Artículos de revistas sobre el tema "HETEROCHIRAL PEPTIDE"
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Mortenson, David E., Jay D. Steinkruger, Dale F. Kreitler, Dominic V. Perroni, Gregory P. Sorenson, Lijun Huang, Ritesh Mittal et al. "High-resolution structures of a heterochiral coiled coil". Proceedings of the National Academy of Sciences 112, n.º 43 (12 de octubre de 2015): 13144–49. http://dx.doi.org/10.1073/pnas.1507918112.
Texto completoDemizu, Yosuke, Hiroko Yamashita, Takashi Misawa, Mitsunobu Doi, Makoto Oba, Masakazu Tanaka y Masaaki Kurihara. "Handedness Preferences of Heterochiral Helical Peptides Containing Homochiral Peptide Segments". European Journal of Organic Chemistry 2016, n.º 4 (5 de enero de 2016): 840–46. http://dx.doi.org/10.1002/ejoc.201501146.
Texto completoGoyal, Ruchika, Gaurav Jerath, Aneesh Chandrasekharan, T. R. Santhosh Kumar y Vibin Ramakrishnan. "Peptide-based delivery vectors with pre-defined geometrical locks". RSC Medicinal Chemistry 11, n.º 11 (2020): 1303–13. http://dx.doi.org/10.1039/d0md00229a.
Texto completoKovačević, Monika, Mojca Čakić Semenčić, Kristina Radošević, Krešimir Molčanov, Sunčica Roca, Lucija Šimunović, Ivan Kodrin y Lidija Barišić. "Conformational Preferences and Antiproliferative Activity of Peptidomimetics Containing Methyl 1′-Aminoferrocene-1-carboxylate and Turn-Forming Homo- and Heterochiral Pro-Ala Motifs". International Journal of Molecular Sciences 22, n.º 24 (16 de diciembre de 2021): 13532. http://dx.doi.org/10.3390/ijms222413532.
Texto completoMatsuda, Kenichi, Rui Zhai, Takahiro Mori, Masakazu Kobayashi, Ayae Sano, Ikuro Abe y Toshiyuki Wakimoto. "Heterochiral coupling in non-ribosomal peptide macrolactamization". Nature Catalysis 3, n.º 6 (4 de mayo de 2020): 507–15. http://dx.doi.org/10.1038/s41929-020-0456-7.
Texto completoPark, Hae Sook y Young Kee Kang. "Impact of aza-substitutions on the preference of helix handedness for β-peptide oligomers: a DFT study". RSC Advances 13, n.º 5 (2023): 3079–82. http://dx.doi.org/10.1039/d2ra07575j.
Texto completoAlkorta, Ibon y José Elguero. "Theoretical study of peptide model dimers. Homo versus heterochiral complexes". Journal of Molecular Structure: THEOCHEM 680, n.º 1-3 (julio de 2004): 191–98. http://dx.doi.org/10.1016/j.theochem.2004.04.030.
Texto completoXie, Yan-Yan, Xue-Qi Wang, Mei-Yan Sun, Xiao-Tong Qin, Xiao-Feng Su, Xiao-Fang Ma, Xiao-Zhi Liu, Cheng Zhong y Shi-Ru Jia. "Heterochiral peptide-based biocompatible and injectable supramolecular hydrogel with antibacterial activity". Journal of Materials Science 57, n.º 8 (febrero de 2022): 5198–209. http://dx.doi.org/10.1007/s10853-022-06982-7.
Texto completoBirch, David, Michael North, Roger R. Hill y G. E. Jeffs. "Stereochemical preference for heterochiral coupling controls selectivity in competitive peptide synthesis". Chemical Communications, n.º 10 (1999): 941–42. http://dx.doi.org/10.1039/a901730e.
Texto completoRivera Islas, Jesús, Véronique Pimienta, Jean-Claude Micheau y Thomas Buhse. "Kinetic analysis of artificial peptide self-replication. Part II: The heterochiral case". Biophysical Chemistry 103, n.º 3 (marzo de 2003): 201–11. http://dx.doi.org/10.1016/s0301-4622(02)00249-1.
