Hemoglobin Structure

Download Report

Transcript Hemoglobin Structure

Hemoglobin Structure

Hemoglobin is tetrameric O 2 transport protein found in vertebrate erythrocytes (red blood cells)

»

Hb has changing X

• • • • • •

2 Y 2 composition over life Always has 2 pairs of polypeptide chains Hb A (adult) is

a

2

b

2 [HbA 2 Early Embryo has

z

2

e

2 (2% Hb) is (like

a

and

b

)

a

2

d

2 ] Later Embryo

z

2

e

2

a

and

z

to

a

2

g

2 = Hb F (fetus) have 141 A.A.’s, slightly different

b

,

g

, and

d

have 145 A.A.’s

»

Different oxygen affinities allow passing of O from mother to fetus (more later) 2

X-Ray Crystal Structure

»

23 year project of Max Perutz (1959)

» » » »

4 subunits packed in tetrahedral array One heme/subunit, near surface (25 Å apart)

a

contacts both

b

; no

a

a

or

b

b

contact Hb subunits are similar to Mb

Only 18% of AA’s conserved; same shape

“Globin Fold” common to all vertebrates

• •

Places Heme in correct environment to bind O 2 reversibly Conserve AA’s inclue F8 His and E7 His

Polar/Polar and Nonpolar/Nonpolar subst.

In contrast to myoglobin hemoglobin has 4 °structure

Allosteric Interactions of Hb O

2

Binding

Allosteric Interactions = those between spatially separated parts of a protein

» »

O 2 binding is cooperative O 2 binding is affected by H + , CO 2 vice versa binding and

»

The organic phosphate BPG regulates O 2 binding

Cooperative O 2

»

Saturation Binding of Hb

Y

# occupied sites total # of sites

0

1

»

Mb vs. Hb Y (Oxygen Dissociation Curves)

Y Mb > Y Hb at any pO 2 (partial pressure O 2 )

P 50 = pO 2 at which Y = 50%

Mb P 50 = 1 torr (1 atm = 760 torr)

Hb P 50 = 26 torr

Shapes of the curves

Mb has the shape of hyperbola

K MbO 2 Mb + O 2 K  [Mb][O [MbO 2 2 ] ] Y  [MbO [MbO 2 ]  2 ] [Mb] Y   [O ]  pO Y [O ]  2 [K] pO  2 P • 2 2

Hb has sigmoidal shape

50 K  Hb(O 2 ) n (pO 2 (pO ) n  2 ) ( n P 50 ) n Hb + nO 2  1 Y Y    pO 2 P 50   n

myoglobin 1 SATURATION hemoglobin 0 10 50 o2 O 2 PRESSURE (torr)

»

Hill Plots Tell Us About Cooperativity

Y log  n log pO 2 n log P 50 1 Y log Y 1 Y

Mb n = 1.0

Hb n =2.8

• • Log (pO 2 )

n = Hill Coefficient indicates cooperativity Mb: n = 1.0 = independent O 2 binding

Hb: n = 2.8 = O 2 cooperative binding

Binding the first O 2 makes it easier to bind the next, and so on

Dissociating the first O 2 makes it easier to dissociate the next one

»

Why is Cooperativity good in Hb?

• •

Y changes very rapidly with pO 2 Lung pO 2 = 100torr, Muscle pO 2 = 20 n = 1 then Y lung = 0.79, Y muscle = 0.43 (0.36 delivered) n = 2.8 then Y lung = 0.98, Y muscle = 0.32 (0.66 delivered ) Hb is 1.8 times as efficient as Mb Hb P50 lies between lungs and muscle

H +

»

and CO 2 effects on Hb O 2 Bohr Effect: Increased [H Binding + ] decreases binding

• •

Mb O 2 binding is not affected by [H + ]

Contracting muscle generates H + and CO 2

This helps Hb release O 2 Deoxy-Hb binds H + stronger than oxy-Hb

»

The effect is mutual: high [O 2 ] causes H+ to dissociate from Hb

»

CO 2 effect on Hb binding

Organic Phosphate Regulation of Hb O 2

»

BPG is an organic phosphate binding Concentrations of glycolytic intermediates in erthyrocytes

m

M glucose glucose- 6- P fructose- 6- P fructose- 1,6- P dihydroxyacetone- P glyceraldehyde- 3- P 1,3 bisphosphoglycerate 2,3 bisphosphoglycerate 3 phosphoglycerate 2 phosphoglycerate phosphoenolpyruvate pyruvate lactate 5000 83 14 31 138 19 1 4000 (BPG) 118 30 23 51 2900

From S. Minakami and H. Yoshikawa. Biochem.Biophys.Res.Comm. 18(1965):345. O H C C CH 2 O O O P O O O O P O O

2,3 bisphospho-glycerate (BPG)

BPG Lowers the binding affinity of Hb for O 2

[BPG] = 0, Hb P50 = 1 torr

[BPG] = 4000

m

M, Hb P 50 = 26 torr

Without BPG, Hb couldn’t unload O 2 in cells 1 No BPG SATURATION With BPG 0 10 50 o2 O 2 PRESSURE (torr)

