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  1. Article ; Online: gP2S, an Information Management System for CryoEM Experiments.

    Wypych, Dorota / Kierecki, Daniel / Golebiowski, Filip M / Rohou, Alexis

    Journal of visualized experiments : JoVE

    2021  , Issue 172

    Abstract: Cryogenic electron microscopy (cryoEM) has become an integral part of many drug-discovery projects because crystallography of the protein target is not always achievable and cryoEM provides an alternative means to support structure-based ligand design. ... ...

    Abstract Cryogenic electron microscopy (cryoEM) has become an integral part of many drug-discovery projects because crystallography of the protein target is not always achievable and cryoEM provides an alternative means to support structure-based ligand design. When dealing with a large number of distinct projects, and within each project a potentially large number of ligand-protein co-structures, accurate record keeping rapidly becomes challenging. Many experimental parameters are tuned for each target, including at the sample preparation, grid preparation, and microscopy stages. Therefore, accurate record keeping can be crucially important to enable long-term reproducibility, and to facilitate efficient teamwork, especially when steps of the cryoEM workflow are performed by different operators. To help deal with this challenge, we developed a web-based information management system for cryoEM, called gP2S. The application keeps track of each experiment, from sample to final atomic model, in the context of projects, a list of which is maintained in the application, or externally in a separate system. User-defined controlled vocabularies of consumables, equipment, protocols and software help describe each step of the cryoEM workflow in a structured manner. gP2S is widely configurable and, depending on the team's needs, may exist as a standalone product or be a part of a broader ecosystem of scientific applications, integrating via REST APIs with project management tools, applications tracking the production of proteins or of small molecules ligands, or applications automating data collection and storage. Users can register details of each grid and microscopy session including key experimental metadata and parameter values, and the lineage of each experimental artifact (sample, grid, microscopy session, map, etc.) is recorded. gP2S serves as a cryoEM experimental workflow organizer that enables accurate record keeping for teams, and is available under an open-source license.
    MeSH term(s) Cryoelectron Microscopy ; Ecosystem ; Information Management ; Reproducibility of Results ; Software
    Language English
    Publishing date 2021-06-10
    Publishing country United States
    Document type Journal Article ; Video-Audio Media
    ZDB-ID 2259946-0
    ISSN 1940-087X ; 1940-087X
    ISSN (online) 1940-087X
    ISSN 1940-087X
    DOI 10.3791/62377
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Lesion recognition by XPC, TFIIH and XPA in DNA excision repair.

    Kim, Jinseok / Li, Chia-Lung / Chen, Xuemin / Cui, Yanxiang / Golebiowski, Filip M / Wang, Huaibin / Hanaoka, Fumio / Sugasawa, Kaoru / Yang, Wei

    Nature

    2023  Volume 617, Issue 7959, Page(s) 170–175

    Abstract: Nucleotide excision repair removes DNA lesions caused by ultraviolet light, cisplatin-like compounds and bulky ... ...

    Abstract Nucleotide excision repair removes DNA lesions caused by ultraviolet light, cisplatin-like compounds and bulky adducts
    MeSH term(s) Humans ; DNA/chemistry ; DNA/metabolism ; DNA Damage ; DNA Helicases/metabolism ; DNA Repair ; DNA-Binding Proteins/metabolism ; Transcription Factor TFIIH/metabolism ; Xeroderma Pigmentosum Group A Protein/metabolism ; Substrate Specificity ; DNA-Directed RNA Polymerases/metabolism
    Chemical Substances DNA (9007-49-2) ; DNA Helicases (EC 3.6.4.-) ; DNA-Binding Proteins ; Transcription Factor TFIIH (148710-81-0) ; Xeroderma Pigmentosum Group A Protein ; XPA protein, human ; XPC protein, human (156533-34-5) ; ERCC2 protein, human (EC 5.99.-) ; DNA-Directed RNA Polymerases (EC 2.7.7.6)
    Language English
    Publishing date 2023-04-19
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Intramural
    ZDB-ID 120714-3
    ISSN 1476-4687 ; 0028-0836
    ISSN (online) 1476-4687
    ISSN 0028-0836
    DOI 10.1038/s41586-023-05959-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Gp2s, an information management system for cryoem experiments

    Wypych, Dorota / Kierecki, Daniel / Golebiowski, Filip M / Rohou, Alexis

    Journal of visualized experiments. 2021 June 10, , no. 172

    2021  

    Abstract: Cryogenic electron microscopy (cryoEM) has become an integral part of many drug-discovery projects because crystallography of the protein target is not always achievable and cryoEM provides an alternative means to support structure-based ligand design. ... ...

