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  1. Article ; Online: Structural Dynamics Predominantly Determine the Adaptability of Proteins to Amino Acid Deletions.

    Banerjee, Anupam / Bahar, Ivet

    International journal of molecular sciences

    2023  Volume 24, Issue 9

    Abstract: The insertion or deletion (indel) of amino acids has a variety of effects on protein function, ranging from disease-forming changes to gaining new functions. Despite their importance, indels have not been systematically characterized towards protein ... ...

    Abstract The insertion or deletion (indel) of amino acids has a variety of effects on protein function, ranging from disease-forming changes to gaining new functions. Despite their importance, indels have not been systematically characterized towards protein engineering or modification goals. In the present work, we focus on deletions composed of multiple contiguous amino acids (mAA-dels) and their effects on the protein (mutant) folding ability. Our analysis reveals that the mutant retains the native fold when the mAA-del obeys well-defined structural dynamics properties: localization in intrinsically flexible regions, showing low resistance to mechanical stress, and separation from allosteric signaling paths. Motivated by the possibility of distinguishing the features that underlie the adaptability of proteins to mAA-dels, and by the rapid evaluation of these features using elastic network models, we developed a positive-unlabeled learning-based classifier that can be adopted for protein design purposes. Trained on a consolidated set of features, including those reflecting the intrinsic dynamics of the regions where the mAA-dels occur, the new classifier yields a high recall of 84.3% for identifying mAA-dels that are stably tolerated by the protein. The comparative examination of the relative contribution of different features to the prediction reveals the dominant role of structural dynamics in enabling the adaptation of the mutant to mAA-del without disrupting the native fold.
    MeSH term(s) Amino Acids/genetics ; Proteins/chemistry ; INDEL Mutation ; Protein Engineering
    Chemical Substances Amino Acids ; Proteins
    Language English
    Publishing date 2023-05-08
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms24098450
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Genome structural dynamics: insights from Gaussian network analysis of Hi-C data.

    Banerjee, Anupam / Zhang, She / Bahar, Ivet

    Briefings in functional genomics

    2024  

    Abstract: Characterization of the spatiotemporal properties of the chromatin is essential to gaining insights into the physical bases of gene co-expression, transcriptional regulation and epigenetic modifications. The Gaussian network model (GNM) has proven in ... ...

    Abstract Characterization of the spatiotemporal properties of the chromatin is essential to gaining insights into the physical bases of gene co-expression, transcriptional regulation and epigenetic modifications. The Gaussian network model (GNM) has proven in recent work to serve as a useful tool for modeling chromatin structural dynamics, using as input high-throughput chromosome conformation capture data. We focus here on the exploration of the collective dynamics of chromosomal structures at hierarchical levels of resolution, from single gene loci to topologically associating domains or entire chromosomes. The GNM permits us to identify long-range interactions between gene loci, shedding light on the role of cross-correlations between distal regions of the chromosomes in regulating gene expression. Notably, GNM analysis performed across diverse cell lines highlights the conservation of the global/cooperative movements of the chromatin across different types of cells. Variations driven by localized couplings between genomic loci, on the other hand, underlie cell differentiation, underscoring the significance of the four-dimensional properties of the genome in defining cellular identity. Finally, we demonstrate the close relation between the cell type-dependent mobility profiles of gene loci and their gene expression patterns, providing a clear demonstration of the role of chromosomal 4D features in defining cell-specific differential expression of genes.
    Language English
    Publishing date 2024-04-22
    Publishing country England
    Document type Journal Article
    ZDB-ID 2540916-5
    ISSN 2041-2657 ; 2041-2649 ; 2041-2647
    ISSN (online) 2041-2657
    ISSN 2041-2649 ; 2041-2647
    DOI 10.1093/bfgp/elae014
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Book ; Online: Faculty Opinions recommendation of Structural basis for the recognition of SARS-CoV-2 by full-length human ACE2.

    Bahar, Ivet

    Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature

    2020  

    Keywords covid19
    Publisher Faculty Opinions Ltd
    Publishing country uk
    Document type Book ; Online
    DOI 10.3410/f.737476161.793576265
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  4. Article: Structural mechanisms for VMAT2 inhibition by tetrabenazine.

