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2D/3D Metallic Nano-objects Self-Organized in an Organic Molecular Thin Film
We present the fabrication and investigation of the properties of nanocomposite structures consisting of two-dimensional (2D) and three-dimensional (3D) metallic nano-objects self-organized on the surface and inside of organic molecular thin-film copper tetrafluorophthalocyanine (CuPcF4). Metallic atoms, deposited under ultrahigh vacuum (UHV) conditions onto the organic ultrathin film, diffuse along the surface and self-assemble into a system of 2D metallic overlayers. At the same time, the majority of the metal atoms diffuse into the organic matrix and self-organize into 3D nanoparticles (NPs) in a well-defined manner. The evolution of the morphology and electronic properties of such structures as a function of nominal metal content is studied under UHV conditions using transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HR-TEM), and photoelectron spectroscopy (PES) techniques. Using HR-TEM, we have observed the periodicity of atomic planes of individual silver NPs. The steady formation of agglomerates from individual single nanocrystallites with intercrystallite boundaries is observed as well. PES reveals generally weak chemical interactions between silver and the organic matrix and n-doping of CuPcF4 at the initial stages of silver deposition, which is associated with charge transfer from the 2D wetting layer on the basis of core-level spectra shift analysis. Copyright Β© 2020 American Chemical Society
North Pacific versus North Atlantic: a case with species of the amphiboreal littoral mite genus Thalassogamasus gen. nov. (Parasitifomes, Mesostigmata Parasitidae)
Makarova, Olga L. (2019): North Pacific versus North Atlantic: a case with species of the amphiboreal littoral mite genus Thalassogamasus gen. nov. (Parasitifomes, Mesostigmata Parasitidae). Zootaxa 4647 (1): 457-485, DOI: https://doi.org/10.11646/zootaxa.4647.1.2
Description of Oromurcia magadanensis sp. nov. (Acari, Oribatida, Ceratozetidae) from Russia, with remarks on biogeography of the genus Oromurcia Thor, 1930
Ermilov, Sergey G., Makarova, Olga L., Behan-Pelletier, Valerie M. (2022): Description of Oromurcia magadanensis sp. nov. (Acari, Oribatida, Ceratozetidae) from Russia, with remarks on biogeography of the genus Oromurcia Thor, 1930. Zootaxa 5187 (1): 30-52, DOI: https://doi.org/10.11646/zootaxa.5187.1.
Human U4/U6.U5 and U4atac/U6atac.U5 Tri-snRNPs Exhibit Similar Protein Compositions
In the U12-dependent spliceosome, the U4atac/U6atac snRNP represents the functional analogue of the major U4/U6 snRNP. Little information is available presently regarding the protein composition of the former snRNP and its association with other snRNPs. In this report we show that human U4atac/U6atac di-snRNPs associate with U5 snRNPs to form a 25S U4atac/U6atac.U5 trimeric particle. Comparative analysis of minor and major tri-snRNPs by using immunoprecipitation experiments revealed that their protein compositions are very similar, if not identical. Not only U5-specific proteins but, surprisingly, all tested U4/U6- and major tri-snRNP-specific proteins were detected in the minor tri-snRNP complex. Significantly, the major tri-snRNP-specific proteins 65K and 110K, which are required for integration of the major tri-snRNP into the U2-dependent spliceosome, were among those proteins detected in the minor tri-snRNP, raising an interesting question as to how the specificity of addition of tri-snRNP to the corresponding spliceosome is maintained. Moreover, immunodepletion studies demonstrated that the U4/U6-specific 61K protein, which is involved in the formation of major tri-snRNPs, is essential for the association of the U4atac/U6atac di-snRNP with U5 to form the U4atac/U6atac.U5 tri-snRNP. Subsequent immunoprecipitation studies demonstrated that those proteins detected in the minor tri-snRNP complex are also incorporated into U12-dependent spliceosomes. This remarkable conservation of polypeptides between minor and major spliceosomes, coupled with the absence of significant sequence similarity between the functionally analogous snRNAs, supports an evolutionary model in which most major and minor spliceosomal proteins, but not snRNAs, are derived from a common ancestor
Rol' disgemoglobinemiy v patogeneze sosudistykh narusheniy u zhenshchin s sakharnym diabetom 2 tipa v period perimenopauzy
Π¦Π΅Π»Ρ. ΠΡΠ΅Π½ΠΊΠ° ΠΎΡΠΎΠ±Π΅Π½Π½ΠΎΡΡΠ΅ΠΉ ΡΡΠ½ΠΊΡΠΈΠΎΠ½ΠΈΡΠΎΠ²Π°Π½ΠΈΡ Π³Π΅ΠΌΠΈΡΠ΅ΡΠΊΠΎΠ³ΠΎ ΠΊΠΎΠΌΠΏΠΎΠ½Π΅Π½ΡΠ° ΠΊΠΈΡΠ»ΠΎ- ΡΠΎΠ΄ΡΡΠ°Π½ΡΠΏΠΎΡΡΠ½ΠΎΠΉ ΡΠΈΡΡΠ΅ΠΌΡ Ρ ΠΆΠ΅Π½ΡΠΈΠ½ Ρ Π‘Π 2 ΡΠΈΠΏΠ° Π² ΠΏΠ΅ΡΠΈΠΎΠ΄ ΠΏΠ΅ΡΠΈΠΌΠ΅Π½ΠΎΠΏΠ°ΡΠ·Ρ.
