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Arundhati Nag, Ph.D. - Publications

Affiliations: 
2013 Chemistry California Institute of Technology, Pasadena, CA 
Area:
solid-state quantum physics, materials science, basic surface science, Microfluidics-based assays of blood proteins, artificial antibodies
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16 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Das S, Nag A. Tetrazine cyclized peptides for one-bead-one-compound library: Synthesis and sequencing. Methods in Enzymology. 698: 141-167. PMID 38886030 DOI: 10.1016/bs.mie.2024.04.015  0.469
2023 Nag A, Mafi A, Das S, Yu MB, Alvarez-Villalonga B, Kim SK, Su Y, Goddard WA, Heath JR. Stereochemical engineering yields a multifunctional peptide macrocycle inhibitor of Akt2 by fine-tuning macrocycle-cell membrane interactions. Communications Chemistry. 6: 95. PMID 37202473 DOI: 10.1038/s42004-023-00890-w  0.808
2022 Borges A, Nguyen C, Letendre M, Onasenko I, Kandler R, Nguyen NK, Chen J, Allakhverdova T, Atkinson E, DiChiara B, Wang C, Petler N, Patel H, Nanavati D, Das S, ... Nag A, et al. Facile de novo sequencing of tetrazine-cyclized peptides through UV-induced ring-opening and cleavage from solid phase. Chembiochem : a European Journal of Chemical Biology. PMID 36471561 DOI: 10.1002/cbic.202200590  0.425
2022 Borges A, Onasenko I, Nag A. Binding Characterization of Cyclic PeptideĀ Ligands to Target Proteins and Chemical Epitopes Using ELISA and Fluorescence Polarization Assays. Methods in Molecular Biology (Clifton, N.J.). 2371: 335-354. PMID 34596857 DOI: 10.1007/978-1-0716-1689-5_18  0.516
2021 Kandler R, Das S, Nag A. Copper-ligand clusters dictate size of cyclized peptide formed during alkyne-azide cycloaddition on solid support. Rsc Advances. 11: 4842-4852. PMID 34377440 DOI: 10.1039/D0RA07491H  0.458
2018 Farrow B, Wong M, Malette J, Lai B, Deyle KM, Das S, Nag A, Agnew HD, Heath JR. Corrigendum: Epitope Targeting of Tertiary Protein Structure Enables Target-Guided Synthesis of a Potent In-Cell Inhibitor of Botulinum Neurotoxin. Angewandte Chemie (International Ed. in English). 57: 1439. PMID 29377421 DOI: 10.1002/anie.201712967  0.771
2016 Henning RK, Varghese JO, Das S, Nag A, Tang G, Tang K, Sutherland AM, Heath JR. Degradation of Akt using protein-catalyzed capture agents. Journal of Peptide Science : An Official Publication of the European Peptide Society. PMID 26880702 DOI: 10.1002/Psc.2858  0.681
2016 Nag A. Abstract 2172: Circle Akt in: Epitope catalyzed assembly of macrocyclic therapeutics against phosphorylated Akt Cancer Research. 76: 2172-2172. DOI: 10.1158/1538-7445.Am2016-2172  0.658
2016 Liang J, Nag A, Das S, Bunck D, McCarthy A, Mishra A, Heath JE, Villalonga B, Heath JR. Detection of a Geographically Diverse Malarial Biomarker via Multi-Epitope Targeted Screening Biophysical Journal. 110: 519a. DOI: 10.1016/J.Bpj.2015.11.2774  0.799
2015 Das S, Nag A, Liang J, Bunck DN, Umeda A, Farrow B, Coppock MB, Sarkes DA, Finch AS, Agnew HD, Pitram S, Lai B, Yu MB, Museth AK, Deyle KM, et al. A General Synthetic Approach for Designing Epitope Targeted Macrocyclic Peptide Ligands. Angewandte Chemie (International Ed. in English). PMID 26377818 DOI: 10.1002/Anie.201505243  0.714
2015 Farrow B, Wong M, Malette J, Lai B, Deyle KM, Das S, Nag A, Agnew HD, Heath JR. Epitope targeting of tertiary protein structure enables target-guided synthesis of a potent in-cell inhibitor of botulinum neurotoxin. Angewandte Chemie (International Ed. in English). 54: 7114-9. PMID 25925721 DOI: 10.1002/Anie.201502451  0.801
2015 Deyle KM, Farrow B, Qiao Hee Y, Work J, Wong M, Lai B, Umeda A, Millward SW, Nag A, Das S, Heath JR. A protein-targeting strategy used to develop a selective inhibitor of the E17K point mutation in the PH domain of Akt1. Nature Chemistry. 7: 455-62. PMID 25901825 DOI: 10.1038/Nchem.2223  0.789
2013 Nag A, Das S, Yu MB, Deyle KM, Millward SW, Heath JR. A chemical epitope-targeting strategy for protein capture agents: the serine 474 epitope of the kinase Akt2. Angewandte Chemie (International Ed. in English). 52: 13975-9. PMID 24254999 DOI: 10.1002/Anie.201305882  0.837
2013 Millward SW, Agnew HD, Lai B, Lee SS, Lim J, Nag A, Pitram S, Rohde R, Heath JR. In situ click chemistry: from small molecule discovery to synthetic antibodies. Integrative Biology : Quantitative Biosciences From Nano to Macro. 5: 87-95. PMID 22836343 DOI: 10.1039/C2Ib20110K  0.85
2011 Millward SW, Henning RK, Kwong GA, Pitram S, Agnew HD, Deyle KM, Nag A, Hein J, Lee SS, Lim J, Pfeilsticker JA, Sharpless KB, Heath JR. Iterative in situ click chemistry assembles a branched capture agent and allosteric inhibitor for Akt1. Journal of the American Chemical Society. 133: 18280-8. PMID 21962254 DOI: 10.1021/Ja2064389  0.755
2009 Agnew HD, Rohde RD, Millward SW, Nag A, Yeo WS, Hein JE, Pitram SM, Tariq AA, Burns VM, Krom RJ, Fokin VV, Sharpless KB, Heath JR. Iterative in situ click chemistry creates antibody-like protein-capture agents. Angewandte Chemie (International Ed. in English). 48: 4944-8. PMID 19301344 DOI: 10.1002/Anie.200900488  0.814
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