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Membranes II. Andy Howard Introductory Biochemistry 6 October 2009. Membranes work hard. Transport of various types requires active participation of various proteins and sometimes involves energy input. - PowerPoint PPT Presentation
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10/06/09Biochemistry: Membranes II
Membranes II
Andy HowardIntroductory Biochemistry
6 October 2009
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Membranes work hard
Transport of various types requires active participation of various proteins and sometimes involves energy input.
Interactions between signaling molecules and receptors occurs at the membrane and allow an external signaling molecule to influence internal behavior.
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What we’ll discuss Membrane transport Review Transporting charges
Pores & Channels Passive Transport
Active Transport Moving large molecules
Signal transduction General Principles
G proteins Adenylyl cyclase Inositol-phospholipid signaling pathway
Receptor tyr kinases
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Cartoons of transport types
From accessexcellence.org
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Thermodynamics ofpassive and active transport• If you think of the transport as a chemical reaction Ain Aout or Aout Ain
• It makes sense that the free energy equation would look like this:
• Gtransport = RTln([Ain]/[Aout])
• More complex with charges;see eqns. 9.4 through 9.6.
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Example Suppose [Aout] = 145 mM, [Ain] = 10 mM,T = body temp = 310K
Gtransport = RT ln[Ain]/[Aout]= 8.325 J mol-1K-1 * 310 K * ln(10/145)= -6.9 kJ mol-1
So the energies involved are moderate compared to ATP hydrolysis
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Charged species Charged species give rise to a factor that looks at charge difference as well as chemical potential (~concentration) difference
Most cells export cations so the inside of the cell is usually negatively charged relative to the outside
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Quantitative treatment of charge differences
Membrane potential (in volts J/coul): = in - out
(there’s an extra in eqn. 9.4) Gibbs free energy associated with difference in electrical potential isGe = zFwhere z is the charge being transported and F is Faraday’s constant, 96485 JV-1mol-1
Faraday’s constant is a fancy name for 1.
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Faraday’s constant Relating energy per moleto energy per coulomb:
Energy per mole of charges,e.g. 1 J mol-1, is1 J / (6.022*1023 charges)
Energy per coulomb, e.g, 1 V = 1 J coul-
1, is1 J / (6.241*1018 charges)
1 V / (J mol-1) =(1/(6.241*1018)) / (1/(6.022*1023) = 96485
So F = 96485 J V-1mol-1
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Total free energy change When charges move, we typically have both a chemical potential difference and an electrical potential difference so
Gtransport = RTln([Ain]/[Aout]) + zF
Sometimes these two effects are opposite in sign, but not always
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Pores and channels
Transmembrane proteins with centralpassage for small molecules,possibly charged, to pass through Bacterial: pore. Usually only weakly selective
Eukaryote: channel. Highly selective. Usually the Gtransport is negative so they don’t require external energy sources
Gated channels: Passage can be switched on Highly selective, e.g. v(K+) >> v(Na+)
Rod MacKinnon
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Gated potassium channels Eukaryotic potassium channels are gated, i.e. they exist in open or closed forms
When open, they allow K+ but not Na+ to pass through based on ionic radius (1.33Å vs. 0.95Å)
Some are voltage gated; others are ligand gated
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Protein-facilitated passive transport All involve negative Gtransport
Uniport: one solute across Symport: two solutes, same direction Antiport: two solutes, opposite directions
Proteins that facilitate this are like enzymes in that they speed up reactions that would take place slowly anyhow
These proteins can be inhibited, reversibly or irreversibly
Diagram courtesySaint-Boniface U.
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Kinetics of passive transport Michaelis-Menten saturation kinetics:
v0 = Vmax[S]out/(Ktr + [S]out) We’ll derive that relationship in the enzymatic case in a later chapter
Vmax is velocity achieved with fully saturated transporter
Ktr is analogous to Michaelis constant:it’s the [S]out value for which half-maximal velocity is achieved.
