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  1. Article: Nondestructive Microanalysis of Thin-Film Coatings on Historic Metal Threads

    Popowich, Aleksandra / Lam, Thomas / Vicenzi, Edward P.

    Analytical chemistry. 2021 Sept. 15, v. 93, no. 38

    2021  

    Abstract: A new standards-based scanning electron microscopy with the energy-dispersive X-ray spectrometry (SEM–EDS) quantification method was used to analyze the thin-film coating of an 18th century French textile decorated with metal threads in variable pressure ...

    Abstract A new standards-based scanning electron microscopy with the energy-dispersive X-ray spectrometry (SEM–EDS) quantification method was used to analyze the thin-film coating of an 18th century French textile decorated with metal threads in variable pressure conditions. This analytical technique can allow for nondestructive quantitative characterization of the near surface of cultural heritage objects small enough to be placed in an SEM chamber that may contain corrosion products, without applying a conductive coating. A multivoltage analysis consisting of measurements taken at a series of electron beam energies was obtained and input into a film thickness and composition (FTC) computational model to characterize a layered Au on Ag reference material, in addition to a historic metal thread. Using the FTC computation, the thread coating was determined to be an alloy ≈ 80% Au 20% Ag on a nominally pure Ag substrate, and this composition matches a minimum gold standard allowed for goods around the time of manufacture. The computed gilding thicknesses range from single digit nm to 300 nm depending upon surface inhomogeneities formed during the production of the thread. Interaction volumes and X-ray spectra generated by Monte Carlo modeling are consistent with the measured gilding thicknesses and compositions. Validation of the FTC-computed gilding composition and thickness variations were obtained by cross-sectional analysis.
    Keywords X-radiation ; alloys ; analytical chemistry ; bioinformatics ; corrosion ; cross-sectional studies ; cultural heritage ; fabrics ; manufacturing ; spectroscopy
    Language English
    Dates of publication 2021-0915
    Size p. 12906-12913.
    Publishing place American Chemical Society
    Document type Article
    ZDB-ID 1508-8
    ISSN 1520-6882 ; 0003-2700
    ISSN (online) 1520-6882
    ISSN 0003-2700
    DOI 10.1021/acs.analchem.1c02054
    Database NAL-Catalogue (AGRICOLA)

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  2. Article ; Online: Nondestructive Microanalysis of Thin-Film Coatings on Historic Metal Threads.

    Popowich, Aleksandra / Lam, Thomas / Vicenzi, Edward P

    Analytical chemistry

    2021  Volume 93, Issue 38, Page(s) 12906–12913

    Abstract: A new standards-based scanning electron microscopy with the energy-dispersive X-ray spectrometry (SEM-EDS) quantification method was used to analyze the thin-film coating of an 18th century French textile decorated with metal threads in variable pressure ...

    Abstract A new standards-based scanning electron microscopy with the energy-dispersive X-ray spectrometry (SEM-EDS) quantification method was used to analyze the thin-film coating of an 18th century French textile decorated with metal threads in variable pressure conditions. This analytical technique can allow for nondestructive quantitative characterization of the near surface of cultural heritage objects small enough to be placed in an SEM chamber that may contain corrosion products, without applying a conductive coating. A multivoltage analysis consisting of measurements taken at a series of electron beam energies was obtained and input into a film thickness and composition (FTC) computational model to characterize a layered Au on Ag reference material, in addition to a historic metal thread. Using the FTC computation, the thread coating was determined to be an alloy ≈ 80% Au 20% Ag on a nominally pure Ag substrate, and this composition matches a minimum gold standard allowed for goods around the time of manufacture. The computed gilding thicknesses range from single digit nm to 300 nm depending upon surface inhomogeneities formed during the production of the thread. Interaction volumes and X-ray spectra generated by Monte Carlo modeling are consistent with the measured gilding thicknesses and compositions. Validation of the FTC-computed gilding composition and thickness variations were obtained by cross-sectional analysis.
    Language English
    Publishing date 2021-09-15
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1508-8
    ISSN 1520-6882 ; 0003-2700
    ISSN (online) 1520-6882
    ISSN 0003-2700
    DOI 10.1021/acs.analchem.1c02054
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Native triboelectric nanogenerator ion mobility-mass spectrometry of egg proteins relevant to objects of cultural heritage at picoliter and nanomolar quantities.

    Vallejo, Daniel D / Popowich, Aleksandra / Arslanoglu, Julie / Tokarski, Caroline / Fernández, Facundo M

    Analytica chimica acta

    2023  Volume 1269, Page(s) 341374

    MeSH term(s) Mass Spectrometry/methods ; Egg Proteins ; Ion Mobility Spectrometry/methods
    Chemical Substances Egg Proteins
    Language English
    Publishing date 2023-05-22
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 1483436-4
    ISSN 1873-4324 ; 0003-2670
    ISSN (online) 1873-4324
    ISSN 0003-2670
    DOI 10.1016/j.aca.2023.341374
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Species identification of ivory and bone museum objects using minimally invasive proteomics.

