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Epitope Discovery for a Synthetic Polymer Nanoparticle: A New Strategy for Developing a Peptide Tag

Journal of the American Chemical Society, 2014-01, Vol.136 (4), p.1194-1197

2014

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Utilization of tyrosine- and histidine-containing dipeptides to enhance productivity and culture viability

Biotechnology and bioengineering, 2012-09, Vol.109 (9), p.2286-2294

2012

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Development of human-machine language interfaces for the visual analysis of complex biologics and RNA modalities and associated experimental data

AAPS open, 2023-03, Vol.9 (1), p.5-11, Article 5

2023

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Identification of Antibody and Small Molecule Antagonists of Ferroportin-Hepcidin Interaction

Frontiers in pharmacology, 2017-11, Vol.8, p.838-838

2017

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Structure-guided Discovery of Dual-recognition Chemibodies

Scientific reports, 2018-05, Vol.8 (1), p.7570-9, Article 7570

2018

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Engineering Potent and Selective Analogues of GpTx-1, a Tarantula Venom Peptide Antagonist of the NaV1.7 Sodium Channel

Journal of medicinal chemistry, 2015-03, Vol.58 (5), p.2299-2314

2015

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Accelerating attribute‐focused process and product development through the development and deployment of autonomous process analytical technology platform system

Biotechnology and bioengineering, 2024-04, Vol.121 (4), p.1257-1270

2024

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Process development of a SARS-CoV-2 nanoparticle vaccine

Process biochemistry (1991), 2023-06, Vol.129, p.241-256

2023

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Metal-Free Polymer-Based Affinity Medium for Selective Purification of His6-Tagged Proteins

Biomacromolecules, 2021-04, Vol.22 (4), p.1695-1705

2021

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Discovery of Tarantula Venom-Derived NaV1.7-Inhibitory JzTx‑V Peptide 5‑Br-Trp24 Analogue AM-6120 with Systemic Block of Histamine-Induced Pruritis

Journal of medicinal chemistry, 2018-11, Vol.61 (21), p.9500-9512

2018

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Half-life extension of peptidic APJ agonists by N-terminal lipid conjugation

Bioorganic & medicinal chemistry letters, 2020-11, Vol.30 (21), p.127499-127499, Article 127499

2020

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Accelerated Chemical Synthesis of Peptides and Small Proteins

Proceedings of the National Academy of Sciences - PNAS, 1999-02, Vol.96 (4), p.1181-1186

1999

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Use of Cryopreserved Hepatocytes as Part of an Integrated Strategy to Characterize In Vivo Clearance for Peptide-Antibody Conjugate Inhibitors of Nav1.7 in Preclinical Species

Drug metabolism and disposition, 2019-10, Vol.47 (10), p.1111-1121

2019

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Discovery of Tarantula Venom-Derived Na V 1.7-Inhibitory JzTx-V Peptide 5-Br-Trp24 Analogue AM-6120 with Systemic Block of Histamine-Induced Pruritis

Journal of medicinal chemistry, 2018-11, Vol.61 (21), p.9500-9512

2018

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Engineering Antibody Reactivity for Efficient Derivatization to Generate NaV1.7 Inhibitory GpTx‑1 Peptide–Antibody Conjugates

ACS chemical biology, 2017-09, Vol.12 (9), p.2427-2435

2017

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Fmoc-Protein Synthesis: Preparation of Peptide Thioesters Using a Side-Chain Anchoring Strategy

International journal of peptide research and therapeutics, 2005-06, Vol.11 (2), p.117-123

2005

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Peptide antagonists of the calcitonin gene-related peptide (CGRP) receptor with improved pharmacokinetics and pharmacodynamics

Biopolymers, 2013-07, Vol.100 (4), p.422-430

2013

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A Chemical Approach to the Pharmaceutical Optimization of an Anti-HIV Protein

Journal of the American Chemical Society, 2007-10, Vol.129 (43), p.13153-13159

2007

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A New Approach to the Chemical Synthesis of Keto-Proteins

