We use theoretical and computational techniques to help solve biological and medical problems. Our current research topics can be grouped into four categories: Gene discovery. We analyze the Expressed Sequence Tag (EST) DNA sequence database to discover genes that are specifically expressed in a particular organ or tumor. The products of such genes can potentially be used as targets for delivery of antitumor agents, for anticancer vaccine development, and for tumor imaging. This is a collaboration with Dr. Ira Pastan's Molecular Biology Section. Immunotoxins. Immunotoxins are man-made molecules constructed by joining an anti-cancer antibody and a suitable toxin, in our case, the pseudomonas exotoxin A. Ideally, these molecules will bind only to the target cancer cells and kill them. There are many such designed molecules, each having a specific antibody for a particular cancer. Some of these molecules, made by Dr. Pastan's laboratory, produced highly encouraging results during the phase I clinical trials. We study these molecules and design mutations that will alter/improve their properties as an effective drug. This is also a collaborative work with Dr. Pastan's laboratory. Protein structure. We study surface areas, volumes, and cavities in protein structures. Currently, we are working on developing potentials for ab initio folding and on procedures for automatic domain identification and structure-based protein classification. Hydrophobicity. We study the phenomenon of hydrophobicity by means of statistical thermodynamics. The hydrophobic effect is believed to be one of the main forces that determine the structure, stability, and interaction of protein and other biologically important molecules.

Agency
National Institute of Health (NIH)
Institute
Division of Basic Sciences - NCI (NCI)
Type
Intramural Research (Z01)
Project #
1Z01BC008759-12
Application #
6950514
Study Section
(LMB)
Project Start
Project End
Budget Start
Budget End
Support Year
12
Fiscal Year
2003
Total Cost
Indirect Cost
Name
Basic Sciences
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Das, Sudipto; Hahn, Yoonsoo; Walker, Dawn A et al. (2008) Topology of NGEP, a prostate-specific cell:cell junction protein widely expressed in many cancers of different grade level. Cancer Res 68:6306-12
Hahn, Yoonsoo; Jeong, Sangkyun; Lee, Byungkook (2007) Inactivation of MOXD2 and S100A15A by exon deletion during human evolution. Mol Biol Evol 24:2203-12
Das, Sudipto; Hahn, Yoonsoo; Nagata, Satoshi et al. (2007) NGEP, a prostate-specific plasma membrane protein that promotes the association of LNCaP cells. Cancer Res 67:1594-601
Grigoryev, Dmitry N; Ma, Shwu-Fan; Shimoda, Larissa A et al. (2007) Exon-based mapping of microarray probes: recovering differential gene expression signal in underpowered hypoxia experiment. Mol Cell Probes 21:134-9
Bera, Tapan K; Saint Fleur, Ashley; Lee, Yoomi et al. (2006) POTE paralogs are induced and differentially expressed in many cancers. Cancer Res 66:52-6
Hahn, Yoonsoo; Lee, Byungkook (2006) Human-specific nonsense mutations identified by genome sequence comparisons. Hum Genet 119:169-78
Sam, Vichetra; Tai, Chin-Hsien; Garnier, Jean et al. (2006) ROC and confusion analysis of structure comparison methods identify the main causes of divergence from manual protein classification. BMC Bioinformatics 7:206
Hahn, Yoonsoo; Bera, Tapan K; Pastan, Ira H et al. (2006) Duplication and extensive remodeling shaped POTE family genes encoding proteins containing ankyrin repeat and coiled coil domains. Gene 366:238-45
Egland, Kristi A; Liu, Xiu Fen; Squires, Stephen et al. (2006) High expression of a cytokeratin-associated protein in many cancers. Proc Natl Acad Sci U S A 103:5929-34
Hahn, Yoonsoo; Lee, Byungkook (2005) Identification of nine human-specific frameshift mutations by comparative analysis of the human and the chimpanzee genome sequences. Bioinformatics 21 Suppl 1:i186-94

Showing the most recent 10 out of 29 publications