    Gilbert, Catherine / Krupicka, Vaclav / Galluzzi, Francesca / Popowich, Aleksandra / Bathany, Katell / Claverol, Stéphane / Arslanoglu, Julie / Tokarski, Caroline

    Science advances

    2024  Volume 10, Issue 4, Page(s) eadi9028

    Abstract: Ivory is a highly prized material in many cultures since it can be carved into intricate designs and have a highly polished surface. Due to its popularity, the animals from which ivory can be sourced are under threat of extinction. Identification of ... ...

    Abstract Ivory is a highly prized material in many cultures since it can be carved into intricate designs and have a highly polished surface. Due to its popularity, the animals from which ivory can be sourced are under threat of extinction. Identification of ivory species is not only important for CITES compliance, it can also provide information about the context in which a work was created. Here, we have developed a minimally invasive workflow to remove minimal amounts of material from precious objects and, using high-resolution mass spectrometry-based proteomics, identified the taxonomy of ivory and bone objects from The Metropolitan Museum of Art collection dating from as early as 4000 B.C. We built a proteomic database of underrepresented species based on exemplars from the American Museum of Natural History, and proposed alternative data analysis workflows for samples containing inconsistently preserved organic material. This application demonstrates extensive ivory species identification using proteomics to unlock sequence uncertainties, e.g., Leu/Ile discrimination.
    MeSH term(s) Animals ; Conservation of Natural Resources ; Museums ; Proteomics ; Bone and Bones ; Mass Spectrometry
    Language English
    Publishing date 2024-01-26
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2810933-8
    ISSN 2375-2548 ; 2375-2548
    ISSN (online) 2375-2548
    ISSN 2375-2548
    DOI 10.1126/sciadv.adi9028
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Removal of nanoparticles by coagulation.

    Popowich, Aleksandra / Zhang, Qi / Le, X Chris

    Journal of environmental sciences (China)

    2015  Volume 38, Page(s) 168–171

    MeSH term(s) Humic Substances ; Nanoparticles/chemistry ; Nanotubes, Carbon/chemistry ; Osmolar Concentration ; Water Purification
    Chemical Substances Humic Substances ; Nanotubes, Carbon
    Language English
    Publishing date 2015-12
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1092300-7
    ISSN 1878-7320 ; 1001-0742
    ISSN (online) 1878-7320
    ISSN 1001-0742
    DOI 10.1016/j.jes.2015.10.001
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: p-Azidophenylarsenoxide: An Arsenical "Bait" for the In Situ Capture and Identification of Cellular Arsenic-Binding Proteins.

    Yan, Xiaowen / Li, Jinhua / Liu, Qingqing / Peng, Hanyong / Popowich, Aleksandra / Wang, Zhixin / Li, Xing-Fang / Le, X Chris

    Angewandte Chemie (International ed. in English)

    2016  Volume 55, Issue 45, Page(s) 14051–14056

    Abstract: Identification of arsenic-binding proteins is important for understanding arsenic health effects and for developing arsenic-based therapeutics. We report here a strategy for the capture and identification of arsenic-binding proteins in living cells. We ... ...

    Abstract Identification of arsenic-binding proteins is important for understanding arsenic health effects and for developing arsenic-based therapeutics. We report here a strategy for the capture and identification of arsenic-binding proteins in living cells. We designed an azide-labeled arsenical, p-azidophenylarsenoxide (PAzPAO), to serve bio-orthogonal functions: the trivalent arsenical group binds to cellular proteins in situ, and the azide group facilitates click chemistry with dibenzylcyclooctyne. The selective and efficient capture of arsenic-binding proteins enables subsequent enrichment and identification by shotgun proteomics. Applications of the technique are demonstrated using the A549 human lung carcinoma cells and two in vitro model systems. The technique enables the capture and identification of 48 arsenic-binding proteins in A549 cells incubated with PAzPAO. Among the identified proteins are a series of antioxidant proteins (e.g., thioredoxin, peroxiredoxin, peroxide reductase, glutathione reductase, and protein disulfide isomerase) and glyceraldehyde-3-phosphate dehydrogenase. Identification of these functional proteins, along with studies of arsenic binding and enzymatic inhibition, points to these proteins as potential molecular targets that play important roles in arsenic-induced health effects and in cancer treatment.
    MeSH term(s) Arsenic/analysis ; Arsenicals/chemical synthesis ; Arsenicals/chemistry ; Azides/chemical synthesis ; Azides/chemistry ; Carrier Proteins/analysis ; Cell Line, Tumor ; Click Chemistry ; Humans ; Models, Molecular ; Molecular Structure
    Chemical Substances Arsenicals ; Azides ; Carrier Proteins ; p-azidophenylarsenoxide ; Arsenic (N712M78A8G)
    Language English
    Publishing date 2016-10-10
    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.201608006
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Methylated and thiolated arsenic species for environmental and health research - A review on synthesis and characterization.