    Abstract Cryogenic electron microscopy (cryoEM) has become an integral part of many drug-discovery projects because crystallography of the protein target is not always achievable and cryoEM provides an alternative means to support structure-based ligand design. When dealing with a large number of distinct projects, and within each project a potentially large number of ligand-protein co-structures, accurate record keeping rapidly becomes challenging. Many experimental parameters are tuned for each target, including at the sample preparation, grid preparation, and microscopy stages. Therefore, accurate record keeping can be crucially important to enable long-term reproducibility, and to facilitate efficient teamwork, especially when steps of the cryoEM workflow are performed by different operators. To help deal with this challenge, we developed a web-based information management system for cryoEM, called gP2S. The application keeps track of each experiment, from sample to final atomic model, in the context of projects, a list of which is maintained in the application, or externally in a separate system. User-defined controlled vocabularies of consumables, equipment, protocols and software help describe each step of the cryoEM workflow in a structured manner. gP2S is widely configurable and, depending on the team's needs, may exist as a standalone product or be a part of a broader ecosystem of scientific applications, integrating via REST APIs with project management tools, applications tracking the production of proteins or of small molecules ligands, or applications automating data collection and storage. Users can register details of each grid and microscopy session including key experimental metadata and parameter values, and the lineage of each experimental artifact (sample, grid, microscopy session, map, etc.) is recorded. gP2S serves as a cryoEM experimental workflow organizer that enables accurate record keeping for teams, and is available under an open-source license.
    Keywords Internet ; computer software ; crystallography ; data collection ; ecosystems ; electron microscopy ; equipment ; information management ; ligands ; management systems ; metadata ; models ; teams
    Language English
    Dates of publication 2021-0610
    Size p. e62377.
    Publishing place Journal of Visualized Experiments
    Document type Article
    Note NAL-AP-2-clean
    ZDB-ID 2259946-0
    ISSN 1940-087X
    ISSN 1940-087X
    DOI 10.3791/62377
    Database NAL-Catalogue (AGRICOLA)

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  4. Article ; Online: Tripartite DNA Lesion Recognition and Verification by XPC, TFIIH, and XPA in Nucleotide Excision Repair.

    Li, Chia-Lung / Golebiowski, Filip M / Onishi, Yuki / Samara, Nadine L / Sugasawa, Kaoru / Yang, Wei

    Molecular cell

    2015  Volume 59, Issue 6, Page(s) 1025–1034

    Abstract: Transcription factor IIH (TFIIH) is essential for both transcription and nucleotide excision repair (NER). DNA lesions are initially detected by NER factors XPC and XPE or stalled RNA polymerases, but only bulky lesions are preferentially repaired by NER. ...

    Abstract Transcription factor IIH (TFIIH) is essential for both transcription and nucleotide excision repair (NER). DNA lesions are initially detected by NER factors XPC and XPE or stalled RNA polymerases, but only bulky lesions are preferentially repaired by NER. To elucidate substrate specificity in NER, we have prepared homogeneous human ten-subunit TFIIH and its seven-subunit core (Core7) without the CAK module and show that bulky lesions in DNA inhibit the ATPase and helicase activities of both XPB and XPD in Core7 to promote NER, whereas non-genuine NER substrates have no such effect. Moreover, the NER factor XPA activates unwinding of normal DNA by Core7, but inhibits the Core7 helicase activity in the presence of bulky lesions. Finally, the CAK module inhibits DNA binding by TFIIH and thereby enhances XPC-dependent specific recruitment of TFIIH. Our results support a tripartite lesion verification mechanism involving XPC, TFIIH, and XPA for efficient NER.
    MeSH term(s) Animals ; Cisplatin/chemistry ; DNA Adducts/chemistry ; DNA Adducts/genetics ; DNA Repair ; DNA, Single-Stranded/physiology ; DNA-Binding Proteins/chemistry ; DNA-Binding Proteins/physiology ; Electrophoretic Mobility Shift Assay ; Humans ; Protein Binding ; Sf9 Cells ; Spodoptera ; Transcription Factor TFIIH/chemistry ; Transcription Factor TFIIH/physiology ; Xeroderma Pigmentosum Group A Protein/chemistry ; Xeroderma Pigmentosum Group A Protein/physiology
    Chemical Substances DNA Adducts ; DNA, Single-Stranded ; DNA-Binding Proteins ; XPA protein, human ; Xeroderma Pigmentosum Group A Protein ; Transcription Factor TFIIH (148710-81-0) ; XPC protein, human (156533-34-5) ; Cisplatin (Q20Q21Q62J)
    Language English
    Publishing date 2015-07-08
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 1415236-8
    ISSN 1097-4164 ; 1097-2765
    ISSN (online) 1097-4164
    ISSN 1097-2765
    DOI 10.1016/j.molcel.2015.08.012
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Efficient overexpression and purification of active full-length human transcription factor Yin Yang 1 in Escherichia coli.

