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Semi-synthetic vNAR libraries screened against therapeutic antibodies primarily deliver anti-idiotypic binders

Scientific reports, 2017-08, Vol.7 (1), p.9676-13, Article 9676

2017

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From strain engineering to process development: monoclonal antibody production with an unnatural amino acid in Pichia pastoris

Microbial cell factories, 2022-08, Vol.21 (1), p.1-16, Article 157

2022

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A Generic Approach for Miniaturized Unbiased High-Throughput Screens of Bispecific Antibodies and Biparatopic Antibody-Drug Conjugates

International journal of molecular sciences, 2024-02, Vol.25 (4), p.2097

2024

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Shark Strikes Twice: Hypervariable Loop 2 of Shark IgNAR Antibody Variable Domains and Its Potential to Function as an Autonomous Paratope

Marine biotechnology (New York, N.Y.), 2015-08, Vol.17 (4), p.386-392

2015

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Cystine-knot peptides targeting cancer-relevant human cytotoxic T lymphocyte-associated antigen 4 (CTLA-4)

Journal of peptide science, 2015-08, Vol.21 (8), p.651-660

2015

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Site-Specific Antibody-Drug Conjugation Using Microbial Transglutaminase

Methods in molecular biology (Clifton, N.J.), 2019-01, Vol.2012, p.135

2019

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EGFR binding Fc domain-drug conjugates: stable and highly potent cytotoxic molecules mediate selective cell killing

Biological chemistry, 2022-04, Vol.403 (5-6), p.525

2022

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Sortagged anti-EGFR immunoliposomes exhibit increased cytotoxicity on target cells

European journal of pharmaceutics and biopharmaceutics, 2019-03, Vol.136, p.203-212

2019

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Site-Specific Conjugation of Thiol-Reactive Cytotoxic Agents to Nonnative Cysteines of Engineered Monoclonal Antibodies

Methods in molecular biology (Clifton, N.J.), 2019, Vol.2033, p.1

2019

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Welding PROxAb Shuttles: A Modular Approach for Generating Bispecific Antibodies via Site-Specific Protein–Protein Conjugation

Bioconjugate chemistry, 2024-06, Vol.35 (6), p.780-789

2024

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Effect of Conjugation Site and Technique on the Stability and Pharmacokinetics of Antibody-Drug Conjugates

Journal of pharmaceutical sciences, 2021-12, Vol.110 (12), p.3776-3785

2021

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Efficient spontaneous site-selective cysteine-mediated toxin attachment within a structural loop of antibodies

Biochimica et biophysica acta. General subjects, 2022-07, Vol.1866 (7), p.130155-130155, Article 130155

2022

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Site-Specific Conjugation of Native Antibodies Using Engineered Microbial Transglutaminases

Bioconjugate chemistry, 2020-04, Vol.31 (4), p.1070-1076

2020

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Engineering bispecific antibodies with defined chain pairing

New biotechnology, 2017-10, Vol.39 (Pt B), p.167-173

2017

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Potent antitumor activity of anti-HER2 antibody-topoisomerase I inhibitor conjugate based on self-immolative dendritic dimeric-linker

Journal of controlled release, 2024-03, Vol.367, p.148-157

2024

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An Apoptosis-Inducing Peptidic Heptad That Efficiently Clusters Death Receptor5

Angewandte Chemie International Edition, 2016-04, Vol.55 (16), p.5085

International ed. in English, 2016

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An Apoptosis-Inducing Peptidic Heptad That Efficiently Clusters Death Receptor 5

Angewandte Chemie (International ed.), 2016-04, Vol.55 (16), p.5085-5089

2016

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Isolation of Anti-Hapten Antibodies by Fluorescence-Activated Cell Sorting of Yeast-Displayed B-Cell Receptor Gene Repertoires

Methods in molecular biology (Clifton, N.J.), 2020-01, Vol.2070, p.267

2020

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Self-Assembled Hybrid Aptamer-Fc Conjugates for Targeted Delivery: A Modular Chemoenzymatic Approach