Texto completoZerze, Gül H., Frank H. Stillinger y Pablo G. Debenedetti. "Effect of heterochiral inversions on the structure of a β‐hairpin peptide". Proteins: Structure, Function, and Bioinformatics 87, n.º 7 (18 de marzo de 2019): 569–78. http://dx.doi.org/10.1002/prot.25680.
Texto completoCarlomagno, Tiziano, Maria C. Cringoli, Slavko Kralj, Marina Kurbasic, Paolo Fornasiero, Paolo Pengo y Silvia Marchesan. "Biocatalysis of d,l-Peptide Nanofibrillar Hydrogel". Molecules 25, n.º 13 (30 de junio de 2020): 2995. http://dx.doi.org/10.3390/molecules25132995.
Texto completoBirch, David, Roger R. Hill, G. E. Jeffs y Michael North. "ChemInform Abstract: Stereochemical Preference for Heterochiral Coupling Controls Selectivity in Competitive Peptide Synthesis." ChemInform 30, n.º 37 (13 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199937212.
Texto completoMarchesan, S., K. E. Styan, C. D. Easton, L. Waddington y A. V. Vargiu. "Higher and lower supramolecular orders for the design of self-assembled heterochiral tripeptide hydrogel biomaterials". Journal of Materials Chemistry B 3, n.º 41 (2015): 8123–32. http://dx.doi.org/10.1039/c5tb00858a.
Texto completoKim, J. Dongun, Douglas H. Pike, Alexei M. Tyryshkin, G. V. T. Swapna, Hagai Raanan, Gaetano T. Montelione, Vikas Nanda y Paul G. Falkowski. "Minimal Heterochiral de Novo Designed 4Fe–4S Binding Peptide Capable of Robust Electron Transfer". Journal of the American Chemical Society 140, n.º 36 (24 de agosto de 2018): 11210–13. http://dx.doi.org/10.1021/jacs.8b07553.
Texto completoSaha, Indranil, Bhaswati Chatterjee, Narayanaswamy Shamala y Padmanabhan Balaram. "Crystal structures of peptide enantiomers and racemates: Probing conformational diversity in heterochiral Pro-Pro sequences". Biopolymers 90, n.º 4 (2008): 537–43. http://dx.doi.org/10.1002/bip.20982.
Texto completoSpäth, Julia, Fiona Stuart, Luyong Jiang y John A Robinson. "Stabilization of aβ-Hairpin Conformation in a Cyclic Peptide Using the Templating Effect of a Heterochiral Diproline Unit". Helvetica Chimica Acta 81, n.º 9 (9 de septiembre de 1998): 1726–38. http://dx.doi.org/10.1002/(sici)1522-2675(19980909)81:9<1726::aid-hlca1726>3.0.co;2-h.
Texto completoMakarević, Janja, Milan Jokić, Leo Frkanec, Vesna Čaplar, Nataša Šijaković Vujičić y Mladen Žinić. "Oxalyl retro-peptide gelators. Synthesis, gelation properties and stereochemical effects". Beilstein Journal of Organic Chemistry 6 (4 de octubre de 2010): 945–59. http://dx.doi.org/10.3762/bjoc.6.106.
Texto completoBhadbhade, Mohan M. y Raghuvansh Kishore. "Intramolecular CH···O Hydrogen-bond mediated stabilization of a Cis-DPro imide-bond in a stereocontrolled heterochiral model peptide". Biopolymers 97, n.º 1 (19 de agosto de 2011): 73–82. http://dx.doi.org/10.1002/bip.21705.
Texto completoNAGARAJAN, V., VASANTHA PATTABHI, A. JOHNSON, V. BOBDE y S. DURANI. "Crystal structures of heterochiral peptides". Journal of Peptide Research 49, n.º 1 (12 de enero de 2009): 74–79. http://dx.doi.org/10.1111/j.1399-3011.1997.tb01123.x.
Texto completoEGGLESTON, DRAKE S. "Heterochiral N-formyl methionyl peptides". International Journal of Peptide and Protein Research 31, n.º 2 (12 de enero de 2009): 164–72. http://dx.doi.org/10.1111/j.1399-3011.1988.tb00019.x.
