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  1. Article ; Online: Spatiotemporal-resolved protein networks profiling with photoactivation dependent proximity labeling.

    Zhai, Yansheng / Huang, Xiaoyan / Zhang, Keren / Huang, Yuchen / Jiang, Yanlong / Cui, Jingwei / Zhang, Zhe / Chiu, Cookson K C / Zhong, Weiye / Li, Gang

    Nature communications

    2022  Volume 13, Issue 1, Page(s) 4906

    Abstract: Enzymatic-based proximity labeling approaches based on activated esters or phenoxy radicals have been widely used for mapping subcellular proteome and protein interactors in living cells. However, activated esters are poorly reactive which leads to a ... ...

    Abstract Enzymatic-based proximity labeling approaches based on activated esters or phenoxy radicals have been widely used for mapping subcellular proteome and protein interactors in living cells. However, activated esters are poorly reactive which leads to a wide labeling radius and phenoxy radicals generated by peroxide treatment may disturb redox-sensitive pathways. Herein, we report a photoactivation-dependent proximity labeling (PDPL) method designed by genetically attaching photosensitizer protein miniSOG to a protein of interest. Triggered by blue light and tunned by irradiation time, singlet oxygen is generated, thereafter enabling spatiotemporally-resolved aniline probe labeling of histidine residues. We demonstrate its high-fidelity through mapping of organelle-specific proteomes. Side-by-side comparison of PDPL with TurboID reveals more specific and deeper proteomic coverage by PDPL. We further apply PDPL to the disease-related transcriptional coactivator BRD4 and E3 ligase Parkin, and discover previously unknown interactors. Through over-expression screening, two unreported substrates Ssu72 and SNW1 are identified for Parkin, whose degradation processes are mediated by the ubiquitination-proteosome pathway.
    MeSH term(s) Esters ; Nuclear Proteins ; Proteome/metabolism ; Proteomics/methods ; Transcription Factors ; Ubiquitin-Protein Ligases
    Chemical Substances Esters ; Nuclear Proteins ; Proteome ; Transcription Factors ; Ubiquitin-Protein Ligases (EC 2.3.2.27)
    Language English
    Publishing date 2022-08-20
    Publishing country England
    Document type Journal Article ; 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/s41467-022-32689-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Does deamidation affect inhibitory mechanisms towards amyloid protein aggregation?

    Lam, Yuko P Y / Chiu, Cookson K C / Wootton, Christopher A / Hands-Portman, Ian / Li, Meng / Barrow, Mark P / O'Connor, Peter B

    Chemical communications (Cambridge, England)

    2020  Volume 56, Issue 68, Page(s) 9787–9790

    Abstract: Deamidated amyloid proteins have been shown to accelerate fibril formation. Herein, the results show the inhibition performance and the interaction site between site-specific inhibitor and amyloid protein are significantly influenced by deamidation; ... ...

    Abstract Deamidated amyloid proteins have been shown to accelerate fibril formation. Herein, the results show the inhibition performance and the interaction site between site-specific inhibitor and amyloid protein are significantly influenced by deamidation; while the inhibition mechanism of non-site specific inhibitor shows no significant disruption caused by amyloid protein deamidation.
    MeSH term(s) Amino Acid Sequence ; Amyloid/chemistry ; Amyloid/metabolism ; Catechin/analogs & derivatives ; Catechin/chemistry ; Catechin/metabolism ; Catechin/pharmacology ; Humans ; Islet Amyloid Polypeptide/chemistry ; Islet Amyloid Polypeptide/metabolism ; Microscopy, Electron, Transmission ; Protein Aggregates/drug effects ; Spectrometry, Fluorescence
    Chemical Substances Amyloid ; Islet Amyloid Polypeptide ; Protein Aggregates ; Catechin (8R1V1STN48) ; epigallocatechin gallate (BQM438CTEL)
    Language English
    Publishing date 2020-08-03
    Publishing country England
    Document type Journal Article
    ZDB-ID 1472881-3
    ISSN 1364-548X ; 1359-7345 ; 0009-241X
    ISSN (online) 1364-548X
    ISSN 1359-7345 ; 0009-241X
    DOI 10.1039/d0cc03548c
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Metallocomplex-Peptide Interactions Studied by Ultrahigh Resolution Mass Spectrometry.

    Chiu, Cookson K C / Lam, Yuko P Y / Wootton, Christopher A / Barrow, Mark P / Sadler, Peter J / O'Connor, Peter B

    Journal of the American Society for Mass Spectrometry

    2020  Volume 31, Issue 3, Page(s) 594–601

    Abstract: ... The ... ...

