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  1. Article ; Online: Considerations for the discovery and development of 3-chymotrypsin-like cysteine protease inhibitors targeting SARS-CoV-2 infection.

    Vandyck, Koen / Deval, Jerome

    Current opinion in virology

    2021  Volume 49, Page(s) 36–40

    Abstract: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the cause of the COVID-19 pandemic. The coronavirus 3-chymotrypsin-like protease (3CLpro) controls virus replication and is therefore considered a major target and promising opportunity for ... ...

    Abstract Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the cause of the COVID-19 pandemic. The coronavirus 3-chymotrypsin-like protease (3CLpro) controls virus replication and is therefore considered a major target and promising opportunity for rational-based antiviral discovery with direct acting agents. Here we review first-generation SARS-CoV-2 3CLpro inhibitors PF-07304814, GC-376, and CDI-45205 that are being delivered either by injection or inhalation due to their low intrinsic oral bioavailability. In addition, PF-07321332 is now emerging as a promising second-generation clinical candidate for oral delivery. A key challenge to the development of novel 3CLpro inhibitors is the poor understanding of the predictive value of in vitro potency toward clinical efficacy, an issue complicated by the involvement of host proteases in virus entry. Further preclinical and clinical validation will be key to establishing 3CLpro inhibitors as a bona fide class for future SARS-CoV-2 therapeutics for both hospitalized and outpatient populations.
    MeSH term(s) Animals ; Antiviral Agents/chemistry ; Antiviral Agents/pharmacology ; Antiviral Agents/therapeutic use ; COVID-19/drug therapy ; Coronavirus 3C Proteases/antagonists & inhibitors ; Cysteine Proteinase Inhibitors/chemistry ; Cysteine Proteinase Inhibitors/pharmacology ; Cysteine Proteinase Inhibitors/therapeutic use ; Drug Administration Routes ; Drug Development ; Drug Discovery ; Humans ; SARS-CoV-2/drug effects ; SARS-CoV-2/enzymology
    Chemical Substances Antiviral Agents ; Cysteine Proteinase Inhibitors ; 3C-like proteinase, SARS-CoV-2 (EC 3.4.22.-) ; Coronavirus 3C Proteases (EC 3.4.22.28)
    Language English
    Publishing date 2021-04-27
    Publishing country Netherlands
    Document type Journal Article ; Review
    ZDB-ID 2611378-8
    ISSN 1879-6265 ; 1879-6257
    ISSN (online) 1879-6265
    ISSN 1879-6257
    DOI 10.1016/j.coviro.2021.04.006
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Antiviral Properties and Mechanism of Action Studies of the Hepatitis B Virus Capsid Assembly Modulator JNJ-56136379.

    Berke, Jan Martin / Dehertogh, Pascale / Vergauwen, Karen / Mostmans, Wendy / Vandyck, Koen / Raboisson, Pierre / Pauwels, Frederik

    Antimicrobial agents and chemotherapy

    2020  Volume 64, Issue 5

    Abstract: Capsid assembly is a critical step in the hepatitis B virus (HBV) life cycle, mediated by the core protein. Core is a potential target for new antiviral therapies, the capsid assembly modulators (CAMs). JNJ-56136379 (JNJ-6379) is a novel and potent CAM ... ...

    Abstract Capsid assembly is a critical step in the hepatitis B virus (HBV) life cycle, mediated by the core protein. Core is a potential target for new antiviral therapies, the capsid assembly modulators (CAMs). JNJ-56136379 (JNJ-6379) is a novel and potent CAM currently in phase II trials. We evaluated the mechanisms of action (MOAs) and antiviral properties of JNJ-6379
    MeSH term(s) Antiviral Agents/pharmacology ; Capsid/drug effects ; Capsid/ultrastructure ; Capsid Proteins/metabolism ; Cell Line ; DNA Replication/drug effects ; DNA, Viral/biosynthesis ; DNA, Viral/drug effects ; Dose-Response Relationship, Drug ; Drug Synergism ; Hepatitis B/drug therapy ; Hepatitis B/virology ; Hepatitis B virus/drug effects ; Hepatitis B virus/ultrastructure ; Hepatocytes/virology ; Humans ; Microbial Sensitivity Tests ; Organic Chemicals/pharmacology ; Primary Cell Culture ; Virus Replication/drug effects
    Chemical Substances Antiviral Agents ; Capsid Proteins ; DNA, Viral ; JNJ-56136379 ; Organic Chemicals
    Language English
    Publishing date 2020-04-21
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 217602-6
    ISSN 1098-6596 ; 0066-4804
    ISSN (online) 1098-6596
    ISSN 0066-4804
    DOI 10.1128/AAC.02439-19
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: The Substitutions L50F, E166A, and L167F in SARS-CoV-2 3CLpro Are Selected by a Protease Inhibitor

