Arundhati Nag

发表

Protein-targeting strategy used to develop a selective inhibitor of the E17K point mutation in the PH Domain of Akt1

J. Heath, B. Lai, K. Deyle, 2015, Nature chemistry.

A General Synthetic Approach for Designing Epitope Targeted Macrocyclic Peptide Ligands.

Amethist S. Finch, Matthew B. Coppock, Deborah A. Sarkes, 2015, Angewandte Chemie.

Copper–ligand clusters dictate size of cyclized peptide formed during alkyne–azide cycloaddition on solid support

Arundhati Nag, S. Das, René Kandler, 2021, RSC advances.

Degradation of Akt using protein‐catalyzed capture agents

A. Sutherland, J. Varghese, Arundhati Nag, 2016, Journal of peptide science : an official publication of the European Peptide Society.

Iterative in situ click chemistry creates antibody-like protein-capture agents.

Jason E Hein, Arundhati Nag, James R Heath, 2009, Angewandte Chemie.

Iterative in situ click chemistry assembles a branched capture agent and allosteric inhibitor for Akt1.

J. Heath, Su Seong Lee, K. Sharpless, 2011, Journal of the American Chemical Society.

Epitope targeting of tertiary protein structure enables target-guided synthesis of a potent in-cell inhibitor of botulinum neurotoxin.

J. Heath, Heather D Agnew, B. Lai, 2015, Angewandte Chemie.

A chemical epitope-targeting strategy for protein capture agents: the serine 474 epitope of the kinase Akt2.

J. Heath, K. Deyle, S. Millward, 2013, Angewandte Chemie.

In situ click chemistry: from small molecule discovery to synthetic antibodies.

J. Heath, Su Seong Lee, Jaehong Lim, 2013, Integrative biology : quantitative biosciences from nano to macro.

Corrigendum: Epitope Targeting of Tertiary Protein Structure Enables Target-Guided Synthesis of a Potent In-Cell Inhibitor of Botulinum Neurotoxin.

J. Heath, Heather D Agnew, B. Lai, 2018, Angewandte Chemie.

Biological applications of amide and amino acid containing synthetic macrocycles

Arundhati Nag, A. Borges, D. Gillespie, 2019, Supramolecular Chemistry.

Fluorescent Sensors of Phosphate Containing Biomolecules

Arundhati Nag, S. Das, 2020 .

Stereochemical engineering yields a multifunctional peptide macrocycle inhibitor of Akt2 by fine-tuning macrocycle-cell membrane interactions

Samir R Das, W. Goddard, Yapeng Su, 2023, Communications chemistry.

Stereochemical engineering of a peptide macrocycle allosteric inhibitor of phospho-Akt2 controls cell penetration by fine-tuning macrocycle-cell membrane interactions

Samir R Das, W. Goddard, A. Mafi, 2021 .

Facile de Novo Sequencing of Tetrazine‐Cyclized Peptides through UV‐Induced Ring‐Opening and Cleavage from the Solid Phase

Samir R Das, Arundhati Nag, René Kandler, 2022, Chembiochem : a European journal of chemical biology.

Iterative in situ click chemistry assembles a branched capture agent and allosteric inhibitor for Akt1.

Su Seong Lee, K. Sharpless, Jaehong Lim, 2011, Journal of the American Chemical Society.

Chemical Epitope Targeting: Review of a Novel Screening Technology

Arundhati Nag, René Kandler, Qurrat ul-Ain, 2018 .

A Copper-Selective Sensor and Its Inhibition of Copper-Amyloid Beta Aggregation

Arundhati Nag, Ngoc Kim Nguyen, Bella Poduska, 2024, Biosensors.

Binding Characterization of Cyclic Peptide Ligands to Target Proteins and Chemical Epitopes Using ELISA and Fluorescence Polarization Assays.

Arundhati Nag, A. Borges, Iryna Onasenko, 2021, Methods in molecular biology.