    Abstract The Os
    MeSH term(s) Amino Acid Sequence ; Animals ; Antineoplastic Agents/chemistry ; Antineoplastic Agents/metabolism ; Binding Sites ; Cattle ; Coordination Complexes/chemistry ; Coordination Complexes/metabolism ; Models, Molecular ; Osmium/chemistry ; Osmium/metabolism ; Peptides/chemistry ; Peptides/metabolism ; Protein Binding ; Serum Albumin, Bovine/chemistry ; Serum Albumin, Bovine/metabolism ; Tandem Mass Spectrometry/methods
    Chemical Substances Antineoplastic Agents ; Coordination Complexes ; Peptides ; Serum Albumin, Bovine (27432CM55Q) ; Osmium (2E7M255OPY)
    Language English
    Publishing date 2020-02-24
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1073671-2
    ISSN 1879-1123 ; 1044-0305
    ISSN (online) 1879-1123
    ISSN 1044-0305
    DOI 10.1021/jasms.9b00054
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Metallation-Induced Heterogeneous Dynamics of DNA Revealed by Single-Molecule FRET.

    Berrocal-Martin, Raul / Sanchez-Cano, Carlos / Chiu, Cookson K C / Needham, Russell J / Sadler, Peter J / Magennis, Steven W

    Chemistry (Weinheim an der Bergstrasse, Germany)

    2020  Volume 26, Issue 22, Page(s) 4980–4987

    Abstract: The metallation of nucleic acids is key to wide-ranging applications, from anticancer medicine to nanomaterials, yet there is a lack of understanding of the molecular-level effects of metallation. Here, we apply single-molecule fluorescence methods to ... ...

    Abstract The metallation of nucleic acids is key to wide-ranging applications, from anticancer medicine to nanomaterials, yet there is a lack of understanding of the molecular-level effects of metallation. Here, we apply single-molecule fluorescence methods to study the reaction of an organo-osmium anticancer complex and DNA. Individual metallated DNA hairpins are characterised using Förster resonance energy transfer (FRET). Although ensemble measurements suggest a simple two-state system, single-molecule experiments reveal an underlying heterogeneity in the oligonucleotide dynamics, attributable to different degrees of metallation of the GC-rich hairpin stem. Metallated hairpins display fast two-state transitions with a two-fold increase in the opening rate to ≈2 s
    MeSH term(s) Antineoplastic Agents/chemistry ; Antineoplastic Agents/pharmacology ; DNA/chemistry ; DNA/metabolism ; Fluorescence ; Fluorescence Resonance Energy Transfer ; Nanotechnology ; Nucleic Acid Conformation
    Chemical Substances Antineoplastic Agents ; DNA (9007-49-2)
    Language English
    Publishing date 2020-03-09
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 1478547-X
    ISSN 1521-3765 ; 0947-6539
    ISSN (online) 1521-3765
    ISSN 0947-6539
    DOI 10.1002/chem.202000458
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Does deamidation affect inhibitory mechanisms towards amyloid protein aggregation?

    Lam, Yuko P. Y. / Chiu, Cookson K. C. / Wootton, Christopher A. / Hands-Portman, Ian / Li, Meng / Barrow, Mark P. / O'Connor, Peter B.

    Chemical communications. 2020 Aug. 25, v. 56, no. 68

    2020  

    Abstract: Deamidated amyloid proteins have been shown to accelerate fibril formation. Herein, the results show the inhibition performance and the interaction site between site-specific inhibitor and amyloid protein are significantly influenced by deamidation; ... ...

    Abstract Deamidated amyloid proteins have been shown to accelerate fibril formation. Herein, the results show the inhibition performance and the interaction site between site-specific inhibitor and amyloid protein are significantly influenced by deamidation; while the inhibition mechanism of non-site specific inhibitor shows no significant disruption caused by amyloid protein deamidation.
    Keywords amyloid ; chemical communication ; deamidation
    Language English
    Dates of publication 2020-0825
    Size p. 9787-9790.
    Publishing place The Royal Society of Chemistry
    Document type Article
    ZDB-ID 1472881-3
    ISSN 1364-548X ; 1359-7345 ; 0009-241X
    ISSN (online) 1364-548X
    ISSN 1359-7345 ; 0009-241X
    DOI 10.1039/d0cc03548c
    Database NAL-Catalogue (AGRICOLA)

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  6. Article ; Online: Determination of the Aggregate Binding Site of Amyloid Protofibrils Using Electron Capture Dissociation Tandem Mass Spectrometry.

    Lam, Yuko P Y / Wootton, Christopher A / Hands-Portman, Ian / Wei, Juan / Chiu, Cookson K C / Romero-Canelon, I / Lermyte, Frederik / Barrow, Mark P / O'Connor, Peter B

    Journal of the American Society for Mass Spectrometry

    2020  Volume 31, Issue 2, Page(s) 267–276

    Abstract: Amyloid fibril formation is a hallmark in a range of human diseases. Analysis of the molecular details of amyloid aggregation, however, is limited by the difficulties in solubilizing, separating, and identifying the aggregated biomolecules. Additional ... ...

