Double mutants of dihydrofolate reductase and methods of using same
AssigneeSloan-Kettering Institute for Cancer Research
InventorsJoseph R. Bertino, Emine A. Ercikan-Abali, Debabrata Banerjee, Shin Mineishi, Michel Sadelain
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Abstract
New mutant forms of human dihydrofolate reductase (DHFR) which have properties superior to the previously disclosed mutants have mutations at both amino acid 22 and amino acid 31. Specific mutant forms are Ser31Tyr22, Ser31Phe22, Gly31Tyr22, Gly31Phe22, Ala31Tyr22 and Ala31Phe22. The mutant DHFR of the invention may be used as a selectable marker, and to modify the genome of human cells, particularly bone marrow cells or peripheral blood stem cells, to render them resistant to chemotherapy using antifolate agents.
Claims8
A method for reducing the toxic effects of antifolate therapy on human cells comprising the step of introducing into the cells an expressible mutant form of human dihydrofolate reductase which differs from wild-type human dihydrofolate reductase as defined by Seq ID No. 7 at both amino acid 22 and amino acid 31, wherein the mutant form has an uncharged amino acid with a larger volume side chain than leucine at amino acid 22 and an amino acid which having a smaller volume more hydrophilic side chain than phenylalanine at amino acid 31.
A method for reducing the toxic effects of antifolate therapy in a human patient, comprising the steps of
- (a) obtaining hematopoietic cells from the patient;
- (b) transducing into the hematopoietic cells an expressible mutant form of human dihydrofolate reductase which differs from wild-type human dihydrofolate reductase as defined by Seq ID No. 7 at both amino acid 22 and amino acid 31, wherein the mutant form has an uncharged amino acid with a larger volume side chain than leucine at amino acid 22 and an amino acid which having a smaller volume, more hydrophilic side chain than phenylalanine at amino acid 31;
- and
- (c) returning the transduced cells to the human patient.
Dependencies are inferred from the claim text.