2024-04-01
Publishing country	Denmark
Document type	Journal Article
ZDB-ID	221209-2
ISSN	1399-0004 ; 0009-9163
ISSN (online)	1399-0004
ISSN	0009-9163
DOI	10.1111/cge.14526
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Article ; Online: An adaptable platform for in-house hepatitis C serology.

Pedersen, Jannie / Moukandja, Irène Pegha / Ndidi, Stella / Sørensen, Anna-Louise / Koumakpayi, Ismaël Hervé / Lekana-Douki, Jean-Bernard / Vachon, Marie-Louise / Weis, Nina / Kobinger, Gary / Fausther-Bovendo, Hugues

Journal of virological methods

2022 Volume 308, Page(s) 114586

Abstract: ... an adaptable enzyme-linked immunoassay (ELISA) using hepatitis C virus (HCV) as a proof-of-concept application ...

Abstract	Serology-based diagnosis remains one of the major tools for diagnosis and surveillance of infectious diseases. However, for many neglected diseases no or only few commercial assays are available and often with prices prohibiting large scale testing in low and middle-income countries (LMICs). We developed an adaptable enzyme-linked immunoassay (ELISA) using hepatitis C virus (HCV) as a proof-of-concept application. By combining the maltose-binding-protein with a multiepitope HCV protein, we were able to obtain a high concentration of protein suitable for downstream applications. Following optimization, the assay was verified using previously tested human samples from Canada, Denmark and Gabon in parallel with the use of a commercial protein. Sensitivity and specificity were calculated to 98 % and 97 % respectively, after accounting for non-specific binding and assay optimization. This study provides a thorough description of the development, and validation of a multiepitope ELISA-based diagnostic assay against HCV, which could be implemented at low cost. The described methodology can be readily adapted to develop novel ELISA-based diagnostic assays for other infectious pathogens with well-described immunogenic epitopes. This method could improve the diagnosis of neglected diseases for which affordable diagnostic assays are lacking.
MeSH term(s)	Enzyme-Linked Immunosorbent Assay/methods ; Hepacivirus ; Hepatitis C/diagnosis ; Hepatitis C Antibodies ; Hepatitis C Antigens ; Humans ; Neglected Diseases ; Sensitivity and Specificity
Chemical Substances	Hepatitis C Antibodies ; Hepatitis C Antigens
Language	English
Publishing date	2022-07-16
Publishing country	Netherlands
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	8013-5
ISSN	1879-0984 ; 0166-0934
ISSN (online)	1879-0984
ISSN	0166-0934
DOI	10.1016/j.jviromet.2022.114586
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Article ; Online: Characterization of the physicochemical interactions between exenatide and two intestinal permeation enhancers: Sodium caprate (C

Twarog, Caroline / Fattal, Elias / Noiray, Magali / Illel, Brigitte / Brayden, David J / Taverna, Myriam / Hillaireau, Hervé

International journal of pharmaceutics

2022 Volume 626, Page(s) 122131

Abstract: ... caprate (C ...

Abstract	A common approach to tackle the poor intestinal membrane permeability of peptides after oral administration is to formulate them with a permeation enhancer (PE). Increased oral bioavailability for oral peptide candidates has been reported from clinical trials when either salcaprozate sodium (SNAC) or sodium caprate (C
MeSH term(s)	Bile Acids and Salts ; Caprylates ; Decanoic Acids ; Exenatide ; Glucagon-Like Peptide 1 ; Intestinal Absorption ; Micelles ; Peptides ; Water
Chemical Substances	Bile Acids and Salts ; Caprylates ; Decanoic Acids ; Micelles ; N-(8-(2-hydroxybenzoyl)amino)caprylate ; Peptides ; Water (059QF0KO0R) ; decanoic acid (4G9EDB6V73) ; Glucagon-Like Peptide 1 (89750-14-1) ; Exenatide (9P1872D4OL)
Language	English
Publishing date	2022-08-24
Publishing country	Netherlands
Document type	Journal Article
ZDB-ID	428962-6
ISSN	1873-3476 ; 0378-5173
ISSN (online)	1873-3476
ISSN	0378-5173
DOI	10.1016/j.ijpharm.2022.122131
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Article ; Online: C/EBPα Confers Dependence to Fatty Acid Anabolic Pathways and Vulnerability to Lipid Oxidative Stress-Induced Ferroptosis in FLT3-Mutant Leukemia.