    Abstract Amyloid fibril formation is a hallmark in a range of human diseases. Analysis of the molecular details of amyloid aggregation, however, is limited by the difficulties in solubilizing, separating, and identifying the aggregated biomolecules. Additional labeling or protein modification is required in many current analytical techniques in order to provide molecular details of amyloid protein aggregation, but these modifications may result in protein structure disruption. Herein, ultrahigh resolution mass spectrometry (MS) with electron capture dissociation tandem MS (ECD MS/MS) has been applied to monitor the formation of early oligomers of human islet amyloid polypeptide (hIAPP), which aggregate rapidly in the pancreas of type II diabetes (T2D) patients. ECD MS/MS results show the aggregation region of the early oligomers is at the Ser-28/Ser-29 residue of a hIAPP unit and at the Asn-35 residue of another hIAPP unit near the C-terminus in the gas phase. These data contribute to the understanding of the binding site between hIAPP units which may help for specific target region therapeutic development in the future. Furthermore, MS has also been applied to quantify the amount of soluble amyloid protein remaining in the incubated solutions, which can be used to estimate the aggregation rate of amyloid protein during incubation (28 days). These data are further correlated with the results obtained using fluorescence spectroscopy and transmission electron microscopy (TEM) to generate a general overview of amyloid protein aggregation. The methods demonstrated in this article not only explore the aggregation site of hIAPP down to an amino acid residue level, but are also applicable to many amyloid protein aggregation studies.
    MeSH term(s) Amyloid/chemistry ; Amyloid/ultrastructure ; Binding Sites/physiology ; Humans ; Islet Amyloid Polypeptide/chemistry ; Islet Amyloid Polypeptide/ultrastructure ; Models, Molecular ; Protein Multimerization ; Solubility ; Tandem Mass Spectrometry/methods
    Chemical Substances Amyloid ; Islet Amyloid Polypeptide
    Language English
    Publishing date 2020-01-10
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1073671-2
    ISSN 1879-1123 ; 1044-0305
    ISSN (online) 1879-1123
    ISSN 1044-0305
    DOI 10.1021/jasms.9b00053
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Strained alkynes derived from 2,2'-dihydroxy-1,1'-biaryls; synthesis and copper-free cycloaddition with azides.

    Del Grosso, Alessandro / Galanopoulos, Lavrentis-Dimitrios / Chiu, Cookson K C / Clarkson, Guy J / O Connor, Peter B / Wills, Martin

    Organic & biomolecular chemistry

    2017  Volume 15, Issue 21, Page(s) 4517–4521

    Abstract: A series of strained alkynes were prepared from 2,2'-dihydroxy-biaryls. Several were characterised by X-ray crystallography, revealing strained C(sp)-C(sp)-C( ... ...

    Abstract A series of strained alkynes were prepared from 2,2'-dihydroxy-biaryls. Several were characterised by X-ray crystallography, revealing strained C(sp)-C(sp)-C(sp
    Language English
    Publishing date 2017-05-31
    Publishing country England
    Document type Journal Article
    ZDB-ID 2097583-1
    ISSN 1477-0539 ; 1477-0520
    ISSN (online) 1477-0539
    ISSN 1477-0520
    DOI 10.1039/c7ob00991g
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Structural analysis of peptides modified with organo-iridium complexes, opportunities from multi-mode fragmentation.

    Wootton, Christopher A / Millett, Adam J / Lopez-Clavijo, Andrea F / Chiu, Cookson K C / Barrow, Mark P / Clarkson, Guy J / Sadler, Peter J / O'Connor, Peter B

    The Analyst

    2019  Volume 144, Issue 5, Page(s) 1575–1581

    Abstract: The most widely used anticancer drugs are platinum complexes, but complexes of other transition metals also show promise and may widen the spectrum of activity, reduce side-effects, and overcome resistance. The latter include organo-iridium(iii) 'piano- ... ...

