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Ira Pastan

Researcher at Laboratory of Molecular Biology

Publications -  1304
Citations -  113191

Ira Pastan is an academic researcher from Laboratory of Molecular Biology. The author has contributed to research in topics: Immunotoxin & Pseudomonas exotoxin. The author has an hindex of 160, co-authored 1286 publications receiving 110069 citations. Previous affiliations of Ira Pastan include Heidelberg University & National Institutes of Health.

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Receptor-mediated endocytosis of alpha 2-macroglobulin in cultured fibroblasts.

TL;DR: Alpha 2-macroglobulin is internalized into cultured fibroblasts by receptor-mediated endocytosis and interacts with the Golgi-endoplasmic reticulum-lysosome system in the cell to deliver the ligand to newly formed lysosomes within 30--60 min.
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Coexpression of a multidrug-resistance gene (MDR1) and herpes simplex virus thymidine kinase gene as part of a bicistronic messenger RNA in a retrovirus vector allows selective killing of MDR1-transduced cells

TL;DR: A safety-modified vector, pSXLC/pHa, was constructed to coexpress drug-selectable markers with a second gene of interest as a part of a bicistronic mRNA in a retroviral vector using an internal ribosome entry site (IRES) from encephalomyocarditis virus.
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Effect of chelator conjugation level and injection dose on tumor and organ uptake of 111In-labeled MORAb-009, an anti-mesothelin antibody.

TL;DR: It is demonstrated that the number of chelate conjugation and the injected dose are two important parameters to achieve high tumor and low non-target organ uptake of (111)In-labeled MORAb-009 and suggested that the injected doses of mAb could be individualized based on the tumor size or the blood level of shed antigen in a patient to achieve the ideal tumor-to-organ radioactivity ratios.
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Cyclic AMP, the Cyclic AMP Receptor Protein, and Their Dual Control of the Galactose Operon

TL;DR: This paper summarizes the experimental evidence which led to the demonstration of the role of cyclic AMP and its receptor protein (CRP) in the activation of gene transcription in bacteria and examines its function in the control of the galactose operon of Escherichia coli.
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Comparison of recombinant immunotoxins against LeY antigen expressing tumor cells: influence of affinity, size, and stability.

TL;DR: The smaller size of the Fab immunotoxins compared to B3Lys-PE38 and the increased T1/2 value compared toB3(scFv)- PE38 and B3(dsFV)-PE38 make these recombinant immunotoxinins alternative therapeutic agents to treat Ley antigen positive cancers.