5FCS
Diabody
Summary for 5FCS
Entry DOI | 10.2210/pdb5fcs/pdb |
Descriptor | Diabody, SULFATE ION, ... (4 entities in total) |
Functional Keywords | antibody, diabody, pcad, cd3, immune system |
Biological source | Homo sapiens More |
Total number of polymer chains | 2 |
Total formula weight | 53544.86 |
Authors | Mosyak, L.,Root, A. (deposition date: 2015-12-15, release date: 2016-12-14, Last modification date: 2024-10-23) |
Primary citation | Root, A.R.,Cao, W.,Li, B.,LaPan, P.,Meade, C.,Sanford, J.,Jin, M.,O'Sullivan, C.,Cummins, E.,Lambert, M.,Sheehan, A.D.,Ma, W.,Gatto, S.,Kerns, K.,Lam, K.,D'Antona, A.M.,Zhu, L.,Brady, W.A.,Benard, S.,King, A.,He, T.,Racie, L.,Arai, M.,Barrett, D.,Stochaj, W.,LaVallie, E.R.,Apgar, J.R.,Svenson, K.,Mosyak, L.,Yang, Y.,Chichili, G.R.,Liu, L.,Li, H.,Burke, S.,Johnson, S.,Alderson, R.,Finlay, W.J.J.,Lin, L.,Olland, S.,Somers, W.,Bonvini, E.,Gerber, H.P.,May, C.,Moore, P.A.,Tchistiakova, L.,Bloom, L. Development of PF-06671008, a Highly Potent Anti-P-cadherin/Anti-CD3 Bispecific DART Molecule with Extended Half-Life for the Treatment of Cancer. Antibodies, 5:-, 2016 Cited by PubMed Abstract: Bispecific antibodies offer a promising approach for the treatment of cancer but can be challenging to engineer and manufacture. Here we report the development of PF-06671008, an extended-half-life dual-affinity re-targeting (DART) bispecific molecule against P-cadherin and CD3 that demonstrates antibody-like properties. Using phage display, we identified anti-P-cadherin single chain Fv (scFv) that were subsequently affinity-optimized to picomolar affinity using stringent phage selection strategies, resulting in low picomolar potency in cytotoxic T lymphocyte (CTL) killing assays in the DART format. The crystal structure of this disulfide-constrained diabody shows that it forms a novel compact structure with the two antigen binding sites separated from each other by approximately 30 Å and facing approximately 90° apart. We show here that introduction of the human Fc domain in PF-06671008 has produced a molecule with an extended half-life (-4.4 days in human FcRn knock-in mice), high stability (T1 > 68 °C), high expression (>1 g/L), and robust purification properties (highly pure heterodimer), all with minimal impact on potency. Finally, we demonstrate anti-tumor efficacy in a human colorectal/human peripheral blood mononuclear cell (PBMC) co-mix xenograft mouse model. These results suggest PF-06671008 is a promising new bispecific for the treatment of patients with solid tumors expressing P-cadherin. PubMed: 31557987DOI: 10.3390/antib5010006 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.01 Å) |
Structure validation
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