    Abstract The most widely used anticancer drugs are platinum complexes, but complexes of other transition metals also show promise and may widen the spectrum of activity, reduce side-effects, and overcome resistance. The latter include organo-iridium(iii) 'piano-stool' complexes. To understand their mechanism of action, it is important to discover how they bind to biomolecules and how binding is affected by functionalisation of the ligands bound to iridium. We have characterised, by MS and MS/MS techniques, unusual adducts from reactions between 3 novel iridium(iii) anti-cancer complexes each possessing reactive sites both at the metal (coordination by substitution of a labile chlorido ligand) and on the ligand (covalent bond formation involving imine formation by one or two aldehyde functions). Peptide modification by the metal complex had a drastic effect on both Collisonally Activated Dissociation (CAD) and Electron Capture Dissociation (ECD) MS/MS behaviour, tuning requirements, and fragmentation channels. CAD MS/MS was effective only when studying the covalent condensation products. ECD MS/MS, although hindered by electron-quenching at the Iridium complex site, was suitable for studying many of the species observed, locating the modification sites, and often identifying them to within a single amino acid residue.
    Language English
    Publishing date 2019-02-06
    Publishing country England
    Document type Journal Article
    ZDB-ID 210747-8
    ISSN 1364-5528 ; 0003-2654
    ISSN (online) 1364-5528
    ISSN 0003-2654
    DOI 10.1039/c8an02094a
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Does deamidation of islet amyloid polypeptide accelerate amyloid fibril formation?

    Lam, Yuko P Y / Wootton, Christopher A / Hands-Portman, Ian / Wei, Juan / Chiu, Cookson K C / Romero-Canelon, Isolda / Lermyte, Frederik / Barrow, Mark P / O'Connor, Peter B

    Chemical communications (Cambridge, England)

    2018  Volume 54, Issue 98, Page(s) 13853–13856

    Abstract: Mass spectrometry has been applied to determine the deamidation sites and the aggregation region of the deamidated human islet amyloid polypeptide (hIAPP). Mutant hIAPP with iso-aspartic residue mutations at possible deamidation sites showed very ... ...

    Abstract Mass spectrometry has been applied to determine the deamidation sites and the aggregation region of the deamidated human islet amyloid polypeptide (hIAPP). Mutant hIAPP with iso-aspartic residue mutations at possible deamidation sites showed very different fibril formation behaviour, which correlates with the observed deamidation-induced acceleration of hIAPP aggregation.
    MeSH term(s) Amides/chemistry ; Amino Acid Sequence ; Amyloid/chemistry ; Amyloid/genetics ; Amyloid/ultrastructure ; Humans ; Islet Amyloid Polypeptide/chemistry ; Islet Amyloid Polypeptide/genetics ; Islet Amyloid Polypeptide/ultrastructure ; Isoaspartic Acid/chemistry ; Isoaspartic Acid/genetics ; Point Mutation ; Protein Aggregates
    Chemical Substances Amides ; Amyloid ; Islet Amyloid Polypeptide ; Isoaspartic Acid ; Protein Aggregates
    Language English
    Publishing date 2018-11-22
    Publishing country England
    Document type Journal Article
    ZDB-ID 1472881-3
    ISSN 1364-548X ; 1359-7345 ; 0009-241X
    ISSN (online) 1364-548X
    ISSN 1359-7345 ; 0009-241X
    DOI 10.1039/c8cc06675b
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Organoiridium Photosensitizers Induce Specific Oxidative Attack on Proteins within Cancer Cells.

    Zhang, Pingyu / Chiu, Cookson K C / Huang, Huaiyi / Lam, Yuko P Y / Habtemariam, Abraha / Malcomson, Thomas / Paterson, Martin J / Clarkson, Guy J / O'Connor, Peter B / Chao, Hui / Sadler, Peter J

    Angewandte Chemie (International ed. in English)

    2017  Volume 56, Issue 47, Page(s) 14898–14902

    Abstract: Strongly luminescent iridium(III) complexes, [Ir(C,N) ...

    Abstract Strongly luminescent iridium(III) complexes, [Ir(C,N)
    MeSH term(s) A549 Cells ; Chelating Agents/chemistry ; Crystallography, X-Ray ; Density Functional Theory ; Glycolysis ; Histidine/chemistry ; Humans ; Iridium/chemistry ; Ligands ; Luminescence ; Neoplasm Proteins/chemistry ; Neoplasm Proteins/metabolism ; Organometallic Compounds/chemistry ; Organometallic Compounds/pharmacology ; Oxidation-Reduction ; Oxidative Stress/drug effects ; Photochemical Processes ; Photosensitizing Agents/pharmacology ; Quinolines/chemistry ; Spheroids, Cellular/drug effects
    Chemical Substances Chelating Agents ; Ligands ; Neoplasm Proteins ; Organometallic Compounds ; Photosensitizing Agents ; Quinolines ; Iridium (44448S9773) ; Histidine (4QD397987E)
    Language English
    Publishing date 2017-10-19
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2011836-3
    ISSN 1521-3773 ; 1433-7851
    ISSN (online) 1521-3773
    ISSN 1433-7851
    DOI 10.1002/anie.201709082
    Database MEDical Literature Analysis and Retrieval System OnLINE

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