![]() | Donald CramptonBiochemistry, Molecular Biology Assistant Professor of ChemistryClark University Worcester, MA 01610-1477 E-mail: dcrampton@clarku.edu Phone: 508-793-7553 Office: S226, Sackler Sciences Center |
| B.A., Biochemistry, Ithaca College, 1994 Ph.D., Botany, Arizona State University, 2000 Postdoctoral Fellow, Harvard Medical School, 2001-2005 Instructor, Harvard Medical School, 2005-2006 Dr. Crampton has held appointments at Boston College and Tufts University. Current Research and TeachingResearch in our laboratory is organized around bacterophage, viruses that infect and kill bacteria. Bacteriophage (or phage) represent the largest depository of genomic DNA in the biosphere with an estimate of 1031 or more individual bacteriophase on the earth. Phage also have an integral role in molecular biology -- for example, restriction enzymes evolved as a bacterial defense against phage infection and enzymes such as ligase and polynucleotide kinase come from phage-encoded genes. In the Crampton Laboratory, we have two bacteriophage related research areas: mitochondrial DNA replication and discovery of bacteriophage specific for disease causing bacteria. Mitochondrial DNA ReplicationMitochondria are the energy producing organelle in the cell, and the only organelle in animal cells besides the nucleus that contains its own chromosome. Given the bacterial ancestry of mitochondria, one might expect that the essential elements of genome maintenance would resemble those of bacteria. However, this is not the case for the DNA polymerase or the replicative helicase, which appear to have a shared ancestry with proteins of T-odd bacteriophages. Bacteriophage DiscoveryOur other project relies on two widely held beliefs about bacteriophage. First, phage population densities exceed bacterial densities by a ratio of 10-to-1 or more. Hence, bacteriophage represent a huge repository of genomic wealth consisting of gene products with unknown but potentially useful functions. Second, bacteriophages have evolved unique proteins that arrest critical cellular processes to commit bacterial host metabolism to phage reproduction. MiscellaneousCourses that I am involved in include Biochemistry, Bioanalytical Cemistry, Protein Chemistry, and Forensics. I am also an active member of the American Society for Biochemistry and Molecular Biology and the Council for Undergraduate Research. Selected Publications“Oligomeric States of the Bacteriophage T7 Helicase-Primase,” Donald J. Crampton, Melanie Ohi, Udi Qimron, Thomas Walz, and Charles C. Richardson (2006). Journal of Molecular Biology 360, 667-677. “DNA-induced Switch from Independent to Sequential dTTP Hydrolysis in the Bacteriophage T7 Helicase,” Donald J. Crampton, Sourav Mukherjee, and Charles C. Richardson (2006). Molecular Cell 21, 165-174. “The Arginine Finger of Bacteriophage T7 Gene 4 Helicase: Role in Energy Coupling,” Donald J. Crampton, Shenyuan Guo, Donald E. Johnson, and Charles C. Richardson (2003). Proceedings of the National Academy of Sciences (USA) 101, 4373-4378. “Single-molecule kinetics of lambda exonuclease reveal base dependence and dynamic disorder,” Antoine van Oijen, Paul C. Blainey, Donald J. Crampton, Charles C. Richardson, Tom Ellenberger, and X. Sunney Xie (2003). Science 301, 1235-1238. |