Journal of the American Chemical Society, 2003-11, Vol.125 (47), p.14238-14239

2003

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Synthesis of Difficult Cyclic Peptides by Inclusion of a Novel Photolabile Auxiliary in a Ring Contraction Strategy

Journal of the American Chemical Society, 1999-10, Vol.121 (42), p.9790-9796

1999

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An Activated O → N Acyl Transfer Auxiliary: Efficient Amide-Backbone Substitution of Hindered “Difficult” Peptides

Journal of organic chemistry, 2000-09, Vol.65 (18), p.5460-5468

2000

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Three-Dimensional Solution Structure of α-Conotoxin MII by NMR Spectroscopy: Effects of Solution Environment on Helicity

Biochemistry (Easton), 1998-11, Vol.37 (45), p.15621-15630

1998

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Unichemo Protection: A Concept for Chemical Synthesis This work was supported by the Danish National Research Foundation

Angewandte Chemie International Edition, 2001-10, Vol.40 (19), p.3655-3657

2001

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Graphical Abstract

Angewandte Chemie International Edition, 2001-10, Vol.40 (19), p.3489-3489

2001

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Cover Image, Volume 116, Number 9, September 2019

Biotechnology and bioengineering, 2019-09, Vol.116 (9), p.i-i

2019

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Epitope Discovery for a Synthetic Polymer Nanoparticle: A New Strategy for Developing a Peptide Tag

Utilization of tyrosine- and histidine-containing dipeptides to enhance productivity and culture viability

Development of human-machine language interfaces for the visual analysis of complex biologics and RNA modalities and associated experimental data

Identification of Antibody and Small Molecule Antagonists of Ferroportin-Hepcidin Interaction

Structure-guided Discovery of Dual-recognition Chemibodies

Engineering Potent and Selective Analogues of GpTx-1, a Tarantula Venom Peptide Antagonist of the NaV1.7 Sodium Channel

Accelerating attribute‐focused process and product development through the development and deployment of autonomous process analytical technology platform system

Process development of a SARS-CoV-2 nanoparticle vaccine

Metal-Free Polymer-Based Affinity Medium for Selective Purification of His6-Tagged Proteins

Discovery of Tarantula Venom-Derived NaV1.7-Inhibitory JzTx‑V Peptide 5‑Br-Trp24 Analogue AM-6120 with Systemic Block of Histamine-Induced Pruritis

Half-life extension of peptidic APJ agonists by N-terminal lipid conjugation

Accelerated Chemical Synthesis of Peptides and Small Proteins

Use of Cryopreserved Hepatocytes as Part of an Integrated Strategy to Characterize In Vivo Clearance for Peptide-Antibody Conjugate Inhibitors of Nav1.7 in Preclinical Species

Discovery of Tarantula Venom-Derived Na V 1.7-Inhibitory JzTx-V Peptide 5-Br-Trp24 Analogue AM-6120 with Systemic Block of Histamine-Induced Pruritis

Engineering Antibody Reactivity for Efficient Derivatization to Generate NaV1.7 Inhibitory GpTx‑1 Peptide–Antibody Conjugates

Fmoc-Protein Synthesis: Preparation of Peptide Thioesters Using a Side-Chain Anchoring Strategy

Peptide antagonists of the calcitonin gene-related peptide (CGRP) receptor with improved pharmacokinetics and pharmacodynamics

A Chemical Approach to the Pharmaceutical Optimization of an Anti-HIV Protein

A New Approach to the Chemical Synthesis of Keto-Proteins

Synthesis of Difficult Cyclic Peptides by Inclusion of a Novel Photolabile Auxiliary in a Ring Contraction Strategy

An Activated O → N Acyl Transfer Auxiliary: Efficient Amide-Backbone Substitution of Hindered “Difficult” Peptides

Three-Dimensional Solution Structure of α-Conotoxin MII by NMR Spectroscopy: Effects of Solution Environment on Helicity

Unichemo Protection: A Concept for Chemical Synthesis This work was supported by the Danish National Research Foundation

Graphical Abstract

Cover Image, Volume 116, Number 9, September 2019

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