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Journal articles on the topic 'Tribranched'

Author: Grafiati

Published: 9 March 2023

Last updated: 10 March 2023

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1

He, Guiying, Jinjun Shao, Yang Li, Jiangpu Hu, Huaning Zhu, Xian Wang, Qianjin Guo, Chunyan Chi, and Andong Xia. "Photophysical properties of octupolar triazatruxene-based chromophores." Physical Chemistry Chemical Physics 18, no. 9 (2016): 6789–98. http://dx.doi.org/10.1039/c5cp07563g.

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2

Suzuki, Akira, Munetaka Akita, and Michito Yoshizawa. "Amphiphilic tribranched scaffolds with polyaromatic panels that wrap perylene stacks displaying unusual emissions." Chemical Communications 52, no. 65 (2016): 10024–27. http://dx.doi.org/10.1039/c6cc04823d.

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A spherical assembly containing a perylene stack, prepared from a rigid tribranched scaffold and perylene, exhibits unusual Y-emission in water at room temperature. In contrast, an analogous assembly from a flexible scaffold and perylene shows E-emission under the same conditions.

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3

Zhang, Ji-Na, Hong Li, Wei Zhou, Shi-Lin Yu, Da-Hui Qu, and He Tian. "Fluorescence Modulation in Tribranched Switchable [4]Rotaxanes." Chemistry - A European Journal 19, no. 50 (November 7, 2013): 17192–200. http://dx.doi.org/10.1002/chem.201303026.

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4

Tateishi-Karimata, Hisae, Tatsuya Ohyama, Takahiro Muraoka, Shigenori Tanaka, Kazushi Kinbara, and Naoki Sugimoto. "New Modified Deoxythymine with Dibranched Tetraethylene Glycol Stabilizes G-Quadruplex Structures." Molecules 25, no. 3 (February 6, 2020): 705. http://dx.doi.org/10.3390/molecules25030705.

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Methods for stabilizing G-quadruplex formation is a promising therapeutic approach for cancer treatment and other biomedical applications because stable G-quadruplexes efficiently inhibit biological reactions. Oligo and polyethylene glycols are promising biocompatible compounds, and we have shown that linear oligoethylene glycols can stabilize G-quadruplexes. Here, we developed a new modified deoxythymine with dibranched or tribranched tetraethylene glycol (TEG) and incorporated these TEG-modified deoxythymines into a loop region that forms an antiparallel G-quadruplex. We analyzed the stability of the modified G-quadruplexes, and the results showed that the tribranched TEG destabilized G-quadruplexes through entropic contributions, likely through steric hindrance. Interestingly, the dibranched TEG modification increased G-quadruplex stability relative to the unmodified DNA structures due to favorable enthalpic contributions. Molecular dynamics calculations suggested that dibranched TEG interacts with the G-quadruplex through hydrogen bonding and CH-π interactions. Moreover, these branched TEG-modified deoxythymine protected the DNA oligonucleotides from degradation by various nucleases in human serum. By taking advantage of the unique interactions between DNA and branched TEG, advanced DNA materials can be developed that affect the regulation of DNA structure.

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5

VALLE, Cristina. "On the blow-analytic equivalence of tribranched plane curves." Journal of the Mathematical Society of Japan 68, no. 2 (April 2016): 823–38. http://dx.doi.org/10.2969/jmsj/06820823.

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6

Friedl, Stefan, Takahiro Kitayama, and Matthias Nagel. "A note on the existence of essential tribranched surfaces." Topology and its Applications 225 (July 2017): 75–82. http://dx.doi.org/10.1016/j.topol.2017.04.023.

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7

Lee, Geon Hyeong, and Young Sik Kim. "Theoretical study of tribranched organic sensitizer for Efficient Dye-sensitized solar cells." Molecular Crystals and Liquid Crystals 653, no. 1 (August 13, 2017): 260–66. http://dx.doi.org/10.1080/15421406.2017.1354654.

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8

Zhu, Lin, Wen Lv, Shujuan Liu, Hong Yan, Qiang Zhao, and Wei Huang. "Carborane enhanced two-photon absorption of tribranched fluorophores for fluorescence microscopy imaging." Chemical Communications 49, no. 90 (2013): 10638. http://dx.doi.org/10.1039/c3cc46276e.

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9

Abbotto, Alessandro, Valentina Leandri, Norberto Manfredi, Filippo De Angelis, Mariachiara Pastore, Jun-Ho Yum, Mohammad K. Nazeeruddin, and Michael Grätzel. "Bis-Donor-Bis-Acceptor Tribranched Organic Sensitizers for Dye-Sensitized Solar Cells." European Journal of Organic Chemistry 2011, no. 31 (September 5, 2011): 6195–205. http://dx.doi.org/10.1002/ejoc.201100821.

