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  1. AU="Tysinger, Emma"
  2. AU=Covarrubias David
  3. AU="Dino Papeš"
  4. AU="Assis, Daniel Barbosa"
  5. AU="Lauquin, Guy J-M"

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  1. Article ; Online: Can We Quickly Learn to "Translate" Bioactive Molecules with Transformer Models?

    Tysinger, Emma P / Rai, Brajesh K / Sinitskiy, Anton V

    Journal of chemical information and modeling

    2023  Volume 63, Issue 6, Page(s) 1734–1744

    Abstract: Meaningful exploration of the chemical space of druglike molecules in drug design is a highly challenging task due to a combinatorial explosion of possible modifications of molecules. In this work, we address this problem with transformer models, a type ... ...

    Abstract Meaningful exploration of the chemical space of druglike molecules in drug design is a highly challenging task due to a combinatorial explosion of possible modifications of molecules. In this work, we address this problem with transformer models, a type of machine learning (ML) model originally developed for machine translation. By training transformer models on pairs of similar bioactive molecules from the public ChEMBL data set, we enable them to learn medicinal-chemistry-meaningful, context-dependent transformations of molecules, including those absent from the training set. By retrospective analysis on the performance of transformer models on ChEMBL subsets of ligands binding to COX2, DRD2, or HERG protein targets, we demonstrate that the models can generate structures identical or highly similar to most active ligands, despite the models having not seen any ligands active against the corresponding protein target during training. Our work demonstrates that human experts working on hit expansion in drug design can easily and quickly employ transformer models, originally developed to translate texts from one natural language to another, to "translate" from known molecules active against a given protein target to novel molecules active against the same target.
    MeSH term(s) Humans ; Retrospective Studies ; Machine Learning ; Drug Design
    Language English
    Publishing date 2023-03-13
    Publishing country United States
    Document type Journal Article
    ZDB-ID 190019-5
    ISSN 1549-960X ; 0095-2338
    ISSN (online) 1549-960X
    ISSN 0095-2338
    DOI 10.1021/acs.jcim.2c01618
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: PAM-Flexible Genome Editing with an Engineered Chimeric Cas9.

    Koseki, Sabrina / Hong, Lauren / Yudistyra, Vivian / Stan, Teodora / Tysinger, Emma / Silverstein, Rachel / Kramme, Christian / Amrani, Nadia / Savic, Natasha / Pacesa, Martin / Rodriguez, Tomás / Ponnapati, Manvitha / Jacobson, Joseph / Church, George / Truant, Ray / Jinek, Martin / Kleinstiver, Benjamin / Sontheimer, Erik / Chatterjee, Pranam

    Research square

    2023  

    Abstract: CRISPR enzymes require a defined protospacer adjacent motif (PAM) flanking a guide RNA-programmed target site, limiting their sequence accessibility for robust genome editing applications. In this study, we recombine the PAM-interacting domain of SpRY, a ...

    Abstract CRISPR enzymes require a defined protospacer adjacent motif (PAM) flanking a guide RNA-programmed target site, limiting their sequence accessibility for robust genome editing applications. In this study, we recombine the PAM-interacting domain of SpRY, a broad-targeting Cas9 possessing an NRN > NYN PAM preference, with the N-terminus of Sc++, a Cas9 with simultaneously broad, efficient, and accurate NNG editing capabilities, to generate a chimeric enzyme with highly flexible PAM preference: SpRYc. We demonstrate that SpRYc leverages properties of both enzymes to specifically edit diverse NNN PAMs and disease-related loci for potential therapeutic applications. In total, the unique approaches to generate SpRYc, coupled with its robust flexibility, highlight the power of integrative protein design for Cas9 engineering and motivate downstream editing applications that require precise genomic positioning.
    Language English
    Publishing date 2023-03-07
    Publishing country United States
    Document type Preprint
    DOI 10.21203/rs.3.rs-2625838/v1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Correction: Directed differentiation of human iPSCs to functional ovarian granulosa-like cells via transcription factor overexpression.

    Pierson Smela, Merrick D / Kramme, Christian C / Fortuna, Patrick R J / Adams, Jessica L / Su, Alina Rui / Dong, Edward / Kobayashi, Mutsumi / Brixi, Garyk / Kavirayuni, Venkata Srikar / Tysinger, Emma / Kohman, Richie E / Shioda, Toshi / Chatterjee, Pranam / Church, George M

    eLife

    2023  Volume 12

    Language English
    Publishing date 2023-03-22
    Publishing country England
    Document type Published Erratum
    ZDB-ID 2687154-3
    ISSN 2050-084X ; 2050-084X
    ISSN (online) 2050-084X
    ISSN 2050-084X
    DOI 10.7554/eLife.87987
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Directed differentiation of human iPSCs to functional ovarian granulosa-like cells via transcription factor overexpression.