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Velocity versus [S]out
Transport Velocity
0
0.00005
0.0001
0.00015
0.0002
0.00025
0.0003
0.00035
0.0004
0.00045
0.0005
0 0.0005 0.001 0.0015 0.002 0.0025 0.003 0.0035 0.004 0.0045
[S]out
v 0
Vmax = 0.5 mM s-1
Ktr = 0.1 mM
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1/v0 versus 1/[S]outTransport Lineweaver Burk
0
500
1000
1500
2000
2500
3000
3500
4000
4500
-10000 -8000 -6000 -4000 -2000 0 2000 4000 6000 8000 10000
1/[S]out, M-1
1/v0, sM-1
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Primary active transport
Energy source is usually ATP or light Energy source directly contributes to overcoming concentration gradient Bacteriorhodopsin: light energy used to drive protons against concentration and charge gradient to enable ATP production
P-glycoprotein: ATP-driven active transport of many nasties out of the cell
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Secondary active transport Active transport of one solute is coupled to passive transport of another
Net energetics is (just barely) favorable
Generally involves antiport Bacterial lactose influx driven by proton efflux
Sodium gradient often used in animals
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Complex case: Na+/K+
pump Typically [Kin] = 140mM, [Kout] = 5mM,[Nain] = 10 mM, [Naout] = 145mM.
ATP-driven transporter:3 Na+ out for 2 K+ inper molecule of ATP hydrolyzed
3Na out: 3*6.9 kJmol-1,2K in: 2*8.6 kJmol-1
= 37.9 kJ mol-1 needed, ~ one ATP
Diagram courtesy
Steve Cook
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What’s this used for? Sodium gets pumped back in in symport with glucose, driving uphill glucose transport
That’s a separate passive transport protein called GluT1
Diagram courtesy
Steve Cook
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How do we transport big molecules? Proteins and other big molecules often internalized or secreted by endocytosis or exocytosis
Special types of lipid vesicles created for transport
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Receptor-mediated endocytosis Bind macromolecule to specific receptor in plasma membrane
Membrane invaginates, forming a vesicle surrounding the bound molecules (still on the outside)
Vesicle fuses with endosome and a lysozome Inside the lysozyome, the foreign material and the receptor get degraded
… or ligand or receptor or both get recycled
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Example: LDL-cholesterol
Diagram courtesyGwen Childs, U.Arkansas for Medical Sciences
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Exocytosis
Materials to be secreted are enclosed in vesicles by the Golgi apparatus
Vesicles fuse with plasma membrane
Contents released into extracellular space
Diagram courtesy LinkPublishing.com
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Transducing signals Plasma membranes contain receptors that allow the cell to respond to chemical stimuli that can’t cross the membrane
Bacteria can detect chemicals:if something useful comes along,a signal is passed from the receptor to the flagella, enabling the bacterium to swim toward the source
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Multicellular signaling
Hormones, neurotransmitters, growth factors all can travel to target cells and produce receptor signals
Diagram courtesy Science Creative Quarterly, U. British Columbia
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Extracellular Signals
Internal behavior ofcells modulated by external influences
Extracellular signals are called first messengers
7-helical transmembrane proteins with characteristic receptor sites on extracellular side are common, but they’re not the only receptors
Image courtesy CSU Channel Islands
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Internal results of signals Intracellular: heterotrimeric G-proteins are the transducers: they receive signal from receptor, hydrolyze GTP, and emit small molecules called second messengers
Second messengers diffuse to target organelle or portion of cytoplasm
Many signals, many receptors, relatively few second messengers
Often there is amplification involved
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Roles of these systems Response to sensory stimuli Response to hormones Response to growth factors Response to some neurotransmitters Metabolite transport Immune response This stuff gets complicated, because the kinds of signals are so varied!