    Jochmans, Dirk / Liu, Cheng / Donckers, Kim / Stoycheva, Antitsa / Boland, Sandro / Stevens, Sarah K / De Vita, Chloe / Vanmechelen, Bert / Maes, Piet / Trüeb, Bettina / Ebert, Nadine / Thiel, Volker / De Jonghe, Steven / Vangeel, Laura / Bardiot, Dorothée / Jekle, Andreas / Blatt, Lawrence M / Beigelman, Leonid / Symons, Julian A /
    Raboisson, Pierre / Chaltin, Patrick / Marchand, Arnaud / Neyts, Johan / Deval, Jerome / Vandyck, Koen

    mBio

    2023  Volume 14, Issue 1, Page(s) e0281522

    Abstract: The SARS-CoV-2 main protease (3CLpro) has an indispensable role in the viral life cycle and is a therapeutic target for the treatment of COVID-19. The potential of 3CLpro-inhibitors to select for drug-resistant variants needs to be established. Therefore, ...

    Abstract The SARS-CoV-2 main protease (3CLpro) has an indispensable role in the viral life cycle and is a therapeutic target for the treatment of COVID-19. The potential of 3CLpro-inhibitors to select for drug-resistant variants needs to be established. Therefore, SARS-CoV-2 was passaged
    MeSH term(s) Humans ; Antiviral Agents/pharmacology ; Antiviral Agents/chemistry ; COVID-19 ; Enzyme Inhibitors ; Protease Inhibitors/pharmacology ; Protease Inhibitors/chemistry ; SARS-CoV-2/genetics
    Chemical Substances Antiviral Agents ; ensitrelvir (PX665RAA3H) ; Enzyme Inhibitors ; nirmatrelvir and ritonavir drug combination ; Protease Inhibitors ; 3C-like proteinase, SARS-CoV-2 (EC 3.4.22.-)
    Language English
    Publishing date 2023-01-10
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2557172-2
    ISSN 2150-7511 ; 2161-2129
    ISSN (online) 2150-7511
    ISSN 2161-2129
    DOI 10.1128/mbio.02815-22
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  4. Article ; Online: Correction to: Pharmacokinetics, Safety and Tolerability of JNJ-56136379, a Novel Hepatitis B Virus Capsid Assembly Modulator, in Healthy Subjects.

    Vandenbossche, Joris / Jessner, Wolfgang / van den Boer, Maarten / Biewenga, Jeike / Berke, Jan Martin / Talloen, Willem / De Zwart, Loeckie / Snoeys, Jan / Vandyck, Koen / Fry, John / Yogaratnam, Jeysen

    Advances in therapy

    2020  Volume 37, Issue 4, Page(s) 1703

    Abstract: ... Martin Berke, Willem Talloen, Loeckie De Zwart, Jan Snoeys, Koen Vandyck, John Fry, Jeysen Yogaratnam. ...

