Title: Structure-Function Relationship of Retinal Proteins
1Structure-Function Relationship of Retinal
Proteins
2Structure of Retinal Proteins
C
F
B
A
D
E
G
GPCRs
Retinal proteins or rhodopsins belong to the
superfamily of seven-transmembrane helical (7TM)
proteins. Seven helices, with N-terminus on the
extracellular side and C-terminus on the
cytoplasmic side of the membrane (not necessarily
G-protein coupled)
3Retinal Proteins -- Rhodopsins
- Covalently linked to a lysine
- Usually protonated Schiff base
- all-trans and 11-cis isomers
Chromophore
4Bacteriorhodopsin -- bR
- The simplest ion pump in biology
- The simplest photosynthetic center
- The best characterized membrane protein
- Technological applications in molecular
electronics
- The first membrane protein with a known
atomic-detail 3D structures
5bR role in Bioenergetics
ATP
ADP
ATP Synthase
6Schematic proton path in bacteriorhodopsin
Cytoplasmic side
Transmambrane helices
Transmambrane helices
Extracellular side
7Active Channels Need a Switch Mechanism
H
H
H
hn
H
H
H
H
H
H
H
H
H
H
H
What is the switch in bR? How does it work?
8Photocycle of bR
Photo-induced
5 ms
3 ps
1 ms
5 ms
40 ms
5 ms
All intermediates are trapped in low temperature
and have been characterized by vibrational and
absorption spectroscopy.
9No membrane protein has been studied as
extensively as bR
Photo-induced
5 ms
3 ps
1 ms
5 ms
40 ms
5 ms
All intermediates have also been characterized by
X-ray crystallography!
10Schematic proton path in bacteriorhodopsin
Cytoplasmic side
Transmambrane helices
Transmambrane helices
Extracellular side
11BRs Photocycle
HOOC-D96
bR568
K216
N
H
D85-COO
cytoplasmic
5ms
HOOC-E204
3ps
K603
O645
H
HOOC-D96
HOOC-D96
H
K216
N
N
H
K216
D85-COO
D85-COOH
HOOC-E204
OOC-E204
1ms
5ms
OOC-D96
HOOC-D96
H
K216
N
N
K216
H
D85-COOH
D85-COO
OOC-E204
HOOC-E204
L543
N550
40ms
5ms
HOOC-D96
extracellular
N
light driven proton pump
K216
D85-COOH
M410
OOC-E204
12BRs Photocycle
HOOC-D96
bR568
K216
N
H
D85-COO
5ms
HOOC-E204
3ps
K603
O645
HOOC-D96
HOOC-D96
H
K216
N
N
H
K216
D85-COO
D85-COOH
HOOC-E204
OOC-E204
1ms
5ms
OOC-D96
HOOC-D96
H
K216
N
N
K216
H
D85-COOH
D85-COO
OOC-E204
HOOC-E204
L543
N550
40ms
5ms
HOOC-D96
N
Conformational Change of Helices
K216
D85-COOH
M410
Kuhlbarandt, Nature, 406,569 (2000)
OOC-E204
13Study of bR at three levels
- ?Chromophore
- Analysis of the structure
- Calculation of excited state dynamics
- ?Protein
- Chromophore-protein interaction
- QM-MM calculations
- MD simulation of the photocycle
?bR in the purple membrane Modeling of the
protein in lipid bilayers
14Retinoids
Retinal Schiff base Membrane, covalently bound,
chromophore
Retinoic Acid Nucleus, receptor site, ligand (no
photoactivity)
15Unconventioanl chemistry
The necessity of quantum mechanical treatment of
the chromophore Conjugated p-electronic system,
delocalization The effect of protein matrix on
the ligand
QM is expensive Most of the time, one needs to
use models
16Effect of Conjugation on pKa (Gas Phase Proton
Affinity)
Proton Affinity PA EAH-(EAEH)
17Effect of the methyl groups on pKa
Proton Affinity PA EAH-(EAEH)
No more room for additional methyl groups on the
backbone
18What is the effect of isomerization?
19Isomerization State and Proton Affinity
Proton Affinity PA EAH-(EAEH)
cc B2,B3-di-cis isomer ct B2-s-cis, B3-trans
isomer tc B2-strans, B3-cis isomer tt all-trans
isomer.
Isomerization does not have a strong impact on PA!
20What is the effect of isomerization?
21Retinal binding pocket in bR
Counterion Asp85 Asp212
WATER
22Effect of the environment on PA
Proton Affinity PA EAH-(EAEH)
23In situ isomerization and pKa
24Coupling of electronic excitation and
conformational change in bR
13
7
9
11
15
25Ground and Excited State Potential Energy
Surfaces of Retinal
trans
cis
26Ab Initio QM/MM Excited State MD Simulation
QM
Quantum mechanical (QM) treatment of the
chromophore, and force field (MM) treatment of
the embedding protein
27Isomerization Barriers in retinal
Proton Affinity PA EAH-(EAEH)
Ground state isomerization
Low barriers against double bond isomerization
28A twisted chromophore in bR?
- A twisted chromophore is also experimentally
reported. - X-ray structures of bR report the twisted form of
chromophore - The twist is found around the terminal double
bonds - It may influence pKa of the chromophore