ΠΠ°ΡΠ΅ΡΠΈΠ°Π»Ρ ΠΈ ΠΌΠ΅ΡΠΎΠ΄Ρ. Π ΠΈΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π½ΠΈΠΈ ΠΏΡΠΈΠ½ΠΈΠΌΠ°Π»ΠΈ ΡΡΠ°ΡΡΠΈΠ΅ 45 ΠΆΠ΅Π½ΡΠΈΠ½ Π² Π²ΠΎΠ·ΡΠ°ΡΡΠ΅ 42- 50 Π»Π΅Ρ. 1-Ρ Π³ΡΡΠΏΠΏΡ ΡΠΎΡΡΠ°Π²ΠΈΠ»ΠΈ 24 ΠΆΠ΅Π½ΡΠΈΠ½Ρ Ρ Π‘Π 2 ΡΠΈΠΏΠ° Π² ΡΠ°Π·Π΅ ΠΏΠ΅ΡΠΈΠΌΠ΅Π½ΠΎΠΏΠ°ΡΠ·Ρ Π² Π²ΠΎΠ·ΡΠ°ΡΡΠ΅ 45-50 Π»Π΅Ρ. ΠΠΎ 2?Ρ Π³ΡΡΠΏΠΏΡ Π²ΠΎΡΠ»Π° 21 ΠΆΠ΅Π½ΡΠΈΠ½Π° Π±Π΅Π· Π‘Π Π² Π²ΠΎΠ·ΡΠ°ΡΡΠ΅ 44-49 Π»Π΅Ρ. ΠΠΎΠ»ΡΠ½ΡΠ΅ ΠΊ ΠΌΠΎΠΌΠ΅Π½ΡΡ ΠΈΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π½ΠΈΠΉ Π½Π°Ρ
ΠΎΠ΄ΠΈΠ»ΠΈΡΡ Π² ΡΠΎΡΡΠΎΡΠ½ΠΈΠΈ ΡΡΠ±ΠΊΠΎΠΌΠΏΠ΅Π½ΡΠ°ΡΠΈΠΈ Π‘Π. ΠΡΠ΅ΠΌ ΠΎΠ±ΡΠ»Π΅Π΄ΡΠ΅ΠΌΡΠΌ (ΠΏ=45) ΠΏΡΠΎΠ²ΠΎΠ΄ΠΈΠ»ΠΎΡΡ ΠΎΠΏΡΠ΅Π΄Π΅Π»Π΅Π½ΠΈΠ΅ Π³Π°Π·ΠΎΠ²ΠΎΠ³ΠΎ ΠΈ ΠΊΠΈΡΠ»ΠΎΡΠ½ΠΎ-ΠΎΡΠ½ΠΎΠ²Π½ΠΎΠ³ΠΎ ΡΠΎΡΡΠ°Π²Π° ΠΊΠ°ΠΏΠΈΠ»Π»ΡΡΠ½ΠΎΠΉ ΠΊΡΠΎΠ²ΠΈ Ρ ΠΎΠ΄Π½ΠΎΠ²ΡΠ΅ΠΌΠ΅Π½Π½ΠΎΠΉ Π‘Π-ΠΎΠΊΡΠΈΠΌΠ΅ΡΡΠΈΠ΅ΠΉ, ΠΎΠΏΡΠ΅Π΄Π΅Π»Π΅Π½ΠΈΠ΅ HbAlc.
