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Determining Structure and Composition of a Model Phospholipid Bilayer ORANGE TEAM Monica Branco Suh Joon Han Matthew Helgeson Kathryn Krycka Jong Keun.

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Presentation on theme: "Determining Structure and Composition of a Model Phospholipid Bilayer ORANGE TEAM Monica Branco Suh Joon Han Matthew Helgeson Kathryn Krycka Jong Keun."— Presentation transcript:

1 Determining Structure and Composition of a Model Phospholipid Bilayer ORANGE TEAM Monica Branco Suh Joon Han Matthew Helgeson Kathryn Krycka Jong Keun Park Chu Xiangiang

2 Phospholipid Bilayers Phospholipid bilayers serve as biomimetic membranes Lipids self-assemble into ordered, multi-layer structure Our system: DMPC –Phospho-choline head group –C 14 hydrocarbon chains

3 Advanced Neutron Diffractometer/Reflectometer Reflection of incident beam based on Bragg diffraction: Slit #2 Slit #1 Slit #3 Slit #4 monitor monocromator sample detector   θ 2θ2θ kiki krkr ktkt QzQz

4 Experiment Objectives Determine quantitative structural information –Bilayer thickness –Bilayer composition profiles –Solvent penetration –Extent of thermal fluctuation

5 Sample Preparation Deposition of lipid solution on glass slide Solvent evaporation Hydration of bilayer film in sample chamber (75% RH) Allow for sample equilibration at 37ºC I(Q) Q (Å -1 ) Glass slide

6 Determination of Bilayer Spacing Phase problem: 100% H 2 O 50/50 H 2 O/D 2 O 100% D 2 O I(Q) Q (Å -1 ) n=1 n=2 n=3 n=4 n=5 Phospholipid bilayer spacing: d = 49.3 Å

7 Solving the Phase Problem Variation of solvent conditions: H 2 O  D 2 O 100% H 2 O 50/50 H 2 O/D 2 O 100% D 2 O I(Q) Q (Å -1 )

8 Scattering Length Density Profiles SLD profiles for lipid C-H chains:

9 Bilayer Composition Determination Selective deuteration of solvent and lipid:

10 Water and Hydrocarbon Profiles Subtraction of profiles allows for identification of species profiles: V CH2 =27 Å 3 V CH3 =54 Å 3

11 Conclusions AND/R allows for detailed, quantitative structural and compositional characterization of biomimetic bilayers –Solving the phase problem –Selective contrast variation Further experiments –Site-specific D-labeling –Protein incorporation


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