    Abstract In the original article Ninth and Tenth authors were incorrectly omitted from the author group. The correct author group is Joris Vandenbossche, Wolfgang Jessner, Maarten van den Boer, Jeike Biewenga, Jan Martin Berke, Willem Talloen, Loeckie De Zwart, Jan Snoeys, Koen Vandyck, John Fry, Jeysen Yogaratnam.
    Language English
    Publishing date 2020-02-18
    Publishing country United States
    Document type Published Erratum
    ZDB-ID 632651-1
    ISSN 1865-8652 ; 0741-238X
    ISSN (online) 1865-8652
    ISSN 0741-238X
    DOI 10.1007/s12325-020-01249-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Development of a cellular high-content, immunofluorescent HBV core assay to identify novel capsid assembly modulators that induce the formation of aberrant HBV core structures.

    Sauviller, Sarah / Vergauwen, Karen / Jaensch, Steffen / Gustin, Emmanuel / Peeters, Danielle / Vermeulen, Peter / Wuyts, Dirk / Vandyck, Koen / Pauwels, Frederik / Berke, Jan Martin

    Journal of virological methods

    2021  Volume 293, Page(s) 114150

    Abstract: Hepatitis B Virus (HBV) core protein has multiple functions in the viral life cycle and is an attractive target for new anti-viral therapies. Capsid assembly modulators (CAMs) target the core protein and induce the formation of either morphologically ... ...

    Abstract Hepatitis B Virus (HBV) core protein has multiple functions in the viral life cycle and is an attractive target for new anti-viral therapies. Capsid assembly modulators (CAMs) target the core protein and induce the formation of either morphologically normal (CAM-N) or aberrant structures (CAM-A), both devoid of genomic material. To date a diverse family of CAM-N chemotypes has been identified, but in contrast, described CAM-As are based on the heteroaryldihydropyrimidine (HAP) scaffold. We used the HBV-inducible HepG2.117 cell line with immunofluorescent labeling of HBV core to develop and validate a cellular high-content image-based assay where aggregated core structures are identified using image analysis spot texture features. Treatment with HAPs led to a dose- and time-dependent formation of aggregated core appearing as dot-like structures in the cytoplasm and nucleus. By combining a biochemical and cellular screening approach, a compound was identified as a novel non-HAP scaffold able to induce dose-dependent formation of aberrant core structures, which was confirmed by electron microscopy and native gel electrophoresis. This compound displayed anti-HBV activity in HepG2.117 cells, providing proof-of-concept for our screening approach. We believe our combined biochemical and cellular high-content screening method will aid in expanding the range of CAM-A chemotypes.
    MeSH term(s) Capsid ; Hepatitis B virus ; Pyrimidines ; Virus Assembly ; Virus Replication
    Chemical Substances Pyrimidines ; heteroaryldihydropyrimidine
    Language English
    Publishing date 2021-04-08
    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.2021.114150
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Dual inhibition of SARS-CoV-2 and human rhinovirus with protease inhibitors in clinical development.

    Liu, Cheng / Boland, Sandro / Scholle, Michael D / Bardiot, Dorothee / Marchand, Arnaud / Chaltin, Patrick / Blatt, Lawrence M / Beigelman, Leonid / Symons, Julian A / Raboisson, Pierre / Gurard-Levin, Zachary A / Vandyck, Koen / Deval, Jerome

    Antiviral research

    2021  Volume 187, Page(s) 105020

    Abstract: The 3-chymotrypsin-like cysteine protease (3CLpro) of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is considered a major target for the discovery of direct antiviral agents. We previously reported the evaluation of SARS-CoV-2 3CLpro ... ...