Sabatier, Marie / Birsen, Rudy / Lauture, Laura / Mouche, Sarah / Angelino, Paolo / Dehairs, Jonas / Goupille, Léa / Boussaid, Ismael / Heiblig, Maël / Boet, Emeline / Sahal, Ambrine / Saland, Estelle / Santos, Juliana C / Armengol, Marc / Fernández-Serrano, Miranda / Farge, Thomas / Cognet, Guillaume / Simonetta, Federico / Pignon, Corentin /

Graffeuil, Antoine / Mazzotti, Céline / Avet-Loiseau, Hervé / Delos, Océane / Bertrand-Michel, Justine / Chedru, Amélie / Dembitz, Vilma / Gallipoli, Paolo / Anstee, Natasha S / Loo, Sun / Wei, Andrew H / Carroll, Martin / Goubard, Armelle / Castellano, Rémy / Collette, Yves / Vergez, François / Mansat-De Mas, Véronique / Bertoli, Sarah / Tavitian, Suzanne / Picard, Muriel / Récher, Christian / Bourges-Abella, Nathalie / Granat, Fanny / Kosmider, Olivier / Sujobert, Pierre / Colsch, Benoit / Joffre, Carine / Stuani, Lucille / Swinnen, Johannes V / Guillou, Hervé / Roué, Gael / Hakim, Nawad / Dejean, Anne S / Tsantoulis, Petros / Larrue, Clément / Bouscary, Didier / Tamburini, Jerome / Sarry, Jean-Emmanuel

Cancer discovery

2023 Volume 13, Issue 7, Page(s) 1720–1747

Abstract: Although transcription factor CCAAT-enhancer binding protein α (C/EBPα) is critical for normal and ... multiomics analyses uncovered a coordinated activation of C/EBPα and Fms-like tyrosine kinase 3 (FLT3 ... Mechanistically, C/EBPα regulated the fatty acid synthase (FASN)-stearoyl-CoA desaturase (SCD) axis to promote ...

Abstract	Although transcription factor CCAAT-enhancer binding protein α (C/EBPα) is critical for normal and leukemic differentiation, its role in cell and metabolic homeostasis is largely unknown in cancer. Here, multiomics analyses uncovered a coordinated activation of C/EBPα and Fms-like tyrosine kinase 3 (FLT3) that increased lipid anabolism in vivo and in patients with FLT3-mutant acute myeloid leukemia (AML). Mechanistically, C/EBPα regulated the fatty acid synthase (FASN)-stearoyl-CoA desaturase (SCD) axis to promote fatty acid (FA) biosynthesis and desaturation. We further demonstrated that FLT3 or C/EBPα inactivation decreased monounsaturated FA incorporation to membrane phospholipids through SCD downregulation. Consequently, SCD inhibition enhanced susceptibility to lipid redox stress that was exploited by combining FLT3 and glutathione peroxidase 4 inhibition to trigger lipid oxidative stress, enhancing ferroptotic death of FLT3-mutant AML cells. Altogether, our study reveals a C/EBPα function in lipid homeostasis and adaptation to redox stress, and a previously unreported vulnerability of FLT3-mutant AML to ferroptosis with promising therapeutic application. Significance: FLT3 mutations are found in 30% of AML cases and are actionable by tyrosine kinase inhibitors. Here, we discovered that C/EBPα regulates FA biosynthesis and protection from lipid redox stress downstream mutant-FLT3 signaling, which confers a vulnerability to ferroptosis upon FLT3 inhibition with therapeutic potential in AML. This article is highlighted in the In This Issue feature, p. 1501.
MeSH term(s)	Humans ; CCAAT-Enhancer-Binding Protein-alpha/genetics ; CCAAT-Enhancer-Binding Protein-alpha/metabolism ; fms-Like Tyrosine Kinase 3/genetics ; fms-Like Tyrosine Kinase 3/metabolism ; Ferroptosis ; Fatty Acids ; Leukemia, Myeloid, Acute/drug therapy ; Leukemia, Myeloid, Acute/genetics ; Leukemia, Myeloid, Acute/metabolism ; Mutation ; Oxidative Stress ; Protein Kinase Inhibitors/therapeutic use ; Cell Line, Tumor
Chemical Substances	CCAAT-Enhancer-Binding Protein-alpha ; fms-Like Tyrosine Kinase 3 (EC 2.7.10.1) ; Fatty Acids ; Protein Kinase Inhibitors ; FLT3 protein, human (EC 2.7.10.1)
Language	English
Publishing date	2023-04-03
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	2625242-9
ISSN	2159-8290 ; 2159-8274
ISSN (online)	2159-8290
ISSN	2159-8274
DOI	10.1158/2159-8290.CD-22-0411
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Article ; Online: Molecular interactions of PCSK9 with an inhibitory nanobody, CAP1 and HLA-C: Functional regulation of LDLR levels.

