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To Degrade or Not to Degrade: Substrate Recognition by Lon Protease Amy Dinh Department of Microbiology Mentor: Janine E. Trempy, Ph.D.
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Protein Misfolding Diseases normal protein abnormal protein protein aggregate
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Treatment Issues Aggregates cause disease or caused by disease Cause of abnormal proteins? Result of malfunction of related protein? ADDL aggregates (yellow) coating a neuron in Alzheimer’s Disease. Scientific American
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Studying Human Lon with E. coli lon –ATP dependent protease –highly conserved in evolution –four known substrates in E. coli –NO known substrates in humans
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Aims Study how E. coli Lon interacts with its substrates Help identify human Lon substrates Substrates with effects on central nervous system Identify relationship between CNS substrates and abnormal proteins
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Research Methods E. coli Lon interactions with two substrates –RcsA –SulA Control physiological effects Clear phenotypes
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RcsA –transcriptional activator of capsular polysaccharide genes (mucoidy) lon - lon + RcsA intiates CPS transcription RcsA initiates CPS transcription Lon degrades RcsARcsA not degraded Non-mucoid cellMucoid cell
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SulA SulA (SOS gene) –halts cell division –filament formation Cells exposed to MMS/UV SulA causes filament formation SulA degraded (lon + )SulA not degraded ((lon - ) Filaments resolved into new cellsCell death
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Prior Research RcsA SulA RcsA Competition Hierarchy Proteolytic Binding Site
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Lon Domains 369 679 Ser 411 421 351 ATP Binding Site C-terminus Proteolytic Bindng Site aa residue # 211-271 Met 783 1 N-terminus velcro domain RcsA recognition Site SulA recognition Site?
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Making Mutants Mutagenesis –K11 and Tll strains –Contain antibiotic resistance gene linked to lon –methylating agent: nitrosoguanidine (NTG) –Generation of random point mutations GCATTGCGGGGCTATCGGTCACACTGCATCGTCATCGAATCGGGCGCGCCCTGATTGA CGTAACGCCCCGATAGCCAGTGTGACGTAGCAGTAGCTTAGCCCGCGCGGGACTAACT
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Making Mutants 100/0 45 50 75 Tet r / Kan r 11 minutes 10 minutes lon DNA Packaging –P1vir Lysates –P1vir Bacteriophage –~100 kb (20 genes)
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Making Mutants Transduction –Infection of healthy E. coli with P1vir InfectionRecombination tet r / kan r mutated lon normal lon E.coli P1 vir tet r / kan r mutated lon normal lon P1 vir E.coli
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Making Mutants Requires several phases of screening –1. Selection for mutations on lon Mutant behavior re: RcsA
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Screening for Mutants 100/0 45 50 75 Tet r / Kan r 11 minutes 10 minutes lon Limited DNA capacity
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Screening for Mutants Requires several phases of screening –1. Selection for mutations on lon Mutant behavior re: RcsA –2. Screening using temperature selection
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Temperature Selection Hypothesis Low temperatures Protein folding normal Wild type behavior High temperatures Abnormal protein folding Mutant behavior
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Screening for Mutants Requires several phases of screening –1. Selection for mutations on lon Mutant behavior re: RcsA –2. Screening using temperature selection –3. Screening using temperature selection and MMS Mutant behavior re: SulA
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Mutant Classes I: Lon defective with RcsA Normal cells Mucoid
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Mutant Classes II: Lon defective with SulA Normal Cell Filamentation/ Cell Death On MMS at 42º
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III: Lon defective with RcsA and SulA Mutant Classes Normal cells Mucoid On MMS at 42º Cell Death
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Mutant Classes IV: Lon Gone Wild Normal Cell Cell Death At 42º
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Mutants Isolated 8 Class I Mutants –Lon Defective with RcsA 3 Class II Mutants –Lon Defective with SulA –Intermediate MMS sensitivity 2 Class IV Mutants –Lon Gone Wild –Validates Temperature Selection Hypothesis
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Next Steps Mutant Verification/Identification –Presence of Lon/RcsA/SulA Western Blot –Amplify lon using PCR –Sequence DNA –Compare Mutant Sequence with E. coli lon sequence
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Why Bother? Learn how Lon selects its substrates in E. coli A model for Lon in humans Help identify Lon substrates in humans Understand more about age-related protein misfolding diseases
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Acknowledgements Dr. Janine Trempy Howard Hughes Medical Institute HHMI Selection Committee Undergraduate Research, Innovation, Scholarship and Creativity (URISC) Program URISC Selection Committee
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