    Abstract The 3-chymotrypsin-like cysteine protease (3CLpro) of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is considered a major target for the discovery of direct antiviral agents. We previously reported the evaluation of SARS-CoV-2 3CLpro inhibitors in a novel self-assembled monolayer desorption ionization mass spectrometry (SAMDI-MS) enzymatic assay (Gurard-Levin et al., 2020). The assay was further improved by adding the rhinovirus HRV3C protease to the same well as the SARS-CoV-2 3CLpro enzyme. High substrate specificity for each enzyme allowed the proteases to be combined in a single assay reaction without interfering with their individual activities. This novel duplex assay was used to profile a diverse set of reference protease inhibitors. The protease inhibitors were grouped into three categories based on their relative potency against 3CLpro and HRV3C including those that are: equipotent against 3CLpro and HRV3C (GC376 and calpain inhibitor II), selective for 3CLpro (PF-00835231, calpain inhibitor XII, boceprevir), and selective for HRV3C (rupintrivir). Structural analysis showed that the combination of minimal interactions, conformational flexibility, and limited bulk allows GC376 and calpain inhibitor II to potently inhibit both enzymes. In contrast, bulkier compounds interacting more tightly with pockets P2, P3, and P4 due to optimization for a specific target display a more selective inhibition profile. Consistently, the most selective viral protease inhibitors were relatively weak inhibitors of human cathepsin L. Taken together, these results can guide the design of cysteine protease inhibitors that are either virus-specific or retain a broad antiviral spectrum against coronaviruses and rhinoviruses.
    MeSH term(s) Antiviral Agents/chemistry ; Antiviral Agents/pharmacology ; Binding Sites ; Cathepsin L/metabolism ; Coronavirus 3C Proteases/antagonists & inhibitors ; Drug Discovery ; Glycoproteins/pharmacology ; Humans ; Kinetics ; Models, Molecular ; Protease Inhibitors/chemistry ; Protease Inhibitors/pharmacology ; Pyrrolidines/pharmacology ; Rhinovirus/drug effects ; SARS-CoV-2/drug effects ; Sulfonic Acids
    Chemical Substances Antiviral Agents ; Glycoproteins ; Protease Inhibitors ; Pyrrolidines ; Sulfonic Acids ; calpain inhibitors ; CTSL protein, human (EC 3.4.22.15) ; Cathepsin L (EC 3.4.22.15) ; Coronavirus 3C Proteases (EC 3.4.22.28) ; GC376 (H1NMJ5XDG5)
    Language English
    Publishing date 2021-01-27
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 306628-9
    ISSN 1872-9096 ; 0166-3542
    ISSN (online) 1872-9096
    ISSN 0166-3542
    DOI 10.1016/j.antiviral.2021.105020
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  7. Article ; Online: Novel Potent Capsid Assembly Modulators Regulate Multiple Steps of the Hepatitis B Virus Life Cycle.

    Lahlali, Thomas / Berke, Jan Martin / Vergauwen, Karen / Foca, Adrien / Vandyck, Koen / Pauwels, Frederik / Zoulim, Fabien / Durantel, David

    Antimicrobial agents and chemotherapy

    2018  Volume 62, Issue 10

    Abstract: The assembly of hepatitis B virus (HBV) core protein (HBc) into capsids represents a critical step of viral replication. HBc has multiple functions during the HBV life cycle, which makes it an attractive target for antiviral therapies. Capsid assembly ... ...

    Abstract The assembly of hepatitis B virus (HBV) core protein (HBc) into capsids represents a critical step of viral replication. HBc has multiple functions during the HBV life cycle, which makes it an attractive target for antiviral therapies. Capsid assembly modulators (CAMs) induce the formation of empty capsid or aberrant capsid devoid of pregenomic RNA (pgRNA) and finally block relaxed circular DNA neosynthesis and virion progeny. In this study, the novel CAMs JNJ-827 and JNJ-890 were found to be potent inhibitors of HBV replication with respective half-maximal effective concentrations of 4.7 and 66 nM, respectively, in HepG2.117 cells. Antiviral profiling in differentiated HepaRG (dHepaRG) cells and primary human hepatocytes revealed that these compounds efficiently inhibited HBV replication, as well as
    MeSH term(s) Antiviral Agents/pharmacology ; Capsid/drug effects ; Capsid/metabolism ; Capsid Proteins/genetics ; Capsid Proteins/metabolism ; Cell Line, Tumor ; DNA, Circular/genetics ; DNA, Circular/metabolism ; Hep G2 Cells ; Hepatitis B Surface Antigens/genetics ; Hepatitis B Surface Antigens/metabolism ; Hepatitis B e Antigens ; Hepatitis B virus/drug effects ; Hepatitis B virus/metabolism ; Hepatitis B virus/pathogenicity ; Hepatocytes/virology ; Humans ; RNA, Viral/genetics ; RNA, Viral/metabolism ; Virus Assembly/drug effects ; Virus Assembly/genetics ; Virus Replication/drug effects ; Virus Replication/genetics
    Chemical Substances Antiviral Agents ; Capsid Proteins ; DNA, Circular ; Hepatitis B Surface Antigens ; Hepatitis B e Antigens ; RNA, Viral
    Language English
    Publishing date 2018-09-24
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 217602-6
    ISSN 1098-6596 ; 0066-4804
    ISSN (online) 1098-6596
    ISSN 0066-4804
    DOI 10.1128/AAC.00835-18
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  8. Article ; Online: Capsid Assembly Modulators Have a Dual Mechanism of Action in Primary Human Hepatocytes Infected with Hepatitis B Virus.

