The long term objective of my research is to describe the precise molecular structure and function of lysosomes. From biosynthesis to turnover, how do lysosomes assemble, organize and activate their constituent enzymes, while protecting the cell from autodigestion? Within this general framework, the proposed experiments will specifically ask: 1) what protein sequence determinants of cathepsin D, a major lysosomal protease, and pepsin, a secreted protease, are responsible for directing these two highly homologous digestive enzymes to different cellular compartments; ii) what are the general cellular effects of a loss of cathepsin D activity in lysosomes; iii) what is the physical disposition of cathepsin D in the various cellular compartments including lysosomes, i.e. is it membrane bound or soluble; and iv) what parameters define cathepsin D turnover or degradation? To answer these questions it will be necessary to isolate functionally expressible recombinant DNA molecules coding for cathepsin D and pepsin and isolate cultured cells conditionally defective in cathepsin D activity. The recombinant clones will be used to construct deletion and fusion proteins which will, in turn, be assayed for complementation of the cathepsin D deficient cells. This approach will allow rapid screening of randomly constructed (i.e. shotgun) recombinant molecules and thus, a complete search of cathepsin D and pepsin primary sequence for putative sorting signals. To evaluate the effect of a loss of cathepsin D activity, the conditionally defective cells will be characterized in terms of their biochemical defect, changes in protein synthesis and turnover, morphology, and growth characteristics. Pulse-chase cell fractionation procedures will be used to study the turnover of cathepsin D as it relates to lysosome structure and function in normal cultured cells. The studies of lysosome physiology, described here, are basic in nature but will be valuable to our understanding of lysosome related pathologies at the cellular and molecular level.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM035812-04
Application #
3289086
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1986-01-01
Project End
1990-12-31
Budget Start
1989-01-01
Budget End
1989-12-31
Support Year
4
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Miami School of Medicine
Department
Type
Schools of Medicine
DUNS #
City
Miami
State
FL
Country
United States
Zip Code
33101