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10

Leandri, Valentina, Riccardo Ruffo, Vanira Trifiletti, and Alessandro Abbotto. "Asymmetric Tribranched Dyes: An Intramolecular Cosensitization Approach for Dye-Sensitized Solar Cells." European Journal of Organic Chemistry 2013, no. 30 (August 20, 2013): 6793–801. http://dx.doi.org/10.1002/ejoc.201300962.

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11

Hu, Jiangpu, Yang Li, Huaning Zhu, Shuhai Qiu, Guiying He, Xiaozhang Zhu, and Andong Xia. "Photophysical Properties of Intramolecular Charge Transfer in a Tribranched Donor-π-Acceptor Chromophore." ChemPhysChem 16, no. 11 (May 28, 2015): 2357–65. http://dx.doi.org/10.1002/cphc.201500290.

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12

Lee, Geon Hyeong, and Young Sik Kim. "Effect of Tribranched Organic Dyes with Heteroleptic Dual Acceptor for Dye-Sensitized Solar Cells." Journal of Nanoscience and Nanotechnology 17, no. 11 (November 1, 2017): 8383–88. http://dx.doi.org/10.1166/jnn.2017.15139.

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13

Li, Bo, Rui Tong, Rongyi Zhu, Fanshun Meng, He Tian, and Shixiong Qian. "The Ultrafast Dynamics and Nonlinear Optical Properties of Tribranched Styryl Derivatives Based on 1,3,5-Triazine." Journal of Physical Chemistry B 109, no. 21 (June 2005): 10705–10. http://dx.doi.org/10.1021/jp050368o.

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14

Jia, Mingli, Xiaonan Ma, Linyin Yan, Haifeng Wang, Qianjin Guo, Xuefei Wang, Yingying Wang, Xiaowei Zhan, and Andong Xia. "Photophysical Properties of Intramolecular Charge Transfer in Two Newly Synthesized Tribranched Donor−π−Acceptor Chromophores." Journal of Physical Chemistry A 114, no. 27 (July 15, 2010): 7345–52. http://dx.doi.org/10.1021/jp1032355.

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15

Li, Bo, Rui Tong, Rongyi Zhu, Jianli Hua, He Tian, and Shixiong Qian. "The ultrafast dynamics and nonlinear optical properties of tribranched conjugated polymers with triphenylamine as the core." Journal of Luminescence 119-120 (July 2006): 116–21. http://dx.doi.org/10.1016/j.jlumin.2005.12.019.

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16

Peyfoon, Elham, Benjamin Meyer, Paul G. Hitchen, Maria Panico, Howard R. Morris, Stuart M. Haslam, Sonja-Verena Albers, and Anne Dell. "The S-Layer Glycoprotein of the CrenarchaeoteSulfolobus acidocaldariusIs Glycosylated at Multiple Sites with Chitobiose-LinkedN-Glycans." Archaea 2010 (2010): 1–10. http://dx.doi.org/10.1155/2010/754101.

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Glycosylation of the S-layer of the crenarchaeaSulfolobus acidocaldariushas been investigated using glycoproteomic methodologies. The mature protein is predicted to contain 31 N-glycosylation consensus sites with approximately one third being found in the C-terminal domain spanning residuesL1004-Q1395. Since this domain is rich in Lys and Arg and therefore relatively tractable to glycoproteomic analysis, this study has focused on mapping its N-glycosylation. Our analysis identified nine of the 11 consensus sequence sites, and all were found to be glycosylated. This constitutes a remarkably high glycosylation density in the C-terminal domain averaging one site for each stretch of 30–40 residues. Each of the glycosylation sites observed was shown to be modified with a heterogeneous family of glycans, with the largest having a composition Glc1Man2GlcNAc2plus 6-sulfoquinovose (QuiS), consistent with the tribranched hexasaccharide previously reported in the cytochromeb558/566ofS. acidocaldarius.S. acidocaldariusis the only archaeal species whose N-glycans are known to be linked via the chitobiose core disaccharide that characterises the N-linked glycans ofEukarya.

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17

Santhosh, N. S., and G. Sundararajan. "Novel Linear and Tribranched Polymers with Redox-Active End Groups via W(CO)6-Initiated Metathesis Polymerization." Organic Letters 8, no. 4 (February 2006): 605–8. http://dx.doi.org/10.1021/ol052774w.

