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Synthesis of site-specific antibody-drug conjugates using unnatural amino acids
Antibody-drug conjugates (ADCs) allow selective targeting of cytotoxic drugs to cancer cells presenting tumor-associated surface markers, thereby minimizing systemic toxicity. Traditionally, the drug is conjugated nonselectively to cysteine or lysine residues in the antibody. However, these strategi...
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| Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
National Academy of Sciences
2012
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3479532/ https://ncbi.nlm.nih.gov/pubmed/22988081 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1211023109 |
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