Fruchart Gaillard, Carole / Ouadda, Ali Ben Djoudi / Ciccone, Lidia / Girard, Emmanuelle / Mikaeeli, Sepideh / Evagelidis, Alexandra / Le Dévéhat, Maïlys / Susan-Resiga, Delia / Lajeunesse, Evelyne Cassar / Nozach, Hervé / Ramos, Oscar Henrique Pereira / Thureau, Aurélien / Legrand, Pierre / Prat, Annik / Dive, Vincent / Seidah, Nabil G

Molecular metabolism

2022 Volume 67, Page(s) 101662

Abstract: ... We previously suggested that out of the three M1, M2 and M3 subdomains of the C-terminal Cys/His-rich-domain ... on the LDLR. By modeling the previously reported interaction between M2 and an R-X-E motif in HLA-C ... PCSK9-CAP1 complex to these compartments after endocytosis into clathrin-coated vesicles, is HLA-C or ...

Abstract	Objective: The liver-derived circulating PCSK9 enhances the degradation of the LDL receptor (LDLR) in endosomes/lysosomes. PCSK9 inhibition or silencing is presently used in clinics worldwide to reduce LDL-cholesterol, resulting in lower incidence of cardiovascular disease and possibly cancer/metastasis. The mechanism by which the PCSK9-LDLR complex is sorted to degradation compartments is not fully understood. We previously suggested that out of the three M1, M2 and M3 subdomains of the C-terminal Cys/His-rich-domain (CHRD) of PCSK9, only M2 is critical for the activity of extracellular of PCSK9 on cell surface LDLR. This likely implicates the binding of M2 to an unknown membrane-associated "protein X" that would escort the complex to endosomes/lysosomes for degradation. We reported that a nanobody P1.40 binds the M1 and M3 domains of the CHRD and inhibits the function of PCSK9. It was also reported that the cytosolic adenylyl cyclase-associated protein 1 (CAP1) could bind M1 and M3 subdomains and enhance the activity of PCSK9. In this study, we determined the 3-dimensional structure of the CHRD-P1.40 complex to understand the intricate interplay between P1.40, CAP1 and PCSK9 and how they regulate LDLR degradation. Methods: X-ray diffraction of the CHRD-P1.40 complex was analyzed with a 2.2 Å resolution. The affinity and interaction of PCSK9 or CHRD with P1.40 or CAP1 was analyzed by atomic modeling, site-directed mutagenesis, bio-layer interferometry, expression in hepatic cell lines and immunocytochemistry to monitor LDLR degradation. The CHRD-P1.40 interaction was further analyzed by deep mutational scanning and binding assays to validate the role of predicted critical residues. Conformational changes and atomic models were obtained by small angle X-ray scattering (SAXS). Results: We demonstrate that PCSK9 exists in a closed or open conformation and that P1.40 favors the latter by binding key residues in the M1 and M3 subdomains of the CHRD. Our data show that CAP1 is well secreted by hepatic cells and binds extracellular PCSK9 at distinct residues in the M1 and M3 modules and in the acidic prodomain. CAP1 stabilizes the closed conformation of PCSK9 and prevents P1.40 binding. However, CAP1 siRNA only partially inhibited PCSK9 activity on the LDLR. By modeling the previously reported interaction between M2 and an R-X-E motif in HLA-C, we identified Glu Conclusions: The present study reveals that CAP1 enhances the function of PCSK9, likely by twisting the protein into a closed configuration that exposes the M2 subdomain needed for targeting the PCSK9-LDLR complex to degradation compartments. We hypothesize that "protein X", which is expected to guide the LDLR-PCSK9-CAP1 complex to these compartments after endocytosis into clathrin-coated vesicles, is HLA-C or a similar MHC-I family member. This conclusion is supported by the PCSK9 natural loss-of-function Q554E and gain-of-function H553R M2 variants, whose consequences are anticipated by our modeling.
MeSH term(s)	Proprotein Convertase 9/genetics ; Proprotein Convertase 9/metabolism ; HLA-C Antigens ; Serine Endopeptidases/metabolism ; Proprotein Convertases/genetics ; Proprotein Convertases/metabolism ; Scattering, Small Angle ; X-Ray Diffraction ; Receptors, LDL/metabolism
Chemical Substances	PCSK9 protein, human (EC 3.4.21.-) ; Proprotein Convertase 9 (EC 3.4.21.-) ; HLA-C Antigens ; Serine Endopeptidases (EC 3.4.21.-) ; Proprotein Convertases (EC 3.4.21.-) ; CAP1-6D ; Receptors, LDL
Language	English
Publishing date	2022-12-22
Publishing country	Germany
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	2708735-9
ISSN	2212-8778 ; 2212-8778
ISSN (online)	2212-8778
ISSN	2212-8778
DOI	10.1016/j.molmet.2022.101662
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Article ; Online: Innovative Toolbox for the Quantification of Drosophila C Virus, Drosophila A Virus, and Nora Virus.