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18

Liu, Li, Wei Huang, Jieping Shi, Changgui Lü, Yiping Cui, and Guo-Yuan Lu. "Synthesis, Photophysical Properties of Tribranched Chromophores Based on 1,3,5-Triazine Core and Different Electro-donating End-groups." Chinese Journal of Chemistry 29, no. 10 (October 2011): 2129–33. http://dx.doi.org/10.1002/cjoc.201180369.

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19

Leandri, Valentina, Riccardo Ruffo, Vanira Trifiletti, and Alessandro Abbotto. "Asymmetric Tribranched Dyes: An Intramolecular Cosensitization Approach for Dye-Sensitized Solar Cells (Eur. J. Org. Chem. 30/2013)." European Journal of Organic Chemistry 2013, no. 30 (October 2013): n/a. http://dx.doi.org/10.1002/ejoc.201390085.

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20

Liu, Li, Zhiqiang Zhou, Jieping Shi, Zeyu Liu, Changgui Lu, Weijiang He, Jing Ma, Yiping Cui, and Guo-Yuan Lu. "Photophysical and two-photon absorption properties of protonation-induced tribranched chromophore having 1,3,5-triazine core and pyrrole end-groups." Synthetic Metals 161, no. 9-10 (May 2011): 783–88. http://dx.doi.org/10.1016/j.synthmet.2011.01.030.

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21

Liu, Li, Wei Huang, Jieping Shi, Changgui Lue, Yiping Cui, and Guo-Yuan Lu. "ChemInform Abstract: Synthesis, Photophysical Properties of Tribranched Chromophores Based on 1,3,5-Triazine Core and Different Electro-Donating Eng-Groups." ChemInform 43, no. 8 (January 27, 2012): no. http://dx.doi.org/10.1002/chin.201208203.

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22

Lee, Geon Hyeong, and Young Sik Kim. "Theoretical study of an asymmetric A-π-D-π-D-π-A′ tribranched organic sensitizer for dye-sensitized solar cells." Journal of the Korean Physical Society 69, no. 3 (August 2016): 381–85. http://dx.doi.org/10.3938/jkps.69.381.

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23

Ikeda, Taichi. "Poly(ionic liquid)s Based on Copolymers of Poly(ethylene oxide) and Cationic Glycidyl Triazolyl Polymers with Tribranched Side Chains." ACS Macro Letters 10, no. 7 (June 18, 2021): 831–36. http://dx.doi.org/10.1021/acsmacrolett.1c00253.

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24

Lee, Kyung-Hoon, Jun-Woo Lee, and Jung-Il Jin. "Liquid crystalline compounds having a tribranched structure: substituted malonic esters consisting of two Schiff's base units and a cholesteryloxyalkyl substituent." Liquid Crystals 28, no. 10 (October 2001): 1519–25. http://dx.doi.org/10.1080/02678290110071547.

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25

Fakis, M., I. Fitilis, S. Stefanatos, P. Vellis, J. Mikroyannidis, V. Giannetas, and P. Persephonis. "The photophysics and two-photon absorption of a series of quadrupolar and tribranched molecules: The role of the edge substituent." Dyes and Pigments 81, no. 1 (April 2009): 63–68. http://dx.doi.org/10.1016/j.dyepig.2008.08.014.

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26

Rao, Xianhua, Guodong Dang, Hongwei Zhou, Wei Yang, Gang Cui, Chunhai Chen, and Rikio Yokota. "Design and synthesis of a tribranched phenylethynyl-terminated aryl ether compound and its use as a reactive diluent for PETI-5." Journal of Polymer Science Part A: Polymer Chemistry 45, no. 21 (September 14, 2007): 4844–54. http://dx.doi.org/10.1002/pola.22223.

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27

Lin, Jung-Fong, Ching-Fu Ho, and Steve K. Huang. "Studies on curing kinetics and total thermal degradation of the modified epoxy copolymer with penta-coordinated phosphate as a tribranched junction." Journal of Applied Polymer Science 77, no. 4 (July 25, 2000): 719–32. http://dx.doi.org/10.1002/(sici)1097-4628(20000725)77:4<719::aid-app2>3.0.co;2-7.

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28

Xiang, Yong, Khanita Karaveg, and Kelley W. Moremen. "Substrate recognition and catalysis by GH47 α-mannosidases involved in Asn-linked glycan maturation in the mammalian secretory pathway." Proceedings of the National Academy of Sciences 113, no. 49 (November 17, 2016): E7890—E7899. http://dx.doi.org/10.1073/pnas.1611213113.