    Dalton, Michael P / Cheng, Mary Hongying / Bahar, Ivet / Coleman, Jonathan A

    bioRxiv : the preprint server for biology

    2024  

    Abstract: The vesicular monoamine transporter 2 (VMAT2) is a proton-dependent antiporter responsible for loading monoamine neurotransmitters into synaptic vesicles. Dysregulation of VMAT2 can lead to several neuropsychiatric disorders including Parkinson's disease ...

    Abstract The vesicular monoamine transporter 2 (VMAT2) is a proton-dependent antiporter responsible for loading monoamine neurotransmitters into synaptic vesicles. Dysregulation of VMAT2 can lead to several neuropsychiatric disorders including Parkinson's disease and schizophrenia. Furthermore, drugs such as amphetamine and MDMA are known to act on VMAT2, exemplifying its role in the mechanisms of actions for drugs of abuse. Despite VMAT2's importance, there remains a critical lack of mechanistic understanding, largely driven by a lack of structural information. Here we report a 3.1 Å resolution cryo-EM structure of VMAT2 complexed with tetrabenazine (TBZ), a non-competitive inhibitor used in the treatment of Huntington's chorea. We find TBZ interacts with residues in a central binding site, locking VMAT2 in an occluded conformation and providing a mechanistic basis for non-competitive inhibition. We further identify residues critical for cytosolic and lumenal gating, including a cluster of hydrophobic residues which are involved in a lumenal gating strategy. Our structure also highlights three distinct polar networks that may determine VMAT2 conformational dynamics and play a role in proton transduction. The structure elucidates mechanisms of VMAT2 inhibition and transport, providing insights into VMAT2 architecture, function, and the design of small-molecule therapeutics.
    Language English
    Publishing date 2024-02-01
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2023.09.05.556211
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Structural mechanisms for VMAT2 inhibition by tetrabenazine.

    Dalton, Michael P / Cheng, Mary Hongying / Bahar, Ivet / Coleman, Jonathan A

    eLife

    2024  Volume 12

    Abstract: The vesicular monoamine transporter 2 (VMAT2) is a proton-dependent antiporter responsible for loading monoamine neurotransmitters into synaptic vesicles. Dysregulation of VMAT2 can lead to several neuropsychiatric disorders including Parkinson's disease ...

    Abstract The vesicular monoamine transporter 2 (VMAT2) is a proton-dependent antiporter responsible for loading monoamine neurotransmitters into synaptic vesicles. Dysregulation of VMAT2 can lead to several neuropsychiatric disorders including Parkinson's disease and schizophrenia. Furthermore, drugs such as amphetamine and MDMA are known to act on VMAT2, exemplifying its role in the mechanisms of actions for drugs of abuse. Despite VMAT2's importance, there remains a critical lack of mechanistic understanding, largely driven by a lack of structural information. Here, we report a 3.1 Å resolution cryo-electron microscopy (cryo-EM) structure of VMAT2 complexed with tetrabenazine (TBZ), a non-competitive inhibitor used in the treatment of Huntington's chorea. We find TBZ interacts with residues in a central binding site, locking VMAT2 in an occluded conformation and providing a mechanistic basis for non-competitive inhibition. We further identify residues critical for cytosolic and lumenal gating, including a cluster of hydrophobic residues which are involved in a lumenal gating strategy. Our structure also highlights three distinct polar networks that may determine VMAT2 conformational dynamics and play a role in proton transduction. The structure elucidates mechanisms of VMAT2 inhibition and transport, providing insights into VMAT2 architecture, function, and the design of small-molecule therapeutics.
    MeSH term(s) Humans ; Tetrabenazine/metabolism ; Tetrabenazine/pharmacology ; Vesicular Monoamine Transport Proteins/chemistry ; Vesicular Monoamine Transport Proteins/metabolism ; Protons ; Cryoelectron Microscopy ; Huntington Disease
    Chemical Substances Tetrabenazine (Z9O08YRN8O) ; Vesicular Monoamine Transport Proteins ; Protons
    Language English
    Publishing date 2024-03-22
    Publishing country England
    Document type Journal Article
    ZDB-ID 2687154-3
    ISSN 2050-084X ; 2050-084X
    ISSN (online) 2050-084X
    ISSN 2050-084X
    DOI 10.7554/eLife.91973
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Allo-targeting of the kinase domain: Insights from in silico studies and comparison with experiments.