    Berke, Jan Martin / Dehertogh, Pascale / Vergauwen, Karen / Van Damme, Ellen / Mostmans, Wendy / Vandyck, Koen / Pauwels, Frederik

    Antimicrobial agents and chemotherapy

    2017  Volume 61, Issue 8

    Abstract: Hepatitis B virus (HBV) capsid assembly is a critical step in the propagation of the virus and is mediated by the core protein. Due to its multiple functions in the viral life cycle, core became an attractive target for new antiviral therapies. Capsid ... ...

    Abstract Hepatitis B virus (HBV) capsid assembly is a critical step in the propagation of the virus and is mediated by the core protein. Due to its multiple functions in the viral life cycle, core became an attractive target for new antiviral therapies. Capsid assembly modulators (CAMs) accelerate the kinetics of capsid assembly and prevent encapsidation of the polymerase-pregenomic RNA (Pol-pgRNA) complex, thereby blocking viral replication. CAM JNJ-632 is a novel and potent inhibitor of HBV replication
    Language English
    Publishing date 2017-08
    Publishing country United States
    Document type Journal Article
    ZDB-ID 217602-6
    ISSN 1098-6596 ; 0066-4804
    ISSN (online) 1098-6596
    ISSN 0066-4804
    DOI 10.1128/AAC.00560-17
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  9. Article ; Online: Evaluation of SARS-CoV-2 3C-like protease inhibitors using self-assembled monolayer desorption ionization mass spectrometry.

    Gurard-Levin, Zachary A / Liu, Cheng / Jekle, Andreas / Jaisinghani, Ruchika / Ren, Suping / Vandyck, Koen / Jochmans, Dirk / Leyssen, Pieter / Neyts, Johan / Blatt, Lawrence M / Beigelman, Leonid / Symons, Julian A / Raboisson, Pierre / Scholle, Michael D / Deval, Jerome

    Antiviral research

    2020  Volume 182, Page(s) 104924

    Abstract: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the cause of the COVID-19 pandemic that began in 2019. The coronavirus 3-chymotrypsin-like cysteine protease (3CLpro) controls replication and is therefore considered a major target for ... ...

    Abstract Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the cause of the COVID-19 pandemic that began in 2019. The coronavirus 3-chymotrypsin-like cysteine protease (3CLpro) controls replication and is therefore considered a major target for antiviral discovery. This study describes the evaluation of SARS-CoV-2 3CLpro inhibitors in a novel self-assembled monolayer desorption ionization mass spectrometry (SAMDI-MS) enzymatic assay. Compared with a traditional FRET readout, the label-free SAMDI-MS assay offers greater sensitivity and eliminates false positive inhibition from compound interference with the optical signal. The SAMDI-MS assay was optimized and validated with known inhibitors of coronavirus 3CLpro such as GC376 (IC
    MeSH term(s) Antiviral Agents/pharmacology ; Betacoronavirus/drug effects ; Betacoronavirus/enzymology ; COVID-19 ; Coronavirus 3C Proteases ; Coronavirus Infections/drug therapy ; Coronavirus Infections/virology ; Cysteine Endopeptidases/chemistry ; Cysteine Endopeptidases/metabolism ; Cysteine Proteinase Inhibitors/chemistry ; Cysteine Proteinase Inhibitors/pharmacology ; Glycoproteins/pharmacology ; HeLa Cells ; Humans ; Pandemics ; Pneumonia, Viral/drug therapy ; Pneumonia, Viral/virology ; SARS-CoV-2 ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization/methods ; Viral Nonstructural Proteins/antagonists & inhibitors ; Viral Nonstructural Proteins/chemistry ; Viral Nonstructural Proteins/metabolism
    Chemical Substances Antiviral Agents ; Cysteine Proteinase Inhibitors ; Glycoproteins ; Viral Nonstructural Proteins ; Cysteine Endopeptidases (EC 3.4.22.-) ; Coronavirus 3C Proteases (EC 3.4.22.28)
    Keywords covid19
    Language English
    Publishing date 2020-09-05
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 306628-9
    ISSN 1872-9096 ; 0166-3542
    ISSN (online) 1872-9096
    ISSN 0166-3542
    DOI 10.1016/j.antiviral.2020.104924
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  10. Article ; Online: ALG-097111, a potent and selective SARS-CoV-2 3-chymotrypsin-like cysteine protease inhibitor exhibits in vivo efficacy in a Syrian Hamster model.