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Maturation of Asn-linked oligosaccharides in the eukaryotic secretory pathway requires the trimming of nascent glycan chains to remove all glucose and several mannose residues before extension into complex-type structures on the cell surface and secreted glycoproteins. Multiple glycoside hydrolase family 47 (GH47) α-mannosidases, including endoplasmic reticulum (ER) α-mannosidase I (ERManI) and Golgi α-mannosidase IA (GMIA), are responsible for cleavage of terminal α1,2-linked mannose residues to produce uniquely trimmed oligomannose isomers that are necessary for ER glycoprotein quality control and glycan maturation. ERManI and GMIA have similar catalytic domain structures, but each enzyme cleaves distinct residues from tribranched oligomannose glycan substrates. The structural basis for branch-specific cleavage by ERManI and GMIA was explored by replacing an essential enzyme-bound Ca2+ ion with a lanthanum (La3+) ion. This ion swap led to enzyme inactivation while retaining high-affinity substrate interactions. Cocrystallization of La3+-bound enzymes with Man9GlcNAc2 substrate analogs revealed enzyme–substrate complexes with distinct modes of glycan branch insertion into the respective enzyme active-site clefts. Both enzymes had glycan interactions that extended across the entire glycan structure, but each enzyme engaged a different glycan branch and used different sets of glycan interactions. Additional mutagenesis and time-course studies of glycan cleavage probed the structural basis of enzyme specificity. The results provide insights into the enzyme catalytic mechanisms and reveal structural snapshots of the sequential glycan cleavage events. The data also indicate that full steric access to glycan substrates determines the efficiency of mannose-trimming reactions that control the conversion to complex-type structures in mammalian cells.

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29

BIAN, XUN, FU-MING SHI, and YAN-LIN CHANG. "Review of the genus Phlugiolopsis Zeuner, 1940 (Orthoptera: Tettigoniidae: Meconematinae) from China." Zootaxa 3281, no. 1 (April 27, 2012): 1. http://dx.doi.org/10.11646/zootaxa.3281.1.1.

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This paper reviews the genus Phlugiolopsis Zeuner, 1940, and describes 5 new species from China, Phlugiolopsis pectinissp. nov., Phlugiolopsis tribranchis sp. nov., Phlugiolopsis digitusis sp. nov., Phlugiolopsis trullis sp. nov. andPhlugiolopsis adentis sp. nov. A key to the species and distributional data in China are given. The type specimens are deposited in the Museum of Hebei University.

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30

Gorochov, A. V. "New species of the genus Phlugiolopsis from its subgenus Omkoiana stat. nov. (Orthoptera: Tettigoniidae: Meconematinae)." Proceedings of the Zoological Institute RAS 324, no. 3 (September 25, 2020): 346–52. http://dx.doi.org/10.31610/trudyzin/2020.324.3.346.

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The genus Phlugiolopsis Zeuner, 1940 is considered: its brief comparison with some similar genera is given, and its subgeneric composition is discussed. This genus is tentatively subdivided into two subgenera: Phlugiolopsis s. str. with three possible species; the subgenus Omkoiana Sänger et Helfert, 2002, stat. nov. with all the other species of this genus including three “subgenera” with unclear status (Longiloba Bian et Shi, 2018; Tribranchis Bian et Shi, 2018; Uncinata Bian et Shi, 2018). Two new species, Ph. (O.) trilobulata sp. nov. with three lobes on the male cercus and Ph. (O.) bilobulata sp. nov. with two such lobes, are described from Vietnam and Indonesia, respectively; these species additionally differ from each other in the male genital plate with specialized apical hooks (Ph. trilobulata sp. nov.) or with a slightly bilobate apex (Ph. bilobulata sp. nov.). From the other congeners, these species are distinguished by the same characters as well as some other features connected mainly with shape of the male cercal lobes and of the female genital plate.

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31

Hussein, Essam M., Nizar El Guesmi, and Saleh A. Ahmed. "Distinctive tunable photophysical properties of versatile environmentally-sensitive tribranched cyanopyridine fluorophores." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, November 2020, 119169. http://dx.doi.org/10.1016/j.saa.2020.119169.

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32

Liu, Li, Zhi Qiang Zhou, Jie Ping Shi, Chang Gui Lu, Yi Ping Cui, and Guo Yuan Lu. "Synthesis and properties of tribranched chromophores with triazine and fluorene units." Chinese Chemical Letters, July 2011. http://dx.doi.org/10.1016/j.cclet.2011.05.045.

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33

"2012 TriBranch Symposium." Lab Animal 41, no. 8 (July 20, 2012): 215. http://dx.doi.org/10.1038/laban0812-215.

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34

"2013 Tribranch Symposium." Lab Animal 42, no. 8 (July 22, 2013): 275. http://dx.doi.org/10.1038/laban.354.

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