Nigg, Jared C / Mongelli, Vanesa / Blanc, Hervé / Saleh, Maria-Carla

Journal of molecular biology

2021 Volume 434, Issue 6, Page(s) 167308

Abstract: ... In Drosophila melanogaster, persistent infections with Drosophila C virus, Drosophila A virus, and Nora virus are commonly ... of Drosophila C virus infection that allows quantification of infectious titers for a wider range of Drosophila ... C virus isolates. We also describe strand specific RT-qPCR assays for quantification of viral ...

Abstract	Quantification of viral replication underlies investigations into host-virus interactions. In Drosophila melanogaster, persistent infections with Drosophila C virus, Drosophila A virus, and Nora virus are commonly observed in nature and in laboratory fly stocks. However, traditional endpoint dilution assays to quantify infectious titers are not compatible with persistently infecting isolates of these viruses that do not cause cytopathic effects in cell culture. Here we present a novel assay based on immunological detection of Drosophila C virus infection that allows quantification of infectious titers for a wider range of Drosophila C virus isolates. We also describe strand specific RT-qPCR assays for quantification of viral negative strand RNA produced during Drosophila C virus, Drosophila A virus, and Nora virus infection. Finally, we demonstrate the utility of these assays for quantification of viral replication during oral infections and persistent infections with each virus.
MeSH term(s)	Animals ; Dicistroviridae/isolation & purification ; Dicistroviridae/physiology ; Drosophila melanogaster/virology ; Immunoassay ; RNA, Viral/genetics ; Real-Time Polymerase Chain Reaction ; Virus Replication
Chemical Substances	RNA, Viral
Language	English
Publishing date	2021-10-19
Publishing country	Netherlands
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	80229-3
ISSN	1089-8638 ; 0022-2836
ISSN (online)	1089-8638
ISSN	0022-2836
DOI	10.1016/j.jmb.2021.167308
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Article: An Adaptable Platform for in-house Hepatitis C Serology

Journal of virological methods. 2022 July 14,

2022

Abstract: ... an adaptable enzyme-linked immunoassay (ELISA) using hepatitis C virus (HCV) as a proof-of-concept application ...