Texto completoMarchesan, S., C. D. Easton, K. E. Styan, L. J. Waddington, F. Kushkaki, L. Goodall, K. M. McLean, J. S. Forsythe y P. G. Hartley. "Chirality effects at each amino acid position on tripeptide self-assembly into hydrogel biomaterials". Nanoscale 6, n.º 10 (2014): 5172–80. http://dx.doi.org/10.1039/c3nr06752a.
Texto completoGuardiola, Salvador, Monica Varese, Xavier Roig, Macarena Sánchez-Navarro, Jesús García y Ernest Giralt. "Target-templated de novo design of macrocyclic d-/l-peptides: discovery of drug-like inhibitors of PD-1". Chemical Science 12, n.º 14 (2021): 5164–70. http://dx.doi.org/10.1039/d1sc01031j.
Texto completoFlorio, Daniele, Concetta Di Natale, Pasqualina Liana Scognamiglio, Marilisa Leone, Sara La Manna, Sarah Di Somma, Paolo Antonio Netti, Anna Maria Malfitano y Daniela Marasco. "Self-assembly of bio-inspired heterochiral peptides". Bioorganic Chemistry 114 (septiembre de 2021): 105047. http://dx.doi.org/10.1016/j.bioorg.2021.105047.
Texto completoClover, Tara M., Conor L. O’Neill, Rajagopal Appavu, Giriraj Lokhande, Akhilesh K. Gaharwar, Ammon E. Posey, Mark A. White y Jai S. Rudra. "Self-Assembly of Block Heterochiral Peptides into Helical Tapes". Journal of the American Chemical Society 142, n.º 47 (27 de abril de 2020): 19809–13. http://dx.doi.org/10.1021/jacs.9b09755.
Texto completoNanda, Vikas y William F. DeGrado. "Computational Design of Heterochiral Peptides against a Helical Target". Journal of the American Chemical Society 128, n.º 3 (enero de 2006): 809–16. http://dx.doi.org/10.1021/ja054452t.
Texto completoMunegumi, Toratane y Akira Shimoyama. "Separation of homochiral peptides and heterochiral peptides in the developement of homochirality". Origins of Life and Evolution of the Biosphere 26, n.º 3-5 (octubre de 1996): 388–89. http://dx.doi.org/10.1007/bf02459827.
Texto completoChatterjee, Bhaswati, Indranil Saha, Srinivasarao Raghothama, Subrayashastry Aravinda, Rajkishor Rai, Narayanaswamy Shamala y Padmanabhan Balaram. "Designed Peptides with Homochiral and Heterochiral Diproline Templates as Conformational Constraints". Chemistry - A European Journal 14, n.º 20 (7 de julio de 2008): 6192–204. http://dx.doi.org/10.1002/chem.200702029.
Texto completoLiu, Xinyu y Samuel H. Gellman. "Comparisons of β‐Hairpin Propensity Among Peptides with Homochiral or Heterochiral Strands". ChemBioChem 22, n.º 18 (30 de julio de 2021): 2772–76. http://dx.doi.org/10.1002/cbic.202100324.
Texto completoJeena, M. T., Keunsoo Jeong, Eun Min Go, Yuri Cho, Seokyung Lee, Seongeon Jin, Suk-Won Hwang et al. "Heterochiral Assembly of Amphiphilic Peptides Inside the Mitochondria for Supramolecular Cancer Therapeutics". ACS Nano 13, n.º 10 (11 de septiembre de 2019): 11022–33. http://dx.doi.org/10.1021/acsnano.9b02522.
Texto completoBalamurugan, Dhayalan y Kannoth M. Muraleedharan. "Conformational Switching in Heterochiral α,β2,3-Hybrid Peptides in Response to Solvent Polarity". European Journal of Organic Chemistry 2015, n.º 24 (20 de julio de 2015): 5321–25. http://dx.doi.org/10.1002/ejoc.201500534.