    Golebiowski, Filip M / Górecki, Andrzej / Bonarek, Piotr / Dziedzicka-Wasylewska, Marta

    Protein expression and purification

    2011  Volume 77, Issue 2, Page(s) 198–206

    Abstract: The Yin Yang 1 protein is a zinc finger transcription factor involved in the regulation of diverse cellular processes through DNA and protein-protein interactions. Here we present an improved method for the expression and purification of the human full- ... ...

    Abstract The Yin Yang 1 protein is a zinc finger transcription factor involved in the regulation of diverse cellular processes through DNA and protein-protein interactions. Here we present an improved method for the expression and purification of the human full-length YY1 protein from Escherichia coli. The protein was first purified using denaturing conditions, refolded using optimized conditions and then purified using a DNA-affinity column to ≥ 95% purity; this process provided a high final yield and highly active protein. The protein was active in EMSA and the fluorescence anisotropy assays. The protein retained its full activity and its initial concentration for several months when stored at -80° C. Thus, we have obtained YY1 protein with levels of activity and concentration that are suitable for spectroscopic and other biochemical studies.
    MeSH term(s) Binding Sites ; Chromatography, Affinity ; Cloning, Molecular ; DNA/metabolism ; Electrophoretic Mobility Shift Assay ; Escherichia coli ; Fluorescence Polarization ; Gene Expression ; Histidine/metabolism ; Humans ; Inclusion Bodies/genetics ; Inclusion Bodies/metabolism ; Oligopeptides/metabolism ; Plasmids/genetics ; Plasmids/metabolism ; Protein Binding ; Protein Denaturation ; Protein Engineering/methods ; Protein Refolding ; Protein Stability ; Recombinant Proteins/genetics ; Recombinant Proteins/isolation & purification ; Recombinant Proteins/metabolism ; YY1 Transcription Factor/genetics ; YY1 Transcription Factor/isolation & purification ; YY1 Transcription Factor/metabolism ; Zinc Fingers
    Chemical Substances His-His-His-His-His-His ; Oligopeptides ; Recombinant Proteins ; YY1 Transcription Factor ; YY1 protein, human ; Histidine (4QD397987E) ; DNA (9007-49-2)
    Language English
    Publishing date 2011-06
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1055455-5
    ISSN 1096-0279 ; 1046-5928
    ISSN (online) 1096-0279
    ISSN 1046-5928
    DOI 10.1016/j.pep.2011.01.016
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: An engineered IL-2 partial agonist promotes CD8

    Mo, Fei / Yu, Zhiya / Li, Peng / Oh, Jangsuk / Spolski, Rosanne / Zhao, Liang / Glassman, Caleb R / Yamamoto, Tori N / Chen, Yun / Golebiowski, Filip M / Hermans, Dalton / Majri-Morrison, Sonia / Picton, Lora K / Liao, Wei / Ren, Min / Zhuang, Xiaoxuan / Mitra, Suman / Lin, Jian-Xin / Gattinoni, Luca /
    Powell, Jonathan D / Restifo, Nicholas P / Garcia, K Christopher / Leonard, Warren J

    Nature

    2021  Volume 597, Issue 7877, Page(s) 544–548

    Abstract: Adoptive transfer of antigen-specific T cells represents a major advance in cancer immunotherapy, with robust clinical outcomes in some ... ...

    Abstract Adoptive transfer of antigen-specific T cells represents a major advance in cancer immunotherapy, with robust clinical outcomes in some patients
    MeSH term(s) Animals ; CD8-Positive T-Lymphocytes/cytology ; CD8-Positive T-Lymphocytes/drug effects ; CD8-Positive T-Lymphocytes/immunology ; Cell Differentiation/drug effects ; Drug Partial Agonism ; Interleukin-2/agonists ; Interleukin-2/analogs & derivatives ; Interleukin-2/chemistry ; Interleukin-2/genetics ; Melanoma/metabolism ; Mice ; Mitochondria/drug effects ; Mutant Proteins/chemistry ; Mutant Proteins/genetics ; Mutant Proteins/pharmacology ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/metabolism ; Receptors, Antigen, T-Cell/genetics ; Receptors, Antigen, T-Cell/metabolism ; STAT5 Transcription Factor/metabolism ; Stem Cells/cytology ; Stem Cells/drug effects ; T Cell Transcription Factor 1/metabolism ; Translational Research, Biomedical
    Chemical Substances Interleukin-2 ; Mutant Proteins ; Receptors, Antigen, T-Cell ; STAT5 Transcription Factor ; T Cell Transcription Factor 1 ; TCF7 protein, human
    Language English
    Publishing date 2021-09-15
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 120714-3
    ISSN 1476-4687 ; 0028-0836
    ISSN (online) 1476-4687
    ISSN 0028-0836
    DOI 10.1038/s41586-021-03861-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Efficient overexpression and purification of active full-length human transcription factor Yin Yang 1 in Escherichia coli