BPG acts by stabilizing deoxyHb

BPG binds by electrostatic interactions to the highly electropositive region (red) in a crevice between the 4 subunits BPG binding site

»

BPG ensures that O 2 peripheral tissues

about 26 fold can be unloaded at the by decreasing the affinity of Hb for O 2

increasing O 2 , on the other hand, promotes the formation of oxyHb whose changed conformation prevents BPG binding because the binding cavity becomes too small

»

Fetal Hb has a lower affinity for 2,3-BPG and therefore has a higher affinity for O 2

BPG regulates O 2 binding between Hb types

This allows transfer of O 2 from mother to child

This explains the need for multiple Hb types

If [BPG] = 0, HbA > HbF for O 2 binding

HbF has neutral Serine in place of HbA His 1 HbF SATURATION HbA O 2 flows from mom to baby !

0 10 50 o2 O 2 PRESSURE (torr)

Structural Basis for Cooperativity

»

Interactions between subunits

• •

A dissociated Hb subunit binds O 2 A

b

4 tetramer binds O 2 like Mb like Mb

Cooperativity must involve subunit interactions

»

OxyHb and DeoxyHb have very different quaternary structures

OxyHb is more compact (

b

Fe —

b

Fe from 40 to 33 Å) changes

When O 2 binds,

a

b

H-bonds are adjusted contacts change as

• •

Electrostatic bonds (Salt Links) also change: OxyHb the CO 2 termini can freely rotate, DeoxyHb CO 2 termini salt linked DeoxyHb has T form (“taut”)

OxyHb has R form (“relaxed”)

»

Changes at the Heme initiate structure switch

DeoxyHb has Fe 0.3

Å out of plane

N Fe

2+

N N N N

N N •

OxyHb has Fe in plane of porphyrin

O O N Fe 2+ N N •

Fe atom pulls the bound F8 His with it

Shifts the whole F helix, EF corner

Salt links are broken at

ab

interface

T-form becomes R-form

R-form has greater O 2 affinity

Cooperativity set in motion

BPG stabilizes deoxyHb T-form by creating more contacts

O 2 binding to Hb causes dissociation of BPG because the cavity gets too small. This favors the R-form as well.

Models for Allosteric Interactions

»

Sequential Model

Only T and R forms possible for each unit

T to R transition of each subunit is induced by O 2 binding, but this does not change the form of other subunits

Conformational changes enhance O 2 binding at the next subunit, but O 2 must bind each subunit before it switches to R

O 2 O 2 O 2 O 2 O 2 O 2 O 2 O 2 O 2 O 2 O 2 O 2 O 2 O 2

O 2 »

Concerted Model

• •

Whole protein changes from T to R form upon initial O 2 binding O 2 has higher affinity for the unbound R subunits

This explains cooperativity

O 2 O 2 O 2 O 2 O 2 O 2 O 2 O 2 O 2 O 2 O 2 O 2 O 2 O 2 O 2 O 2 O 2 O 2 O 2 O 2 »

Actual: mix of the two models. Hb is predominantly T until ~2 O 2 molecules are bound, then it goes all R.

myoglobin 1 SATURATION hemoglobin 0 10 50 o2 O 2 PRESSURE (torr)

Sickle-cell anemia

A Glu normally resides at position 6 of each

b

- subunit. In HbS this amino is mutated to Val

Glu 6

a b b a

Glu 6

the Val for Glu mutation makes deoxy-HbS insoluble -findout why!

Sickle-cell anemia

the Val for Glu mutation makes deoxy HbS insoluble In deoxy-HbS,

b

-subunit residues Phe 85 and Leu 88 reside at the surface and bond with Val 6 on another

b

-subunit. This leads to the formation of long filamentous strands of deoxy-HbS and to the sickling deformation of the erthyrocytes In oxy-HbS,

b

-subunit residues Phe 85 and Leu 88 do not reside at the cell surface, so oxy-HbS does not aggregate. Thus, its oxygen binding capacity and allosteric properties are largely retained.

Hemoglobin

:

a portrait of a soluble protein with 4 ° stucture

A SUMMARY

• • • • • • •

the heme prosthetic group is tightly bound in the protein and is essential for function steric relationships within Hb ensure that the heme group has appropriate reactivity hemoglobin has quaternary structure which gives it unique O 2 binding properties allosterism and cooperativity of binding 2,3-bisphosphoglycerate is a regulatory molecule that stabilizes deoxy-Hb and is essential for the allosterism and cooperativity of binding in Hb there is considerable interplay between the oxygen binding affinity of Hb and [H + ], [CO 2 ] and [2,3-BPG] the interplay between various sites in Hb is mediated through changes in quaternary structure Sickle-cell anemia is an example of a genetically transmitted disease which highlights the effect of one amino acid substitution on protein structure and function