Texto completoKantharaju, Srinivasarao Raghothama, Upadhyayula Surya Raghavender, Subrayashastry Aravinda, Narayanaswamy Shamala y Padmanabhan Balaram. "Conformations of heterochiral and homochiral proline-pseudoproline segments in peptides: Context dependentcis-transpeptide bond isomerization". Biopolymers 92, n.º 5 (2009): 405–16. http://dx.doi.org/10.1002/bip.21207.
Texto completoMunegumi, Toratane y Akira Shimoyama. "Development of homochiral peptides in the chemical evolutionary process: Separation of homochiral and heterochiral oligopeptides". Chirality 15, S1 (2003): S108—S115. http://dx.doi.org/10.1002/chir.10256.
Texto completoČakić Semenčić, Mojca, Ivan Kodrin, Lidija Barišić, Marko Nuskol y Anton Meden. "Synthesis and Conformational Study of Monosubstituted Aminoferrocene-Based Peptides Bearing Homo- and Heterochiral Pro-Ala Sequences". European Journal of Inorganic Chemistry 2017, n.º 2 (16 de agosto de 2016): 306–17. http://dx.doi.org/10.1002/ejic.201600648.
Texto completoFabiola, G. Felcy, Vivek Bobde, L. Damodharan, Vasantha Pattabhi y S. Durani. "Conformational Preferences of Heterochiral Peptides. Crystal Structures of Heterochiral Peptides Boc-(D) Val-(D) Ala-Leu-Ala-OMe and Boc-Val-Ala-Leu-(D) Ala-OMe-Enhanced Stability of β-sheet Through C-H…O Hydrogen Bonds". Journal of Biomolecular Structure and Dynamics 18, n.º 4 (1 de febrero de 2001): 579–94. http://dx.doi.org/10.1080/07391102.2001.10506690.
Texto completoFavre, Michel, Kerstin Moehle, Luyong Jiang, Bernhard Pfeiffer y John A. Robinson. "Structural Mimicry of Canonical Conformations in Antibody Hypervariable Loops Using Cyclic Peptides Containing a Heterochiral Diproline Template". Journal of the American Chemical Society 121, n.º 12 (marzo de 1999): 2679–85. http://dx.doi.org/10.1021/ja984016p.
Texto completoLee, Hye-soo y Yong-beom Lim. "Slow-Motion Self-Assembly: Access to Intermediates with Heterochiral Peptides to Gain Control over Alignment Media Development". ACS Nano 14, n.º 3 (14 de febrero de 2020): 3344–52. http://dx.doi.org/10.1021/acsnano.9b09070.
Texto completoDemizu, Yosuke, Hiroko Yamashita, Mitsunobu Doi, Takashi Misawa, Makoto Oba, Masakazu Tanaka y Masaaki Kurihara. "Topological Study of the Structures of Heterochiral Peptides Containing Equal Amounts of l-Leu and d-Leu". Journal of Organic Chemistry 80, n.º 17 (22 de agosto de 2015): 8597–603. http://dx.doi.org/10.1021/acs.joc.5b01541.
Texto completoKamada, Rui, Natsumi Nakagawa, Taiji Oyama y Kazuyasu Sakaguchi. "Heterochiral Jun and Fos bZIP peptides form a coiled-coil heterodimer that is competent for DNA binding". Journal of Peptide Science 23, n.º 7-8 (10 de febrero de 2017): 644–49. http://dx.doi.org/10.1002/psc.2985.
Texto completoUdagawa, Hinako, Takato H. Yoneda, Ryo Masuda y Takaki Koide. "A Strategy for Discovering Heterochiral Bioactive Peptides by Using the OB2 n P Library and SPOTs Method". ChemBioChem 20, n.º 16 (15 de julio de 2019): 2070–73. http://dx.doi.org/10.1002/cbic.201900237.
Texto completoZhou, Yu, Chris Oostenbrink, Wilfred F. Van Gunsteren, Wilfred R. Hagen, Simon W. De Leeuw y Jaap A. Jongejan *. "Relative stability of homochiral and heterochiral dialanine peptides. Effects of perturbation pathways and force-field parameters on free energy calculations". Molecular Physics 103, n.º 14 (20 de julio de 2005): 1961–69. http://dx.doi.org/10.1080/00268970500096889.
