The variable domain of the new antigen receptor (V ) of shark single domain antibodies is evolutionarily distant from the variable regions (V ) of mammalian immunoglobulins, yet it still has complementarity-determining regions (CDRs) that are involved in antigen recognition, therefore making it possible to humanize by grafting these CDRs to the framework of human V homologs. Here, we show the V CDR based on an analysis of currently available V -antigen structure complexes in the global Protein Data Bank archive of 3D structure data, and describe the detailed protocol to humanize V by CDR grafting, using B6 (an anti-Pseudomonas exotoxin V ), the most common type (Type II) of shark V s, as an example. Ongoing efforts will further optimize the protocol for moving shark V s to the clinic for treating cancer and other human diseases. Published 2023. This article is a U.S. Government work and is in the public domain in the USA. Basic Protocol: Humanize shark V sequence by CDR grafting Support Protocol 1: V structure prediction and comparison Support Protocol 2: Measure binding kinetics of humanized V using bio-layer interferometry (BLI).
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http://dx.doi.org/10.1002/cpz1.630 | DOI Listing |
Diagnostics (Basel)
January 2025
Department of Interdisciplinary Medicine, University of Bari "Aldo Moro", 70121 Bari, Italy.
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Production and R&D Center I of LSS (Life Science Service), GenScript Biotech Corporation, No. 28, Yongxi Rd., Nanjing, 211100, Jiangsu, China.
The application of antibody therapeutics is promising in the field of immunotherapy. While, heterologization should be done in most cases before applying the therapeutic antibodies into bodies, e.g.
View Article and Find Full Text PDFNeoplasia
January 2025
Division of Hematology-Oncology, Pediatric Hematology-Oncology Center, Zhejiang Provincial Research Center for Childhood Leukemia New Diagnostic and Therapeutic Techniques, Children's Hospital, Zhejiang University School of Medicine, National Clinical Medical Research Center for Child Health, #57 Zhugan Road, Yan-an Street, Hangzhou 310006, China. Electronic address:
Leukemia stem cells (LSCs) play a critical role in the initiation, recurrence, and resistance to treatment of leukemia. Eradicating LSCs is crucial for the complete elimination of the disease. CD45RA is identified as an important marker for LSC subsets in acute myeloid leukemia (AML), providing a strategic target for therapy.
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November 2024
Faculty of Molecular Chemistry and Engineering, Kyoto Institute of Technology, Kyoto, Japan. Electronic address:
Most of currently available sandwich-type enzyme-linked immunosorbent assays (ELISA) require the use of full-length animal-derived antibodies which poses welfare criticisms and are often expensive to produce. There is therefore a strong demand for the development of more affordable and animal-free methods to produce antibodies for sandwich ELISA assay. To address these issues, we propose here the development of a new technology based on two complementary rabbit single-chain variable fragments (scFvs) and an Ig-binding domain of protein L (PpL1) fused to a polystyrene-binding peptide (PS-tag) that can be recombinantly produced in bacteria.
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October 2024
Department of Hematology, University Hospital Vall d'Hebron, Barcelona, Spain.
Chimeric antigen receptor (CAR) T-cell therapy fails to achieve durable responses in over 60% of relapsed/refractory (R/R) large B-cell lymphoma (LBCL) patients in the third or later line setting. After CAR-T failure, survival outcomes are heterogeneous and a prognostic model in this patient population is lacking. A training cohort of 216 patients with progressive disease (PD) after CAR-T from 12 Spanish centers was used to develop the Post-CAR Prognostic Index (PC-PI); primary endpoint was overall survival (OS) from CAR-T progression.
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