    Vandyck, Koen / Abdelnabi, Rana / Gupta, Kusum / Jochmans, Dirk / Jekle, Andreas / Deval, Jerome / Misner, Dinah / Bardiot, Dorothée / Foo, Caroline S / Liu, Cheng / Ren, Suping / Beigelman, Leonid / Blatt, Lawrence M / Boland, Sandro / Vangeel, Laura / Dejonghe, Steven / Chaltin, Patrick / Marchand, Arnaud / Serebryany, Vladimir /
    Stoycheva, Antitsa / Chanda, Sushmita / Symons, Julian A / Raboisson, Pierre / Neyts, Johan

    Biochemical and biophysical research communications

    2021  Volume 555, Page(s) 134–139

    Abstract: There is an urgent need for antivirals targeting the SARS-CoV-2 virus to fight the current COVID-19 pandemic. The SARS-CoV-2 main protease (3CLpro) represents a promising target for antiviral therapy. The lack of selectivity for some of the reported ... ...

    Abstract There is an urgent need for antivirals targeting the SARS-CoV-2 virus to fight the current COVID-19 pandemic. The SARS-CoV-2 main protease (3CLpro) represents a promising target for antiviral therapy. The lack of selectivity for some of the reported 3CLpro inhibitors, specifically versus cathepsin L, raises potential safety and efficacy concerns. ALG-097111 potently inhibited SARS-CoV-2 3CLpro (IC
    MeSH term(s) Amides/pharmacokinetics ; Amides/pharmacology ; Animals ; COVID-19/drug therapy ; COVID-19/virology ; Cathepsin L/antagonists & inhibitors ; Cell Line ; Coronavirus 3C Proteases/antagonists & inhibitors ; Cricetinae ; Cysteine Proteinase Inhibitors/pharmacokinetics ; Cysteine Proteinase Inhibitors/pharmacology ; Disease Models, Animal ; Female ; Humans ; Inhibitory Concentration 50 ; Male ; Mesocricetus/virology ; Reproducibility of Results ; SARS-CoV-2/drug effects ; SARS-CoV-2/enzymology ; SARS-CoV-2/growth & development ; Serine Endopeptidases ; Substrate Specificity ; Virus Replication/drug effects
    Chemical Substances ALG-097111 ; Amides ; Cysteine Proteinase Inhibitors ; Serine Endopeptidases (EC 3.4.21.-) ; TMPRSS2 protein, human (EC 3.4.21.-) ; Cathepsin L (EC 3.4.22.15) ; Coronavirus 3C Proteases (EC 3.4.22.28)
    Language English
    Publishing date 2021-03-26
    Publishing country United States
    Document type Journal Article
    ZDB-ID 205723-2
    ISSN 1090-2104 ; 0006-291X ; 0006-291X
    ISSN (online) 1090-2104 ; 0006-291X
    ISSN 0006-291X
    DOI 10.1016/j.bbrc.2021.03.096
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