    Cullen, William R / Liu, Qingqing / Lu, Xiufen / McKnight-Whitford, Anthony / Peng, Hanyong / Popowich, Aleksandra / Yan, Xiaowen / Zhang, Qi / Fricke, Michael / Sun, Hongsui / Le, X Chris

    Journal of environmental sciences (China)

    2016  Volume 49, Page(s) 7–27

    Abstract: Hundreds of millions of people around the world are exposed to elevated concentrations of inorganic and organic arsenic compounds, increasing the risk of a wide range of health effects. Studies of the environmental fate and human health effects of ... ...

    Abstract Hundreds of millions of people around the world are exposed to elevated concentrations of inorganic and organic arsenic compounds, increasing the risk of a wide range of health effects. Studies of the environmental fate and human health effects of arsenic require authentic arsenic compounds. We summarize here the synthesis and characterization of more than a dozen methylated and thiolated arsenic compounds that are not commercially available. We discuss the methods of synthesis for the following 14 trivalent (III) and pentavalent (V) arsenic compounds: monomethylarsonous acid (MMA
    MeSH term(s) Arsenic/chemistry ; Arsenicals/chemistry ; Chemical Safety ; Ecology ; Environmental Health ; Hazardous Substances/chemistry
    Chemical Substances Arsenicals ; Hazardous Substances ; Arsenic (N712M78A8G)
    Language English
    Publishing date 2016-11
    Publishing country Netherlands
    Document type Journal Article ; Review
    ZDB-ID 1092300-7
    ISSN 1878-7320 ; 1001-0742
    ISSN (online) 1878-7320
    ISSN 1001-0742
    DOI 10.1016/j.jes.2016.11.004
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Therapeutic and analytical applications of arsenic binding to proteins.

    Chen, Beibei / Liu, Qingqing / Popowich, Aleksandra / Shen, Shengwen / Yan, Xiaowen / Zhang, Qi / Li, Xing-Fang / Weinfeld, Michael / Cullen, William R / Le, X Chris

    Metallomics : integrated biometal science

    2015  Volume 7, Issue 1, Page(s) 39–55

    Abstract: Arsenic binding to proteins plays a pivotal role in the health effects of arsenic. Further knowledge of arsenic binding to proteins will advance the development of bioanalytical techniques and therapeutic drugs. This review summarizes recent work on ... ...

    Abstract Arsenic binding to proteins plays a pivotal role in the health effects of arsenic. Further knowledge of arsenic binding to proteins will advance the development of bioanalytical techniques and therapeutic drugs. This review summarizes recent work on arsenic-based drugs, imaging of cellular events, capture and purification of arsenic-binding proteins, and biosensing of arsenic. Binding of arsenic to the promyelocytic leukemia fusion oncoprotein (PML-RARα) is a plausible mode of action leading to the successful treatment of acute promyelocytic leukemia (APL). Identification of other oncoproteins critical to other cancers and the development of various arsenicals and targeted delivery systems are promising approaches to the treatment of other types of cancers. Techniques for capture, purification, and identification of arsenic-binding proteins make use of specific binding between trivalent arsenicals and the thiols in proteins. Biarsenical probes, such as FlAsH-EDT2 and ReAsH-EDT2, coupled with tetracysteine tags that are genetically incorporated into the target proteins, are used for site-specific fluorescence labelling and imaging of the target proteins in living cells. These allow protein dynamics and protein-protein interactions to be studied. Arsenic affinity chromatography is useful for purification of thiol-containing proteins, and its combination with mass spectrometry provides a targeted proteomic approach for studying the interactions between arsenicals and proteins in cells. Arsenic biosensors evolved from the knowledge of arsenic resistance and arsenic binding to proteins in bacteria, and have now been developed into analytical techniques that are suitable for the detection of arsenic in the field. Examples in the four areas, arsenic-based drugs, imaging of cellular events, purification of specific proteins, and arsenic biosensors, demonstrate important therapeutic and analytical applications of arsenic protein binding.
    MeSH term(s) Animals ; Arsenic/chemistry ; Arsenic/metabolism ; Arsenicals/chemistry ; Arsenicals/metabolism ; Biosensing Techniques ; Cell Line, Tumor ; Chromatography, Affinity ; Humans ; Mass Spectrometry ; Mice ; Protein Binding ; Proteomics/methods ; Recombinant Fusion Proteins/chemistry ; Recombinant Fusion Proteins/metabolism
    Chemical Substances Arsenicals ; Recombinant Fusion Proteins ; Arsenic (N712M78A8G)
    Language English
    Publishing date 2015-01
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2474317-3
    ISSN 1756-591X ; 1756-5901
    ISSN (online) 1756-591X
    ISSN 1756-5901
    DOI 10.1039/c4mt00222a
    Database MEDical Literature Analysis and Retrieval System OnLINE

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