cytochrome
About the DepartmentFaculty & ResearchGraduateUndergraduateCoursesSeminarsOutreachAlumni
--
Faculty Research Interests
--
Affiliates
--
Lecturers
--
Faculty Office Hours
--
Faculty Awards
--
NMR/Mass Spec Facilities
--
Reserve NMR
--
Reserve Mass Spec
--
X-Ray Facility
--
X-Ray Crystallography
--
Resources
--


Chemistry and Biochemistry
University of California
230 Physical Sciences Bldg.
Santa Cruz, CA 95064
Phone: (831) 459-4002
Fax: (831) 459-2935
Email
Maps & Directions

A-Z Index | Find People

 

Related Links:
RNA Center
Center for Biomolecular Science
MCD Biology
EEB Biology
Environmental Toxicology
Ocean Sciences
Physics
Division of Physical & Biological Sciences
UCSC Home
Science Library
McHenry Library
Environmental Health & Safety

David W. Deamer  

David W. Deamer
Professor Emeritus of Chemistry (Recalled)
B.S., Duke University
Ph.D., Ohio State University School of Medicine

Office: 405 PSB
Phone: (831) 459-5158
Fax: (831) 459-2935
deamer@chemistry.ucsc.edu

  Deamer Research Group
Department of Chemistry
University of California
1156 High Street
Santa Cruz, CA 95064

Office Hours
Class Times & Locations
Labs: 290 PSB, 9-5157

RESEARCH INTERESTS: Membrane Biophysics, Model Membrane Systems, Membrane Transport Mechanisms, Molecular Self-Assembly Processes

David Deamer's primary research area concerns the manner in which linear macromolecules traverse nanoscopic channels. Single-stranded nucleic acid molecules can be driven electrophoretically through a large channel embedded in a lipid-bilayer membrane, and the presence of the polynucleotide in the channel affects the ionic conductance in a manner related to chain length and concentration. This observation has considerable potential for characterizing DNA and RNA in microscopic volumes of nucleic acid solutions. (See Akeson et al. 1999 and Vercoutere et al. 2001 for recent reports.)

A second line of research concerns molecular self-assembly processes related to the structure and function of biological membranes, and particularly the origin and evolution of membrane structure. One example of such research was reported recently by Dworkin et al. (2001) in which it was shown that photochemical reactions simulating those occurring in the interstellar medium give rise to amphiphilic molecules that can self-assemble into membrane structures. Apel et al. (2001) and Monnard et al., (2002) went on to show that membranes can self-assemble for simple amphiphiles such as fatty acids and alcohols, and that such processes are markedly affected by ionic content of the environment. (See figure). These results help us to understand how primitive forms of cellular life appeared on the early Earth and were able to capture nutrients from the surrounding medium and incorporate them in intracellular growth processes.

Decanoic acid is a simple amphiphilic molecule that can assemble into membranous vesicles such as those shown above on the left. However, in the presence of salt solutions such as sea water, the vesicles collapse and aggregate, suggesting that the membranes of the first cellular life required a fresh-water environment for stability. Monnard et al. 2002.

SELECTED PUBLICATIONS

J. P. Dworkin, D. W. Deamer, S. A. Sandford, and L. J. Allamandola. 2001. Self-assembling amphiphilic molecules: Synthesis in simulated interstellar/precometary ices. Proc. Natl. Acad. Sci. USA 98:815-819.

Vercoutere, W., S. Winters-Hilt, H. Olsen, D.W. Deamer. D. Haussler, and M. Akeson. 2001. Rapid discrimination among individual DNA molecules at single nucleotide resolution using a nanopore instrument. Nature Biotechnology 19: 248-250.

Deamer D, Dworkin JP, Sandford SA, Bernstein MP, Allamandola LJ. The first cell membranes. 2002. Astrobiology. 2:371-81.

Winters-Hilt, S., W. Vercoutere, V. S. DeGuzman, D. Deamer, M. Akeson & D. Haussler. 2003. Highly accurate classification of Watson-Crick base-pairs on termini of single DNA molecules Biophys. J. 84:967-76.

Vercoutere, W.A., S. Winters-Hilt, V. S. DeGuzman, D. Deamer, S. Ridino, J. T. Rodgers, H. E. Olsen, A. Marziali, and M. Akeson. 2003. Discrimination among individual Watson-Crick base-pairs at the termini of single DNA hairpin molecules. Nucleic Acids Research 31:1311-1318.

Rasmussen S, Chen L, Deamer D, Krakauer DC, Packard NH, Stadler PF, Bedau MA. 2004. Evolutionary transitions from nonliving to living matter. Science. 303:963-5.

Veronica S. DeGuzman, Clarence C. Lee, Wenonah A. Vercoutere, Steven Winters-Hilt, AndrŽ Marziali, Mark Akeson and David W. Deamer 2006. Sequence-dependent gating of an ion channel by DNA hairpin molecules. Nucleic Acids Research 34:6425-37.

Monnard, P.-A., Luptak, A. and Deamer, D.W. 2007. Models of primitive cellular life: polymerases and templates in liposomes. Phil. Trans. B, Royal Society. (In press)

D. Yin, J.P. Barber, D.W. Deamer, A.R. Hawkins, and H. Schmidt, 2006. Single-molecule detection sensitivity using planar integrated optics on a chip", Optics Letters 31, 2136.

D. Yin, E.J. Lunt, M.I. Rudenko, D.W. Deamer, A.R. Hawkins, and H. Schmidt. 2007. Planar optofluidic chip for single particle detection, manipulation, and analysis, Lab on Chip 7, 1171.

Benner, S. Chen, R.J., Wilson, N., AbuShuays, R., Hurt, N., Lieberman, K., Deamer, D.W., Dunbar, W.B. and Akeson, M. 2007. Sequence-specific detection of individual DNA polymerase complexes in real time using a nanopore. Nature Nanotechnology (In press. Epub October 2007)

alt
About the Department | Faculty | Research | Graduate | Undergraduate | Courses | News and Events | Outreach | Alumni
Page Maintained by webmaster@chemistry.ucsc.edu| Last Reviewed 11/6/07 | © 2006 UC Santa Cruz