    Lee, Ji Young / Gebauer, Emma / Seeliger, Markus A / Bahar, Ivet

    Current opinion in structural biology

    2024  Volume 84, Page(s) 102770

    Abstract: The eukaryotic protein kinase domain has been a broadly explored target for drug discovery, despite limitations imposed by its high sequence conservation as a shared modular domain and the development of resistance to drugs. One way of addressing those ... ...

    Abstract The eukaryotic protein kinase domain has been a broadly explored target for drug discovery, despite limitations imposed by its high sequence conservation as a shared modular domain and the development of resistance to drugs. One way of addressing those limitations has been to target its potential allosteric sites, shortly called allo-targeting, in conjunction with, or separately from, its conserved catalytic/orthosteric site that has been widely exploited. Allosteric regulation has gained importance as an alternative to overcome the drawbacks associated with the indiscriminate effect of targeting the active site, and it turned out to be particularly useful for these highly promiscuous and broadly shared kinase domains. Yet, allo-targeting often faces challenges as the allosteric sites are not as clearly defined as its orthosteric sites, and the effect on the protein function may not be unambiguously assessed. A robust understanding of the consequence of site-specific allo-targeting on the conformational dynamics of the target protein is essential to design effective allo-targeting strategies. Recent years have seen important advances in in silico identification of druggable sites and distinguishing among them those sites expected to allosterically mediate conformational switches essential to signal transmission. The present opinion underscores the utility of such computational approaches applied to the kinase domain, with the help of comparison between computational predictions and experimental observations.
    MeSH term(s) Allosteric Site ; Allosteric Regulation ; Proteins/chemistry ; Drug Discovery ; Catalytic Domain
    Chemical Substances Proteins
    Language English
    Publishing date 2024-01-11
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 1068353-7
    ISSN 1879-033X ; 0959-440X
    ISSN (online) 1879-033X
    ISSN 0959-440X
    DOI 10.1016/j.sbi.2023.102770
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Harold A. Scheraga (10/18/1921-8/1/2020): A pioneering scientist who laid the foundations of protein science in the 20th century.

    Meirovitch, Hagai / Bahar, Ivet

    Proceedings of the National Academy of Sciences of the United States of America

    2021  Volume 118, Issue 8

    MeSH term(s) Biophysics/history ; History, 20th Century ; History, 21st Century ; Humans ; Proteins/history ; Science/history ; United States
    Chemical Substances Proteins
    Language English
    Publishing date 2021-02-25
    Publishing country United States
    Document type Biography ; Historical Article ; Journal Article
    ZDB-ID 209104-5
    ISSN 1091-6490 ; 0027-8424
    ISSN (online) 1091-6490
    ISSN 0027-8424
    DOI 10.1073/pnas.2026796118
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: Editorial: Targeting Membrane Proteins: Structure-Function-Dynamics Relationships.

    Colas, Claire / Bahar, Ivet / Shi, Lei / Font Sadurni, Josep

    Frontiers in chemistry

    2022  Volume 10, Page(s) 862802

    Language English
    Publishing date 2022-03-03
    Publishing country Switzerland
    Document type Editorial
    ZDB-ID 2711776-5
    ISSN 2296-2646
    ISSN 2296-2646
    DOI 10.3389/fchem.2022.862802
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Multisystem Inflammatory Syndrome in Children in the United States.

    Arditi, Moshe / Bahar, Ivet

    The New England journal of medicine

    2020  Volume 383, Issue 18, Page(s) 1794

    MeSH term(s) COVID-19 ; Child ; Coronavirus Infections/epidemiology ; Humans ; Pandemics ; Pneumonia, Viral/epidemiology ; Syndrome ; Systemic Inflammatory Response Syndrome ; United States/epidemiology
    Keywords covid19
    Language English
    Publishing date 2020-10-21
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 207154-x
    ISSN 1533-4406 ; 0028-4793
    ISSN (online) 1533-4406
    ISSN 0028-4793
    DOI 10.1056/NEJMc2026136
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Editorial

    Claire Colas / Ivet Bahar / Lei Shi / Josep Font Sadurni

    Frontiers in Chemistry, Vol

    Targeting Membrane Proteins: Structure-Function-Dynamics Relationships

    2022  Volume 10

    Keywords membrane proteins ; drug targets ; structure ; function ; dynamics ; Chemistry ; QD1-999
    Language English
    Publishing date 2022-03-01T00:00:00Z
    Publisher Frontiers Media S.A.
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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