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Competency development in antibody production in cancer cell biology

Description: This is the final report of a three-year, Laboratory Directed Research and Development (LDRD) project at Los Alamos National Laboratory (LANL). The main objective of this project was to develop a rapid recombinant antibody production technology. To achieve the objective, the authors employed (1) production of recombinant antigens that are important for cell cycle regulation and DNA repair, (2) immunization and specific selection of antibody-producing lymphocytes using the flow cytometry and magnetic bead capturing procedure, (3) construction of single chain antibody library, (4) development of recombinant vectors that target, express, and regulate the expression of intracellular antibodies, and (5) specific inhibition of tumor cell growth in tissue culture. The authors have accomplished (1) optimization of a selection procedure to isolate antigen-specific lymphocytes, (2) optimization of the construction of a single-chain antibody library, and (3) development of a new antibody expression vector for intracellular immunization. The future direction of this research is to continue to test the potential use of the intracellular immunization procedure as a tool to study functions of biological molecules and as an immuno-cancer therapy procedure to inhibit the growth of cancer cells.
Date: December 1, 1998
Creator: Park, M.S.
Partner: UNT Libraries Government Documents Department

Radiation mutagenesis from molecular and genetic points of view

Description: An important biological effect of ionizing radiation on living organisms is mutation induction. Mutation is also a primary event in the etiology of cancer. The chain events, from induction of DNA damage by ionizing radiation to processing of these damages by the cellular repair/replication machinery, that lead to mutation are not well understood. The development of quantitative methods for measuring mutation-induction, such as the HPRT system, in cultured mammalian cells has provided an estimate of the mutagenic effects of x- and [gamma]-rays as wen as of high LET radiation in both rodent and human cells. A major conclusion from these mutagenesis data is that high LET radiation induces mutations more efficiently than g-rays. Molecular analysis of mutations induced by sparsely ionizing radiation have detected major structural alterations at the gene level. Our molecular results based on analysis of human HPRT deficient mutants induced by [gamma]-rays, [alpha]-particles and high energy charged particles indicate that higher LET radiation induce more total and large deletion mutations than [gamma]-rays. Utilizing molecular techniques including polymerase chain reaction (PCR), Single-strand conformation polymorphism (SSCP), denaturing gradient gel electrophoresis (DGGE) and Direct DNA sequencing, mutational spectra induced by ionizing radiation have been compared in different cell systems. Attempts have also been made to determine the mutagenic potential and the nature of mutation induced by low dose rate [gamma]-rays. Defective repair, in the form of either a diminished capability for repair or inaccurate repair, can lead to increased risk of heritable mutations from radiation exposure. Therefore, the effects of DNA repair deficiency on the mutation induction in mammalian cells is reviewed.
Date: January 1, 1993
Creator: Chen, D.J.C.; Park, M.S.; Okinaka, R.T. & Jaberaboansari, A.
Partner: UNT Libraries Government Documents Department

Factors Controlling In Situ Uranium and Technetium Bioreductionat the NABIR Field Research Center

Description: This research hypotheses is: (1) Indigenous microorganisms in the shallow aquifer at the FRC have the capability to reduce U(VI) and Tc(VII) but rates are limited by--Scarce electron donor, Low pH and potentially toxic metals, and High nitrate. (2) U(VI) and Tc(VII) reduction rates can be increased by--Successive donor additions, Raising pH to precipitate toxic metals, and Adding humics to complex toxic metals and serve as electron shuttles.
Date: March 17, 2004
Creator: Istok, J.; Jones, J.; Park, M.; Sapp, M.; Selko, E.; Laughman, R. et al.
Partner: UNT Libraries Government Documents Department