Abstract	Serology-based diagnosis remains one of the major tools for diagnosis and surveillance of infectious diseases. However, for many neglected diseases no or only few commercial assays are available and often with prices prohibiting large scale testing in low and middle-income countries (LMICs). We developed an adaptable enzyme-linked immunoassay (ELISA) using hepatitis C virus (HCV) as a proof-of-concept application. By combining the maltose-binding-protein with a multiepitope HCV protein, we were able to obtain a high concentration of protein suitable for downstream applications. Following optimization, the assay was verified using previously tested human samples from Canada, Denmark and Gabon in parallel with the use of a commercial protein. Sensitivity and specificity were calculated to 98% and 97% respectively, after accounting for non-specific binding and assay optimization. This study provides a thorough description of the development, and validation of a multiepitope ELISA-based diagnostic assay against HCV, which could be implemented at low cost. The described methodology can be readily adapted to develop novel ELISA-based diagnostic assays for other infectious pathogens with well-described immunogenic epitopes. This method could improve the diagnosis of neglected diseases for which affordable diagnostic assays are lacking.
Keywords	Hepatitis C virus ; enzyme-linked immunosorbent assay ; epitopes ; hepatitis C ; humans ; monitoring ; serology ; Canada ; Denmark ; Gabon
Language	English
Dates of publication	2022-0714
Publishing place	Elsevier B.V.
Document type	Article
Note	Pre-press version
ZDB-ID	8013-5
ISSN	1879-0984 ; 0166-0934
ISSN (online)	1879-0984
ISSN	0166-0934
DOI	10.1016/j.jviromet.2022.114586
Database	NAL-Catalogue (AGRICOLA)

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Article ; Online: Correction: Effects of Vitellaria paradoxa (C.F. Gaertn.) Aqueous leaf extract administration on Salmonella typhimurium-infected rats.

Fodouop, Siméon Pierre Chegaing / Tala, Sedric Donald / Keilah, Lunga Paul / Kodjio, Norbert / Yemele, Mefokou Didiane / Nwabo Kamdje, Armel Herve / Nji-Kah, Bridget / Tchoumboue, Joseph / Gatsing, Donatien

BMC complementary medicine and therapies

2023 Volume 23, Issue 1, Page(s) 40

Language	English
Publishing date	2023-02-07
Publishing country	England
Document type	Published Erratum
ISSN	2662-7671
ISSN (online)	2662-7671
DOI	10.1186/s12906-023-03846-8
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Article ; Online: Observation of the B_{c}^{+} Meson in Pb-Pb and pp Collisions at sqrt[s_{NN}]=5.02 TeV and Measurement of its Nuclear Modification Factor.

Tumasyan, A / Adam, W / Andrejkovic, J W / Bergauer, T / Chatterjee, S / Dragicevic, M / Del Valle, A Escalante / Frühwirth, R / Jeitler, M / Krammer, N / Lechner, L / Liko, D / Mikulec, I / Paulitsch, P / Pitters, F M / Schieck, J / Schöfbeck, R / Schwarz, D / Templ, S /

