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Encapsulation for Drug Delivery
7th August iGEM Team 2009 Charles Dave Dineka James Kun Nuri Royah Tianyi
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The Project “Auto-encapsulation of protein drugs for release in the small intestine.”
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Gantt Chart ACTIVITIES Week 4 Week 5 Week 6 Week 7 Week 8 Week 9
MIT Project description Assay Protocols Cloning strategy Genetic Circuits Biobricks Genes to PCR Wet lab plan Gantt Chart Dry lab plan Order genes Order Biobricks Start Wet Lab PCR & Test Promoters Timer + M1 integration M2 M3 Start Dry Lab Genes delivered Biobricks delivered Complete In progress To do Unknown
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Modules 1 & 2: Update
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M1 - Hunt for Cellulase No clone readily available. Professor input?
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M2 - Sodium Acetate Food grade RAPID inducible crystallisation
Exothermic Dissolves under acidic conditions
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The Timer Module Integration
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Timer Design Rules 1. Try rely on activation, not repression. (Problem with degradation rates.) 2. Inputs must accumulate over time to see delays. 3. Last promoter must be as “non-leaky” as possible. 4. Tunability - linked to inducible promotor.
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Timer - Logic A PoPS (Encapsulation) AB B Inducible Constitutive
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Tunability LuxI M2 Lux R + I PoPS LuxR Start Timer – v1 PBAD PLux X
Kirsten’s favourite Tunability PBAD PLux LuxI M2 Lux R + I PoPS (Encapsulation) X LuxR Start
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! PAH or Cellulase LuxR LuxI Encapsulation (M2) genes PBAD PluxR X M1
Conflict between: Start of experiment Threshold setting X PBAD LuxI LuxR Timer M2 PluxR Encapsulation (M2) genes
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! PAH or Cellulase LuxR LuxI Encapsulation (M2) genes PBAD PluxR
Conflict between: Start of experiment Threshold setting PBAD LuxI J23114 LuxR Timer PluxR Encapsulation (M2) genes M2
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X Anti-LuxI LuxI M2 Lux R + I PoPS LuxR Timer – v2 PBAD PLux J23114
Bba_K145013 Anti-LuxI PBAD PLux LuxI M2 Lux R + I PoPS (Encapsulation) J23114 LuxR
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Tunability of IPTG in lacY-strains
Induction of lac-regulated promoter in lacY- and lacY+ strains, from Jensen et al. Eur.J.Biochem, 211, (1993)
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PluxR Output
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PTET Lactonase luxI tetR M2 PoPS LuxR Timer – v4 PLAC PLux Lux R + I
Td (lactonase) =4.7hrs PTET Lactonase Bba_C0060 Ts (TetR) PLAC PLux luxI tetR M2 Ts (LuxI) Lux R + I PoPS (Encapsulation) J23114 LuxR
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Dry Lab Preparation
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Dry Lab So far… Designed & ordered primers
Designed TaqI, DpnII & cI BBs Testing construct design Clones ordered (Kirsten) Started step-by-step protocols & shopping list Next week… Place MrGene order SLIC preparation Complete step-by-step protocols & shopping list
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BioBricks Remaining… Promoter = Repressible (lambda cI) M3 Part
BBa_K [Harvard ‘08] Part Obtain by… Diagram CI (temperature sensitive) Synthesise? / PCR? Promoter = Repressible (lambda cI) Synthesise (different sequence) Registry
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Wet Lab Parts, Testing & Progress
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So Far… Competent cells – 4 x 10^6 cells/ug DNA 0 contaminants
No native resistance
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So Far… Registry - 8 taken out
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Next week… Registry – extract timer BBs
Start PCR – M1 (2), M2 (5) & M3 (1) Start to characterise promoters (Jason Kelly) Organise teams (1 bioscientist, 1 bioengineer) - team 1 = PCR - team 2 = promoter testing
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Summary - Checklist Weekly 5 Aims: Trade name Assay Protocols
Cloning Strategies Finalise genetic circuit Order BioBricks Primer design Wet lab plan
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Summary - Checklist Week 6 Aims: Place MrGene Order (Wednesday)
Assay Protocols (Monday) Cloning Strategies (Monday) Wet lab – PCR & test promoters & extract BBs Dry lab tutorial
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Any questions?
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Timer – v3 (Lock/Key system)
PtetR Bba_K145300 J23109 Lactonase LVA BBa_K145102 Lock + Key PLux J23114 LuxI M2 Lux R + I PoPS (Encapsulation) J23114 LuxR
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