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  1. Artikel: Atomistic level characterisation of ssDNA translocation through the E. coli proteins CsgG and CsgF for nanopore sequencing

    Rattu, Punam / Glencross, Flo / Mader, Sophie L. / Skylaris, Chris-Kriton / Matthews, Stephen J. / Rouse, Sarah L. / Khalid, Syma

    Computational and Structural Biotechnology Journal. 2021, v. 19

    2021  

    Abstract: Two proteins of the Escherichia coli membrane protein complex, CsgG and CsgF, are studied as proteinaceous nanopores for DNA sequencing. It is highly desirable to control the DNA as it moves through the pores, this requires characterisation of DNA ... ...

    Abstract Two proteins of the Escherichia coli membrane protein complex, CsgG and CsgF, are studied as proteinaceous nanopores for DNA sequencing. It is highly desirable to control the DNA as it moves through the pores, this requires characterisation of DNA translocation and subsequent optimization of the pores. In order to inform protein engineering to improve the pores, we have conducted a series of molecular dynamics simulations to characterise the mechanical strength and conformational dynamics of CsgG and the CsgG-CsgF complex and how these impact ssDNA, water and ion movement. We find that the barrel of CsgG is more susceptible to damage from external electric fields compared to the protein vestibule. Furthermore, the presence of CsgF within the CsgG-CsgF complex enables the complex to withstand higher electric fields. We find that the eyelet loops of CsgG play a key role in both slowing the translocation rate of DNA and modulating the conductance of the pore. CsgF also impacts the DNA translocation rate, but to a lesser degree than CsgG.
    Schlagwörter Escherichia coli ; biotechnology ; membrane proteins ; molecular dynamics ; nanopores ; strength (mechanics)
    Sprache Englisch
    Umfang p. 6417-6430.
    Erscheinungsort Elsevier B.V.
    Dokumenttyp Artikel
    ZDB-ID 2694435-2
    ISSN 2001-0370
    ISSN 2001-0370
    DOI 10.1016/j.csbj.2021.11.014
    Datenquelle NAL Katalog (AGRICOLA)

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  2. Artikel: Corrigendum to "Atomistic level characterisation of ssDNA translocation through the

    Rattu, Punam / Glencross, Flo / Mader, Sophie L / Skylaris, Chris-Kriton / Matthews, Stephen J / Rouse, Sarah L / Khalid, Syma

    Computational and structural biotechnology journal

    2022  Band 20, Seite(n) 1027

    Abstract: This corrects the article DOI: 10.1016/j.csbj.2021.11.014.]. ...

    Abstract [This corrects the article DOI: 10.1016/j.csbj.2021.11.014.].
    Sprache Englisch
    Erscheinungsdatum 2022-02-15
    Erscheinungsland Netherlands
    Dokumenttyp Published Erratum
    ZDB-ID 2694435-2
    ISSN 2001-0370
    ISSN 2001-0370
    DOI 10.1016/j.csbj.2022.02.010
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel: Atomistic level characterisation of ssDNA translocation through the

    Rattu, Punam / Glencross, Flo / Mader, Sophie L / Skylaris, Chris-Kriton / Matthews, Stephen J / Rouse, Sarah L / Khalid, Syma

    Computational and structural biotechnology journal

    2021  Band 19, Seite(n) 6417–6430

    Abstract: Two proteins of ... ...

    Abstract Two proteins of the
    Sprache Englisch
    Erscheinungsdatum 2021-11-18
    Erscheinungsland Netherlands
    Dokumenttyp Journal Article
    ZDB-ID 2694435-2
    ISSN 2001-0370
    ISSN 2001-0370
    DOI 10.1016/j.csbj.2021.11.014
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel ; Online: Optical control of ultrafast structural dynamics in a fluorescent protein.

    Hutchison, Christopher D M / Baxter, James M / Fitzpatrick, Ann / Dorlhiac, Gabriel / Fadini, Alisia / Perrett, Samuel / Maghlaoui, Karim / Lefèvre, Salomé Bodet / Cordon-Preciado, Violeta / Ferreira, Josie L / Chukhutsina, Volha U / Garratt, Douglas / Barnard, Jonathan / Galinis, Gediminas / Glencross, Flo / Morgan, Rhodri M / Stockton, Sian / Taylor, Ben / Yuan, Letong /
    Romei, Matthew G / Lin, Chi-Yun / Marangos, Jon P / Schmidt, Marius / Chatrchyan, Viktoria / Buckup, Tiago / Morozov, Dmitry / Park, Jaehyun / Park, Sehan / Eom, Intae / Kim, Minseok / Jang, Dogeun / Choi, Hyeongi / Hyun, HyoJung / Park, Gisu / Nango, Eriko / Tanaka, Rie / Owada, Shigeki / Tono, Kensuke / DePonte, Daniel P / Carbajo, Sergio / Seaberg, Matt / Aquila, Andrew / Boutet, Sebastien / Barty, Anton / Iwata, So / Boxer, Steven G / Groenhof, Gerrit / van Thor, Jasper J

    Nature chemistry

    2023  Band 15, Heft 11, Seite(n) 1607–1615

    Abstract: The photoisomerization reaction of a fluorescent protein chromophore occurs on the ultrafast timescale. The structural dynamics that result from femtosecond optical excitation have contributions from vibrational and electronic processes and from reaction ...

    Abstract The photoisomerization reaction of a fluorescent protein chromophore occurs on the ultrafast timescale. The structural dynamics that result from femtosecond optical excitation have contributions from vibrational and electronic processes and from reaction dynamics that involve the crossing through a conical intersection. The creation and progression of the ultrafast structural dynamics strongly depends on optical and molecular parameters. When using X-ray crystallography as a probe of ultrafast dynamics, the origin of the observed nuclear motions is not known. Now, high-resolution pump-probe X-ray crystallography reveals complex sub-ångström, ultrafast motions and hydrogen-bonding rearrangements in the active site of a fluorescent protein. However, we demonstrate that the measured motions are not part of the photoisomerization reaction but instead arise from impulsively driven coherent vibrational processes in the electronic ground state. A coherent-control experiment using a two-colour and two-pulse optical excitation strongly amplifies the X-ray crystallographic difference density, while it fully depletes the photoisomerization process. A coherent control mechanism was tested and confirmed the wave packets assignment.
    Mesh-Begriff(e) Motion ; Vibration ; Rhodopsin ; Hydrogen Bonding
    Chemische Substanzen Rhodopsin (9009-81-8)
    Sprache Englisch
    Erscheinungsdatum 2023-08-10
    Erscheinungsland England
    Dokumenttyp Journal Article
    ZDB-ID 2464596-5
    ISSN 1755-4349 ; 1755-4330
    ISSN (online) 1755-4349
    ISSN 1755-4330
    DOI 10.1038/s41557-023-01275-1
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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