    Golebiowski, Filip M / Górecki, Andrzej / Bonarek, Piotr / Dziedzicka-Wasylewska, Marta

    Protein expression and purification. 2011 June, v. 77, no. 2

    2011  

    Abstract: The Yin Yang 1 protein is a zinc finger transcription factor involved in the regulation of diverse cellular processes through DNA and protein–protein interactions. Here we present an improved method for the expression and purification of the human full- ... ...

    Abstract The Yin Yang 1 protein is a zinc finger transcription factor involved in the regulation of diverse cellular processes through DNA and protein–protein interactions. Here we present an improved method for the expression and purification of the human full-length YY1 protein from Escherichia coli. The protein was first purified using denaturing conditions, refolded using optimized conditions and then purified using a DNA-affinity column to ⩾95% purity; this process provided a high final yield and highly active protein. The protein was active in EMSA and the fluorescence anisotropy assays. The protein retained its full activity and its initial concentration for several months when stored at −80°C. Thus, we have obtained YY1 protein with levels of activity and concentration that are suitable for spectroscopic and other biochemical studies.
    Keywords DNA ; Escherichia coli ; fluorescence ; gene overexpression ; humans ; protein-protein interactions ; spectroscopy ; transcription factors ; zinc finger motif
    Language English
    Dates of publication 2011-06
    Size p. 198-206.
    Publishing place Elsevier Inc.
    Document type Article
    ZDB-ID 1055455-5
    ISSN 1096-0279 ; 1046-5928
    ISSN (online) 1096-0279
    ISSN 1046-5928
    DOI 10.1016/j.pep.2011.01.016
    Database NAL-Catalogue (AGRICOLA)

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  8. Article ; Online: An investigation of the affinities, specificity and kinetics involved in the interaction between the Yin Yang 1 transcription factor and DNA.

    Golebiowski, Filip M / Górecki, Andrzej / Bonarek, Piotr / Rapala-Kozik, Maria / Kozik, Andrzej / Dziedzicka-Wasylewska, Marta

    The FEBS journal

    2012  Volume 279, Issue 17, Page(s) 3147–3158

    Abstract: Human transcription factor Yin Yang 1 (YY1) is a four zinc-finger protein that regulates a large number of genes with various biological functions in processes such as development, carcinogenesis and B-cell maturation. The natural binding sites of YY1 ... ...

    Abstract Human transcription factor Yin Yang 1 (YY1) is a four zinc-finger protein that regulates a large number of genes with various biological functions in processes such as development, carcinogenesis and B-cell maturation. The natural binding sites of YY1 are relatively unconserved and have a short core sequence (CCAT). We were interested in determining how YY1 recognizes its binding sites and achieves the necessary sequence selectivity in the cell. Using fluorescence anisotropy, we determined the equilibrium dissociation constants for selected naturally occurring YY1 binding sites that have various levels of similarity to the consensus sequence. We found that recombinant YY1 interacts with its specific binding sites with relatively low affinities from the high nanomolar to the low micromolar range. Using a fluorescence anisotropy competition assay, we determined the affinity of YY1 for non-specific DNA to be between 30 and 40 μm, which results in low specificity ratios of between 3 and 220. Additionally, surface plasmon resonance measurements showed rapid association and dissociation rates, suggesting that the binding strength is regulated through changes in both k(a) and k(d). In conclusion, we propose that, in the cell, YY1 may achieve higher specificity by associating with co-regulators or as a part of multi-subunit complexes.
    MeSH term(s) Base Sequence ; DNA/metabolism ; DNA Primers ; Fluorescence Polarization ; Humans ; Kinetics ; Protein Binding ; Surface Plasmon Resonance ; YY1 Transcription Factor/metabolism
    Chemical Substances DNA Primers ; YY1 Transcription Factor ; YY1 protein, human ; DNA (9007-49-2)
    Language English
    Publishing date 2012-09
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2173655-8
    ISSN 1742-4658 ; 1742-464X
    ISSN (online) 1742-4658
    ISSN 1742-464X
    DOI 10.1111/j.1742-4658.2012.08693.x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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