Π Π΅Π·ΡΠ»ΡΡΠ°ΡΡ. Π£ΡΠΎΠ²Π΅Π½Ρ HbAlc Ρ ΠΆΠ΅Π½ΡΠΈΠ½, Π±ΠΎΠ»ΡΠ½ΡΡ
Π‘Π 2, ΡΠΈΠΏΠ° ΠΎΠΊΠ°Π·Π°Π»ΡΡ Π² 1.4 ΡΠ°Π·Π° Π²ΡΡΠ΅ Π² ΡΡΠ°Π²Π½Π΅Π½ΠΈΠΈ Ρ ΠΈΡ
Π·Π΄ΠΎΡΠΎΠ²ΡΠΌΠΈ ΡΠ²Π΅ΡΡΡΠ½ΠΈΡΠ°ΠΌΠΈ. ΠΠΊΡΠΈΠ³Π΅ΠΌΠΎΠ³Π»ΠΎΠ±ΠΈΠ½ (O2Hb) Π² Π³ΡΡΠΏΠΏΠ΅ ΠΆΠ΅Π½ΡΠΈΠ½ Ρ Π‘Π 2 ΡΠΈΠΏΠ° ΠΎΠΊΠ°Π·Π°Π»ΡΡ Π½Π΅ΡΠΊΠΎΠ»ΡΠΊΠΎ Π½ΠΈΠΆΠ΅, ΡΠ΅ΠΌ Π² Π³ΡΡΠΏΠΏΠ΅ ΠΊΠΎΠ½ΡΡΠΎΠ»Ρ. ΠΡΠΈ ΡΡΠΎΠΌ ΡΠΎΠ΄Π΅ΡΠΆΠ°Π½ΠΈΠ΅ ΡΡΠ°ΠΊΡΠΈΠΈ Π΄Π΅ΠΎΠΊΡΠΈΠ³Π΅ΠΌΠΎΠ³Π»ΠΎΠ±ΠΈΠ½Π° (ΠHb) ΠΎΠΊΠ°Π·Π°Π»ΠΎΡΡ ΠΎΠ΄ΠΈΠ½Π°ΠΊΠΎΠ²ΡΠΌ Π² ΠΎΠ±Π΅ΠΈΡ
Π³ΡΡΠΏΠΏΠ°Ρ
. ΠΡΠΎΡΠ΅Π½ΡΠ½ΠΎΠ΅ ΡΠΎΠ΄Π΅ΡΠΆΠ°Π½ΠΈΠ΅ ΡΡΠ°ΠΊΡΠΈΠΈ Π‘ΠHb Ρ ΠΆΠ΅Π½ΡΠΈΠ½, Π±ΠΎΠ»ΡΠ½ΡΡ
Π‘Π 2 ΡΠΈΠΏΠ°, ΠΎΠΊΠ°Π·Π°Π»ΠΎΡΡ Π² 2 ΡΠ°Π·Π° Π²ΡΡΠ΅, ΡΠ΅ΠΌ Π² Π³ΡΡΠΏΠΏΠ΅ ΠΊΠΎΠ½ΡΡΠΎΠ»Ρ. ΠΡΠΎΡΠ΅Π½Ρ MetHb Π² ΠΎΠ±Π΅ΠΈΡ
Π³ΡΡΠΏΠΏΠ°Ρ
Π½Π΅ ΠΏΡΠ΅Π²ΡΡΠ°Π» ΡΠΈΠ·ΠΈΠΎΠ»ΠΎΠ³ΠΈΡΠ΅ΡΠΊΠΈΠ΅ Π½ΠΎΡΠΌΡ (Π΄ΠΎ 2%). ΠΠ΄Π½Π°ΠΊΠΎ Ρ ΠΆΠ΅Π½ΡΠΈΠ½ Ρ Π‘Π 2 ΡΠΈΠΏΠ° Π΄Π°Π½Π½ΡΠΉ ΠΏΠΎΠΊΠ°Π·Π°ΡΠ΅Π»Ρ ΠΎΠΊΠ°Π·Π°Π»ΡΡ Π² 1.4 ΡΠ°Π·Π° Π²ΡΡΠ΅, ΡΠ΅ΠΌ Π² Π³ΡΡΠΏΠΏΠ΅ ΡΡΠ°Π²Π½Π΅Π½ΠΈΡ, Π° ΠΏΡΠ» ΡΡΠ½ΠΊΡΠΈΠΎΠ½Π°Π»ΡΠ½ΠΎΠ³ΠΎ Π³Π΅ΠΌΠΎΠ³Π»ΠΎΠ±ΠΈΠ½Π° Ρ Π±ΠΎΠ»ΡΠ½ΡΡ
Π‘Π 2 ΡΠΈΠΏΠ° Π±ΡΠ» ΠΌΠ΅Π½ΡΡΠ΅, ΡΠ΅ΠΌ Ρ ΠΆΠ΅Π½ΡΠΈΠ½ Π±Π΅Π· Π‘Π.