ACS chemical biology, 2015-09, Vol.10 (9), p.2158-2165

2015

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Locked by Design: A Conformationally Constrained Transglutaminase Tag Enables Efficient Site-Specific Conjugation

Angewandte Chemie (International ed.), 2015-11, Vol.54 (45), p.13420-13424

International ed. in English, 2015

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Engineering bispecific antibodies with defined chain pairing

New biotechnology, 2017-10, Vol.39 (Part B), p.167

2017

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Ein Apoptose-induzierendes Heptamer, das effizient den Todesrezeptor5 bundelt

Angewandte Chemie, 2016-04, Vol.128 (16), p.5169

2016

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Ein Apoptose-induzierendes Heptamer, das effizient den Todesrezeptor 5 bündelt

Angewandte Chemie, 2016-04, Vol.128 (16), p.5169-5173

2016

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Durch Design verbrückt: ein konformativ eingeschränkter Transglutaminase-Marker ermöglicht effiziente ortsspezifische Konjugation

Angewandte Chemie, 2015-11, Vol.127 (45), p.13618-13623

2015

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Ein Apoptose‐induzierendes Heptamer, das effizient den Todesrezeptor 5 bündelt

Angewandte Chemie, 2016-04, Vol.128 (16), p.5169-5173

2016

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Semi-synthetic vNAR libraries screened against therapeutic antibodies primarily deliver anti-idiotypic binders

From strain engineering to process development: monoclonal antibody production with an unnatural amino acid in Pichia pastoris

A Generic Approach for Miniaturized Unbiased High-Throughput Screens of Bispecific Antibodies and Biparatopic Antibody-Drug Conjugates

Shark Strikes Twice: Hypervariable Loop 2 of Shark IgNAR Antibody Variable Domains and Its Potential to Function as an Autonomous Paratope

Cystine-knot peptides targeting cancer-relevant human cytotoxic T lymphocyte-associated antigen 4 (CTLA-4)

Site-Specific Antibody-Drug Conjugation Using Microbial Transglutaminase

EGFR binding Fc domain-drug conjugates: stable and highly potent cytotoxic molecules mediate selective cell killing

Sortagged anti-EGFR immunoliposomes exhibit increased cytotoxicity on target cells

Site-Specific Conjugation of Thiol-Reactive Cytotoxic Agents to Nonnative Cysteines of Engineered Monoclonal Antibodies

Welding PROxAb Shuttles: A Modular Approach for Generating Bispecific Antibodies via Site-Specific Protein–Protein Conjugation

Effect of Conjugation Site and Technique on the Stability and Pharmacokinetics of Antibody-Drug Conjugates

Efficient spontaneous site-selective cysteine-mediated toxin attachment within a structural loop of antibodies

Site-Specific Conjugation of Native Antibodies Using Engineered Microbial Transglutaminases

Engineering bispecific antibodies with defined chain pairing

Potent antitumor activity of anti-HER2 antibody-topoisomerase I inhibitor conjugate based on self-immolative dendritic dimeric-linker

An Apoptosis-Inducing Peptidic Heptad That Efficiently Clusters Death Receptor5

An Apoptosis-Inducing Peptidic Heptad That Efficiently Clusters Death Receptor 5

Isolation of Anti-Hapten Antibodies by Fluorescence-Activated Cell Sorting of Yeast-Displayed B-Cell Receptor Gene Repertoires

Self-Assembled Hybrid Aptamer-Fc Conjugates for Targeted Delivery: A Modular Chemoenzymatic Approach

Locked by Design: A Conformationally Constrained Transglutaminase Tag Enables Efficient Site-Specific Conjugation

Engineering bispecific antibodies with defined chain pairing

Ein Apoptose-induzierendes Heptamer, das effizient den Todesrezeptor5 bundelt

Ein Apoptose-induzierendes Heptamer, das effizient den Todesrezeptor 5 bündelt

Durch Design verbrückt: ein konformativ eingeschränkter Transglutaminase-Marker ermöglicht effiziente ortsspezifische Konjugation

Ein Apoptose‐induzierendes Heptamer, das effizient den Todesrezeptor 5 bündelt

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