Waltenberger, W / Wulz, C-E / Chekhovsky, V / Litomin, A / Makarenko, V / Darwish, M R / De Wolf, E A / Janssen, T / Kello, T / Lelek, A / Sfar, H Rejeb / Van Mechelen, P / Van Putte, S / Van Remortel, N / Blekman, F / Bols, E S / D'Hondt, J / Delcourt, M / Faham, H El / Lowette, S / Moortgat, S / Morton, A / Müller, D / Sahasransu, A R / Tavernier, S / Van Doninck, W / Van Mulders, P / Beghin, D / Bilin, B / Clerbaux, B / De Lentdecker, G / Favart, L / Grebenyuk, A / Kalsi, A K / Lee, K / Mahdavikhorrami, M / Makarenko, I / Moureaux, L / Pétré, L / Popov, A / Postiau, N / Starling, E / Thomas, L / Vanden Bemden, M / Vander Velde, C / Vanlaer, P / Wezenbeek, L / Cornelis, T / Dobur, D / Knolle, J / Lambrecht, L / Mestdach, G / Niedziela, M / Roskas, C / Samalan, A / Skovpen, K / Tytgat, M / Vermassen, B / Vit, M / Benecke, A / Bethani, A / Bruno, G / Bury, F / Caputo, C / David, P / Delaere, C / Donertas, I S / Giammanco, A / Jaffel, K / Jain, Sa / Lemaitre, V / Mondal, K / Prisciandaro, J / Taliercio, A / Teklishyn, M / Tran, T T / Vischia, P / Wertz, S / Alves, G A / Hensel, C / Moraes, A / Júnior, W L Aldá / Pereira, M Alves Gallo / Filho, M Barroso Ferreira / Malbouisson, H Brandao / Carvalho, W / Chinellato, J / Da Costa, E M / Da Silveira, G G / Damiao, D De Jesus / De Souza, S Fonseca / Figueiredo, D Matos / Herrera, C Mora / Amarilo, K Mota / Mundim, L / Nogima, H / Teles, P Rebello / Santoro, A / Amaral, S M Silva Do / Sznajder, A / Thiel, M / De Araujo, F Torres Da Silva / Pereira, A Vilela / Bernardes, C A / Calligaris, L / Tomei, T R Fernandez Perez / Gregores, E M / Lemos, D S / Mercadante, P G / Novaes, S F / Padula, Sandra S / Aleksandrov, A / Antchev, G / Hadjiiska, R / Iaydjiev, P / Misheva, M / Rodozov, M / Shopova, M / Sultanov, G / Dimitrov, A / Ivanov, T / Litov, L / Pavlov, B / Petkov, P / Petrov, A / Cheng, T / Javaid, T / Mittal, M / Yuan, L / Ahmad, M / Bauer, G / Dozen, C / Hu, Z / Martins, J / Wang, Y / Yi, K / Chapon, E / Chen, G M / Chen, H S / Chen, M / Iemmi, F / Kapoor, A / Leggat, D / Liao, H / Liu, Z-A / Milosevic, V / Monti, F / Sharma, R / Tao, J / Thomas-Wilsker, J / Wang, J / Zhang, H / Zhao, J / Agapitos, A / An, Y / Ban, Y / Chen, C / Levin, A / Li, Q / Lyu, X / Mao, Y / Qian, S J / Wang, D / Wang, Q / Xiao, J / Lu, M / You, Z / Gao, X / Okawa, H / Lin, Z / Xiao, M / Avila, C / Cabrera, A / Florez, C / Fraga, J / Guisao, J Mejia / Ramirez, F / Alvarez, J D Ruiz / González, C A Salazar / Giljanovic, D / Godinovic, N / Lelas, D / Puljak, I / Antunovic, Z / Kovac, M / Sculac, T / Brigljevic, V / Ferencek, D / Majumder, D / Roguljic, M / Starodumov, A / Susa, T / Attikis, A / Christoforou, K / Erodotou, E / Ioannou, A / Kole, G / Kolosova, M / Konstantinou, S / Mousa, J / Nicolaou, C / Ptochos, F / Razis, P A / Rykaczewski, H / Saka, H / Finger, M / Kveton, A / Ayala, E / Jarrin, E Carrera / Elgammal, S / Kamel, A Ellithi / Mahmoud, M A / Mohammed, Y / Bhowmik, S / Dewanjee, R K / Ehataht, K / 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Physical review letters

2022 Volume 128, Issue 25, Page(s) 252301

Abstract: The B_{c}^{+} meson is observed for the first time in heavy ion collisions. Data from the CMS ... detector are used to study the production of the B_{c}^{+} meson in lead-lead (Pb-Pb) and proton-proton (pp ... collisions at a center-of-mass energy per nucleon pair of sqrt[s_{NN}]=5.02 TeV, via the B_{c}^{+}→(J/ψ→μ^ ...

Abstract	The B_{c}^{+} meson is observed for the first time in heavy ion collisions. Data from the CMS detector are used to study the production of the B_{c}^{+} meson in lead-lead (Pb-Pb) and proton-proton (pp) collisions at a center-of-mass energy per nucleon pair of sqrt[s_{NN}]=5.02 TeV, via the B_{c}^{+}→(J/ψ→μ^{+}μ^{-})μ^{+}ν_{μ} decay. The B_{c}^{+} nuclear modification factor, derived from the Pb-Pb-to-pp ratio of production cross sections, is measured in two bins of the trimuon transverse momentum and of the Pb-Pb collision centrality. The B_{c}^{+} meson is shown to be less suppressed than quarkonia and most of the open heavy-flavor mesons, suggesting that effects of the hot and dense nuclear matter created in heavy ion collisions contribute to its production. This measurement sets forth a promising new probe of the interplay of suppression and enhancement mechanisms in the production of heavy-flavor mesons in the quark-gluon plasma.
Language	English
Publishing date	2022-06-27
Publishing country	United States
Document type	Journal Article
ZDB-ID	208853-8
ISSN	1079-7114 ; 0031-9007
ISSN (online)	1079-7114
ISSN	0031-9007
DOI	10.1103/PhysRevLett.128.252301
Database	MEDical Literature Analysis and Retrieval System OnLINE

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