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G proteins Transducers of external signals into the inside of the cell
These are GTPases (GTP GDP + Pi) GTP-bound protein transduces signalsGDP-bound protein doesn’t
Heterotrimeric proteins; association of and subunits with subunit is disrupted by complexation with hormone-receptor complex, allowing departure of GDP & binding of GTP
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G protein cycle Ternary complex
disrupted by binding of receptor complex
G-GTP interacts with effector enzyme
GTP slowly hydrolyzed away
Then G-GDP reassociates with ,
See fig. 9.39 for details
GDP
GTP
GTP
Inactive
Active
GDP
H2O
Pi
Inactive
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Adenylyl cyclase
cAMP and cGMP: second messengers
Adenylyl cyclase converts ATP to cAMP Integral membrane enzyme; active site faces cytosol
cAMP diffuses from membrane surface through cytosol, activates protein kinase A
Protein Kinase A (PKA) phosphorylates ser,thr in target enzymes;action is reversed by specific phosphatases
Cyclic AMP
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Modulators of cAMP
Caffeine, theophylline inhibit cAMP phosphodiesterase, prolonging cAMP’s stimulatory effects on protein kinase A
Hormones that bind to stimulatory receptors activate adenylyl cyclase, raising cAMP levels
Hormones that bind to inhibitory receptors inhibit adenylyl cyclase activity via receptor interaction with the transducer Gi.
O N
N
N
N
O
caffeine
HN
NNO
N
O
theophylline
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Inositol-Phospholipid Signaling Pathway 2 Second messengers derived
from phosphatidylinositol 4,5-bisphosphate (PIP2)
Ligand binds to specific receptor; signal transduced through G protein called Gq
Active form activates phosphoinositide-specific phospholipase C bound to cytoplasmic face of plasma membrane
O
HO
HO
O
OH
OHPO O-
O
O
O
R1
O
O R2
P
O
O-O
PIP2
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PIP2 chemistry Phospholipase C
hydrolyzes PIP2 to inositol 1,4,5-trisphosphate (IP3) and diacylglycerol
Both of these products are second messengers that transmit the signal into the cell
O
OH
HO
O
O
OH
P
O
-OO-
IP3
P O-O
-O
P
O-
OO-
OH
O
O
R1
O
O R2
diacylglycerol
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IP3 and calcium
IP3 diffuses through cytosol and binds to a calcium channel in the membrane of the endoplasmic reticulum
The calcium channel opens, releasing Ca2+ from lumen of ER into cytosol
Ca2+ is a short-lived 2nd messenger too: it activates Ca2+-dependent protein kinases that catalyze phosphorylation of certain proteins
O
OH
HO
O
O
OH
P
O
-OO-
IP3
P O-O
-O
P
O-
OO-
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Diacylglycerol and protein kinase C
Diacylglycerol stays @ plasma membrane
Protein kinase C (which exists in equilibrium between soluble & peripheral-membrane form) moves to inner face of membrane; it binds transiently and is activated by diacylglycerol and Ca2+
Protein kinase C catalyzes phosphorylation of several proteins
OH
O
O
R1
O
O R2
diacylglycerol
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Control of inositol-phospholipid pathway After GTP hydrolysis, Gq is inactive so I no longer stimulates Plase C
Activities of 2nd messengers are transient IP3 rapidly hydrolyzed to other things Diacylglycerol is phosphorylated to form phosphatidate
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Spingolipids give rise to 2nd messengers Some signals activate hydrolases that convert sphingomyelin to: sphingosine sphingosine-1-P, and ceramide
Each of these modulates a second messenger
QuickTime™ and aTIFF (Uncompressed) decompressor
are needed to see this picture.
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Fates of the three sphingolipid products Sphingosine inhibits Protein Kinase C
Ceramides activate a protein kinase and a protein phosphatase
Sphingosine-1-P can activate Phospholipase D, which catalyzes hydrolysis of phosphatidylcholine;products are 2nd messengers
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Receptor tyrosine kinases
Most growth factors function via a pathway that involves these enzymes
In absence of ligand, 2 nearby tyr kinase molecules are separated
Upon substrate binding they come together, form a dimer
exterior
interior
ligands
Tyr kinase monomers
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Autophosphorylation of the dimer
Enzyme catalyzes phosphorylation of specific tyr residues in the kinase itself; so this is autophosphorylation
Once it’s phosphorylated, it’s activated and can phosphorylate various cytosolic proteins, starting a cascade of events
PP
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Insulin receptor
Insulin binds to an 22 tetramer;binding brings subunits together
Each tyr kinase () subunit phosphorylates the other one
The activated tetramer can phosphorylate cytosolic proteins involved in metabolite regulation
Sketch courtesy ofDavidson College, NC