    Pierson Smela, Merrick D / Kramme, Christian C / Fortuna, Patrick R J / Adams, Jessica L / Su, Rui / Dong, Edward / Kobayashi, Mutsumi / Brixi, Garyk / Kavirayuni, Venkata Srikar / Tysinger, Emma / Kohman, Richie E / Shioda, Toshi / Chatterjee, Pranam / Church, George M

    eLife

    2023  Volume 12

    Abstract: An in vitro model of human ovarian follicles would greatly benefit the study of female reproduction. Ovarian development requires the combination of germ cells and several types of somatic cells. Among these, granulosa cells play a key role in follicle ... ...

    Abstract An in vitro model of human ovarian follicles would greatly benefit the study of female reproduction. Ovarian development requires the combination of germ cells and several types of somatic cells. Among these, granulosa cells play a key role in follicle formation and support for oogenesis. Whereas efficient protocols exist for generating human primordial germ cell-like cells (hPGCLCs) from human induced pluripotent stem cells (hiPSCs), a method of generating granulosa cells has been elusive. Here, we report that simultaneous overexpression of two transcription factors (TFs) can direct the differentiation of hiPSCs to granulosa-like cells. We elucidate the regulatory effects of several granulosa-related TFs and establish that overexpression of NR5A1 and either RUNX1 or RUNX2 is sufficient to generate granulosa-like cells. Our granulosa-like cells have transcriptomes similar to human fetal ovarian cells and recapitulate key ovarian phenotypes including follicle formation and steroidogenesis. When aggregated with hPGCLCs, our cells form ovary-like organoids (ovaroids) and support hPGCLC development from the premigratory to the gonadal stage as measured by induction of DAZL expression. This model system will provide unique opportunities for studying human ovarian biology and may enable the development of therapies for female reproductive health.
    MeSH term(s) Humans ; Female ; Transcription Factors/metabolism ; Induced Pluripotent Stem Cells ; Ovary/metabolism ; Oogenesis ; Cell Differentiation
    Chemical Substances Transcription Factors
    Language English
    Publishing date 2023-02-21
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2687154-3
    ISSN 2050-084X ; 2050-084X
    ISSN (online) 2050-084X
    ISSN 2050-084X
    DOI 10.7554/eLife.83291
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: A Cas9 with PAM recognition for adenine dinucleotides.

    Chatterjee, Pranam / Lee, Jooyoung / Nip, Lisa / Koseki, Sabrina R T / Tysinger, Emma / Sontheimer, Erik J / Jacobson, Joseph M / Jakimo, Noah

    Nature communications

    2020  Volume 11, Issue 1, Page(s) 2474

    Abstract: CRISPR-associated (Cas) DNA-endonucleases are remarkably effective tools for genome engineering, but have limited target ranges due to their protospacer adjacent motif (PAM) requirements. We demonstrate a critical expansion of the targetable sequence ... ...

    Abstract CRISPR-associated (Cas) DNA-endonucleases are remarkably effective tools for genome engineering, but have limited target ranges due to their protospacer adjacent motif (PAM) requirements. We demonstrate a critical expansion of the targetable sequence space for a type II-A CRISPR-associated enzyme through identification of the natural 5[Formula: see text]-NAAN-3[Formula: see text] PAM preference of Streptococcus macacae Cas9 (SmacCas9). To achieve efficient editing activity, we graft the PAM-interacting domain of SmacCas9 to its well-established ortholog from Streptococcus pyogenes (SpyCas9), and further engineer an increased efficiency variant (iSpyMac) for robust genome editing activity. We establish that our hybrids can target all adenine dinucleotide PAM sequences and possess robust and accurate editing capabilities in human cells.
    MeSH term(s) Adenine/metabolism ; Amino Acid Sequence ; CRISPR-Associated Protein 9/chemistry ; CRISPR-Associated Protein 9/metabolism ; Dinucleoside Phosphates/metabolism ; Gene Editing ; HEK293 Cells ; Humans ; Nucleotide Motifs/genetics ; Reproducibility of Results ; Streptococcus/genetics
    Chemical Substances Dinucleoside Phosphates ; CRISPR-Associated Protein 9 (EC 3.1.-) ; Adenine (JAC85A2161)
    Language English
    Publishing date 2020-05-18
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-020-16117-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: PAM-flexible genome editing with an engineered chimeric Cas9.