Texto completoDi Blasio, Benedetto, Michele Saviano, Valerio Del Duca, Giuseppina De Simone, Filomena Rossi, Carlo Pedone, Ettore Benedetti y Gian Paolo Lorenzi. "Conformational studies of heterochiral peptides with diastereoisomeric residues: Crystal and molecular structures of linear dipeptides derived from leucine, isoleucine, and allo-isoleucine". Biopolymers 36, n.º 4 (octubre de 1995): 401–8. http://dx.doi.org/10.1002/bip.360360403.
Texto completoRao, I. Nageshwara, Anima Boruah, S. Kiran Kumar, A. C. Kunwar, A. Sivalakshmi Devi, K. Vyas, Krishnan Ravikumar y Javed Iqbal. "Synthesis and Conformational Studies of Novel Cyclic Peptides Constrained into a 310Helical Structure by a Heterochirald-Pro-l-Pro Dipeptide Template". Journal of Organic Chemistry 69, n.º 6 (marzo de 2004): 2181–84. http://dx.doi.org/10.1021/jo030282w.
Texto completoZhou, Yu, Chris Oostenbrink, Aldo Jongejan, Wilfred F. Van Gunsteren, Wilfred R. Hagen, Simon W. De Leeuw y Jaap A. Jongejan. "Computational study of ground-state chiral induction in small peptides: Comparison of the relative stability of selected amino acid dimers and oligomers in homochiral and heterochiral combinations". Journal of Computational Chemistry 27, n.º 7 (2006): 857–67. http://dx.doi.org/10.1002/jcc.20378.
Texto completoShao, Ning, Ling Yuan, Pengcheng Ma, Min Zhou, Ximian Xiao, Zihao Cong, Yueming Wu, Guohui Xiao, Jian Fei y Runhui Liu. "Heterochiral β-Peptide Polymers Combating Multidrug-Resistant Cancers Effectively without Inducing Drug Resistance". Journal of the American Chemical Society, 14 de abril de 2022. http://dx.doi.org/10.1021/jacs.2c00452.
Texto completoRai, Rishika y Kana M. Sureshan. "Topochemical Synthesis of a Heterochiral Peptide Polymer in Different Polymorphic Forms from Crystals and Aerogels". Angewandte Chemie International Edition 61, n.º 16 (23 de febrero de 2022). http://dx.doi.org/10.1002/anie.202111623.
Texto completoRai, Rishika y Kana M. Sureshan. "Topochemical Synthesis of a Heterochiral Peptide Polymer in Different Polymorphic Forms from Crystals and Aerogels". Angewandte Chemie 134, n.º 16 (23 de febrero de 2022). http://dx.doi.org/10.1002/ange.202111623.
Texto completoRahman, Md Wazedur, Mari C. Mañas-Torres, Seyedamin Firouzeh, Sara Illescas-Lopez, Juan Manuel Cuerva, Modesto T. Lopez-Lopez, Luis Álvarez de Cienfuegos y Sandipan Pramanik. "Chirality-Induced Spin Selectivity in Heterochiral Short-Peptide–Carbon-Nanotube Hybrid Networks: Role of Supramolecular Chirality". ACS Nano, 11 de octubre de 2022. http://dx.doi.org/10.1021/acsnano.2c07040.
Texto completoTeng, Peng, Mengmeng Zheng, Darrell Cole Cerrato, Yan Shi, Mi Zhou, Songyi Xue, Wei Jiang et al. "The folding propensity of α/sulfono-γ-AA peptidic foldamers with both left- and right-handedness". Communications Chemistry 4, n.º 1 (10 de mayo de 2021). http://dx.doi.org/10.1038/s42004-021-00496-0.
Texto completoYang, Xuejiao, Honglei Lu, Yinghua Tao, Hongyue Zhang y Huaimin Wang. "Controlling supramolecular filament chirality of hydrogel by co-assembly of enantiomeric aromatic peptides". Journal of Nanobiotechnology 20, n.º 1 (10 de febrero de 2022). http://dx.doi.org/10.1186/s12951-022-01285-0.
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