ΠΡΠ²ΠΎΠ΄Ρ. Π£Π²Π΅Π»ΠΈΡΠ΅Π½ΠΈΠ΅ ΠΏΡΠΎΡΠ΅Π½ΡΠ½ΠΎΠ³ΠΎ ΡΠΎΠ΄Π΅ΡΠΆΠ°Π½ΠΈΡ ΠΎΡΠ½ΠΎΠ²Π½ΡΡ
ΡΡΠ°ΠΊΡΠΈΠΉ Π³Π΅ΠΌΠΎΠ³Π»ΠΎΠ±ΠΈΠ½Π° (HbAlc, Π‘ΠΠΠ¬, MetHb) ΠΏΡΠΈΠ²ΠΎΠ΄ΠΈΡ ΠΊ ΡΠ½ΠΈΠΆΠ΅Π½ΠΈΡ ΠΊΠΈΡΠ»ΠΎΡΠΎΠ΄ΡΡΠ°Π½ΡΠΏΠΎΡΡΠ½ΠΎΠΉ ΡΡΠ½ΠΊΡΠΈΠΈ Π³Π΅ΠΌΠΎΠ³Π»ΠΎΠ±ΠΈΠ½Π°. ΠΠΈΡΠ³Π΅ΠΌΠΎΠ³Π»ΠΎΠ±ΠΈΠ½Π΅ΠΌΠΈΡ Ρ ΠΏΠΎΡΠ»Π΅Π΄ΡΡΡΠ΅ΠΉ ΡΠΊΠ°Π½Π΅Π²ΠΎΠΉ Π³ΠΈΠΏΠΎΠΊΡΠΈΠ΅ΠΉ ΡΠ²Π»ΡΠ΅ΡΡΡ ΠΎΠ΄Π½ΠΈΠΌ ΠΈΠ· Π·Π²Π΅Π½ΡΠ΅Π² Π² ΠΏΠ°ΡΠΎΠ³Π΅Π½Π΅Π·Π΅ ΡΠΎΡΡΠ΄ΠΈΡΡΡΡ
Π½Π°ΡΡΡΠ΅Π½ΠΈΠΉ Ρ ΠΆΠ΅Π½ΡΠΈΠ½ Ρ Π‘Π 2 ΡΠΈΠΏΠ° Π² ΠΏΠ΅ΡΠΈΠΎΠ΄ ΠΏΠ΅ΡΠΈΠΌΠ΅Π½ΠΎΠΏΠ°ΡΠ·Ρ
Enrichment and Molecular Analysis of Breast Cancer Disseminated Tumor Cells from Bone Marrow Using Microfiltration.