    Zhao, Lin / Koseki, Sabrina R T / Silverstein, Rachel A / Amrani, Nadia / Peng, Christina / Kramme, Christian / Savic, Natasha / Pacesa, Martin / Rodríguez, Tomás C / Stan, Teodora / Tysinger, Emma / Hong, Lauren / Yudistyra, Vivian / Ponnapati, Manvitha R / Jacobson, Joseph M / Church, George M / Jakimo, Noah / Truant, Ray / Jinek, Martin /
    Kleinstiver, Benjamin P / Sontheimer, Erik J / Chatterjee, Pranam

    Nature communications

    2023  Volume 14, Issue 1, Page(s) 6175

    Abstract: CRISPR enzymes require a defined protospacer adjacent motif (PAM) flanking a guide RNA-programmed target site, limiting their sequence accessibility for robust genome editing applications. In this study, we recombine the PAM-interacting domain of SpRY, a ...

    Abstract CRISPR enzymes require a defined protospacer adjacent motif (PAM) flanking a guide RNA-programmed target site, limiting their sequence accessibility for robust genome editing applications. In this study, we recombine the PAM-interacting domain of SpRY, a broad-targeting Cas9 possessing an NRN > NYN (R = A or G, Y = C or T) PAM preference, with the N-terminus of Sc + +, a Cas9 with simultaneously broad, efficient, and accurate NNG editing capabilities, to generate a chimeric enzyme with highly flexible PAM preference: SpRYc. We demonstrate that SpRYc leverages properties of both enzymes to specifically edit diverse PAMs and disease-related loci for potential therapeutic applications. In total, the approaches to generate SpRYc, coupled with its robust flexibility, highlight the power of integrative protein design for Cas9 engineering and motivate downstream editing applications that require precise genomic positioning.
    MeSH term(s) Gene Editing ; CRISPR-Cas Systems/genetics ; CRISPR-Associated Protein 9/genetics ; CRISPR-Associated Protein 9/metabolism ; Genome
    Chemical Substances CRISPR-Associated Protein 9 (EC 3.1.-)
    Language English
    Publishing date 2023-10-04
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2553671-0
    ISSN 2041-1723 ; 2041-1723
    ISSN (online) 2041-1723
    ISSN 2041-1723
    DOI 10.1038/s41467-023-41829-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: An engineered ScCas9 with broad PAM range and high specificity and activity.

    Chatterjee, Pranam / Jakimo, Noah / Lee, Jooyoung / Amrani, Nadia / Rodríguez, Tomás / Koseki, Sabrina R T / Tysinger, Emma / Qing, Rui / Hao, Shilei / Sontheimer, Erik J / Jacobson, Joseph

    Nature biotechnology

    2020  Volume 38, Issue 10, Page(s) 1154–1158

    Abstract: CRISPR enzymes require a protospacer-adjacent motif (PAM) near the target cleavage site, constraining the sequences accessible for editing. In the present study, we combine protein motifs from several orthologs to engineer two variants of Streptococcus ... ...

    Abstract CRISPR enzymes require a protospacer-adjacent motif (PAM) near the target cleavage site, constraining the sequences accessible for editing. In the present study, we combine protein motifs from several orthologs to engineer two variants of Streptococcus canis Cas9-Sc
    MeSH term(s) Amino Acid Motifs/genetics ; CRISPR-Associated Protein 9/genetics ; CRISPR-Cas Systems/genetics ; Clustered Regularly Interspaced Short Palindromic Repeats/genetics ; DNA Cleavage ; Gene Editing/methods ; Streptococcus/genetics
    Chemical Substances CRISPR-Associated Protein 9 (EC 3.1.-)
    Language English
    Publishing date 2020-05-11
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 1311932-1
    ISSN 1546-1696 ; 1087-0156
    ISSN (online) 1546-1696
    ISSN 1087-0156
    DOI 10.1038/s41587-020-0517-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Publisher Correction: An engineered ScCas9 with broad PAM range and high specificity and activity.

    Chatterjee, Pranam / Jakimo, Noah / Lee, Jooyoung / Amrani, Nadia / Rodríguez, Tomás / Koseki, Sabrina R T / Tysinger, Emma / Qing, Rui / Hao, Shilei / Sontheimer, Erik J / Jacobson, Joseph

    Nature biotechnology

    2020  Volume 38, Issue 10, Page(s) 1212

    Abstract: An amendment to this paper has been published and can be accessed via a link at the top of the paper. ...

    Abstract An amendment to this paper has been published and can be accessed via a link at the top of the paper.
    Language English
    Publishing date 2020-01-25
    Publishing country United States
    Document type Published Erratum
    ZDB-ID 1311932-1
    ISSN 1546-1696 ; 1087-0156
    ISSN (online) 1546-1696
    ISSN 1087-0156
    DOI 10.1038/s41587-020-0604-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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