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Dodecaborate clusters forms stable pores in lipid membranes

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Presentation on theme: "Dodecaborate clusters forms stable pores in lipid membranes"— Presentation transcript:

1 Dodecaborate clusters forms stable pores in lipid membranes
Melinda Bartok, Lucia Lozano White, Mengxi Wang, Dennis Ledwon and Detlef Gabel 16th ICNCT, June 2014, Helsinki, Finland

2 Why to use Boron clusters?
TEM of tissue from glioma patients after infusion with BSH prior to surgery BSH stained with polyclonal primary Ab and secondary red-fluorescent Ab, Hoechst stained cell nucleus

3 Halogenated boron clusters
B12H122- Zeta potential DSC Cryo-TEM Leakage Toxicity on cells BLM 7.2 Å B12I122- 11.0 Å

4 Zeta potential of 0.5 mM DPPC, DSPC and DPhPC liposomes with dodecaiodo dodecaborate
Binding const.: DPhPC mM DPPC mM DSPC mM

5 Cryo-TEM images of 5mM DPPC liposomes alone and with 50mM B12I122-
200 nm

6 Black lipid membrane technique
Teflon film Bilayer Solvent annulus Electrode Cis Trans Salt solution Monolayer

7 Membrane potential is responsible for pore formation
– 50 mV +100 mV ΔV=150 mV – 100 mV ΔV= – 50 mV 1. Many pores No pores – 50 mV +100 mV ΔV=50 mV – 100 mV ΔV= – 150 mV 2. Many pores No pores – 50 mV +100 mV ΔV=100 mV – 100 mV ΔV= – 100 mV 3. Few pores

8 Interaction of 1μM B12I122- under +100 mV constant potential
Current (pA) Time (s) Current (pA) Time (s)

9 Maximum size of the created pores
5 – 7.30 min const. potential of +100 mV Current (pA) Pore size: 25 Å Current (pA)

10 Interaction of 1μM B12I122- under -100 mV constant potential
Current (pA) Time (s) We also saw that it is concentration dependent-needing concentrations of 1 μM to see pores and sometimes 0,5 μM for transient pores Current (pA) Time (s)

11 Maximum size of the created pores
Current (pA) 7.30 – 10min const. potential of -100 mV Pore size: 45  Å Off-scale pore, we can see how it tries to close, only to open further and then completely close in just 1 milisecond Current (pA) The event goes off scale, but membrane remains stable

12 Interaction of 0.25 μM B12I122- -100mV potential applied in cycles
At lower concentrations Very clear gating Interaction of 0.25 μM B12I mV potential applied in cycles -85pA = 6 Å pore +50pA= 5 Å pore -20pA = 3 Å pore 0 mV - 100 mV 0 mV - 100 mV 0 mV - 100 mV Current (pA) 23 24 25 26 27 Time (min) Interaction of 0.25 μM B12I mV constant potential -400pA = 13 Å pore -700pA= 17 Å pore -450pA = 13 Å pore -250pA = 10 Å pore -350pA = 12 Å pore RIGHT SIDE CYCLES (Attempt 2) // RIGHT SIDE CONSTANT (Attempt 2) Current (pA) 13 14 15 16 17 Time (min)

13 Interaction of B12I122- on decane containing membrane under different potentials
5000 pA 31.5 Å pore -5000 pA 20 25 30 35 40 minutes 1 µM 2 µM 3 µM -100 mV -100 mV -20 mV

14 +cluster +detergent 10 mM HEPES 0.15 M NaCl

15 10 mM HEPES 0.15 M NaCl At 1 M KCl: no leakage!

16 Cooperative pore formation
These clusters stick together 5 clusters care 50 A of length, which is the same size as the DPhPC bilayer (5nm = 50 A) K+ ion sorrounded by 4 water molecules 7- 8 clusters stick together to span the bilayer 5 -6 clusters across to create a big enough pore Leaving a 10 Å diameter pore

17 CONCLUSIONS Holes need potential, concentration and time
Higher concentrations: big holes with short life span Lower concentrations: smaller holes with long life span Average size of holes is around 5-10 Å Holes as big as 45 Å in diameter Closing mechanism much quicker than opening Holes in solvent-containing membranes persist for hour(s) In liposomes, 1 M KCl prevents leakage

18 Thank you for your attention!

19

20 Interaction of 0.1 mM BSH in 0.15 M KCl at -70mV constant potential
Time (s) -200 -400 -600 -800 -1000 -1200 Current (pA) Interaction of 0.1 mM BSH in 0.15 M KCl at -70mV constant potential BSH 0.1 mM 150 mM KCl


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