PURPOSE:Molecular characterization of disseminated tumor cells (DTCs) in the bone marrow (BM) of breast cancer (BC) patients has been hindered by their rarity. To enrich for these cells using an antigen-independent methodology, we have evaluated a size-based microfiltration device in combination with several downstream biomarker assays. METHODS:BM aspirates were collected from healthy volunteers or BC patients. Healthy BM was mixed with a specified number of BC cells to calculate recovery and fold enrichment by microfiltration. Specimens were pre-filtered using a 70 ΞΌm mesh sieve and the effluent filtered through CellSieve microfilters. Captured cells were analyzed by immunocytochemistry (ICC), FISH for HER-2/neu gene amplification status, and RNA in situ hybridization (RISH). Cells eluted from the filter were used for RNA isolation and subsequent qRT-PCR analysis for DTC biomarker gene expression. RESULTS:Filtering an average of 14Γ106 nucleated BM cells yielded approximately 17-21Γ103 residual BM cells. In the BC cell spiking experiments, an average of 87% (range 84-92%) of tumor cells were recovered with approximately 170- to 400-fold enrichment. Captured BC cells from patients co-stained for cytokeratin and EpCAM, but not CD45 by ICC. RNA yields from 4 ml of patient BM after filtration averaged 135ng per 10 million BM cells filtered with an average RNA Integrity Number (RIN) of 5.3. DTC-associated gene expression was detected by both qRT-PCR and RISH in filtered spiked or BC patient specimens but, not in control filtered normal BM. CONCLUSIONS:We have tested a microfiltration technique for enrichment of BM DTCs. DTC capture efficiency was shown to range from 84.3% to 92.1% with up to 400-fold enrichment using model BC cell lines. In patients, recovered DTCs can be identified and distinguished from normal BM cells using multiple antibody-, DNA-, and RNA-based biomarker assays
2D/3D Metallic Nano-objects Self-Organized in an Organic Molecular Thin Film
We present the fabrication and investigation of the properties of nanocomposite structures consisting of two-dimensional (2D) and three-dimensional (3D) metallic nano-objects self-organized on the surface and inside of organic molecular thin-film copper tetrafluorophthalocyanine (CuPcF). Metallic atoms, deposited under ultrahigh vacuum (UHV) conditions onto the organic ultrathin film, diffuse along the surface and self-assemble into a system of 2D metallic overlayers. At the same time, the majority of the metal atoms diffuse into the organic matrix and self-organize into 3D nanoparticles (NPs) in a well-defined manner. The evolution of the morphology and electronic properties of such structures as a function of nominal metal content is studied under UHV conditions using transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HR-TEM), and photoelectron spectroscopy (PES) techniques. Using HR-TEM, we have observed the periodicity of atomic planes of individual silver NPs. The steady formation of agglomerates from individual single nanocrystallites with intercrystallite boundaries is observed as well. PES reveals generally weak chemical interactions between silver and the organic matrix and n-doping of CuPcF at the initial stages of silver deposition, which is associated with charge transfer from the 2D wetting layer on the basis of core-level spectra shift analysis
Biodiversity revision of a large arctic region as a basis for its monitoring and protection under conditions of active economic development (Nenetsky Autonomous Okrug, Russia)
In the scope of implementing a UNDP / GEF / Ministry of Nature project, a database and a GIS to consider the biodiversity of the Nenetsky Autonomous Okrug were developed. They include information on 2035 animal and 1640 plant species, belonging to 15 model groups. Data were obtained using publications and unpublished sources, the results of studying collections / herbaria of four institutes of the Russian Academy of Sciences, and data of fieldwork (2015) conducted in three coastal areas of Bolshezemelskaya Tundra. The taxonomic richness of the Nenetsky Autonomous Okrug biota is not lower (even higher in some animal groups) than in other large Arctic regions (e.g. Taymyr and Greenland). Some new vegetation syntaxa have been described. And some phytogeographic boundaries have been established. Several animal taxa have been described for the first time for science. Some of species were neither previously recorded in the Nenetsky Autonomous Okrug nor formerly known from Europe (Β«SiberianΒ» species), nor from Russia. Concerning types of ranges, the proportion of species having predominantly Siberian / East Palaearctic / Siberian-Nearctic ranges varied in different model groups from 0% to 30%. The fraction of arctic (in a wide sense) species ranged from 0% to 29%. We considered the status of the natural environment of the Nenetsky Autonomous Okrug to be satisfactory so far as its destruction is particularly local. We strongly confirm the need to create new Protected Areas. The material obtained during the project processing has been applied to the organisation of sanctuaries in the Khaipudyrskaya Bay and Pakhancheskaya Bay, Barents Sea