Further Studies of the Isomerization of Bovine Plasma Albumin. The

Neal C. Robinson and Charles Tanford. Biochemistry 1975 14 (2), 369-378 ... Kamala Kant Vijai and Joseph F. Foster. Biochemistry 1967 6 (4), 1152-1159...
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ISOMERIZATION OF BOVINEPLASMA ALBUMIN [CONTRIBUTIOK FROM

THE

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DEPARTMENT O F CHEMISTRY, P U R D U E USIVERSITY]

Further Studies of the Isomerization of Bovine Plasma Albumin. The Effect of Detergent Ions at Low pH and Preliminary Observations at High pH1 BY JOSEPH F. FOSTER AND KOICHIRO AOKI~ RECEIVEDMAY12, 19-58 The isonierization (X-F) equilibrium of bovine plasma albumin was studied in the presence of sodium dodecyl sulfate (SDS) a t pH values below the isoelectric pH. This detergent has a pronounced effect in displacing the equilibrium toward the native (K) form. The pH dependence corresponds to the uptake of three hydrogen ions in the conversion of N to F as was previously found in absence of detergent, The dependence of composition on detergent ion concentration can be fitted most accurately by assuming t h a t the S form possesses 10 strong binding sites of intrinsic dissociation constant 7.5 X whereas in the F form these sites are destroyed and replaced by 100 weaker binding sites of intrinsic constant 2.7 X lo-'. This change in binding behavior corresponds very closely to that previously deduced by Pallansch and Briggs to explain the all-or-none binding of SDS by plasma albumin a t alkaline pH. It is concluded t h a t the K-F transition is responsible for such cofperative detergent binding, Over most of the binding range electrophoretic mobilities of both forms were independent of detergent concentration indicating detergent binding under these conditions to be competitive with chloride binding. T h e cationic detergents dodecyltrimethylanimonium bromide and dodecglpyridinium bromide were found to be without appreciable effect on the N-F equilibrium under the conditions employed. Some preliminary studies are reported which indicate the S-F transition to occur in absence of detergent at pH values above 10. Under such conditions, however. the transformation appears not to be completely reversed on lowering the pH.

In previous studies in this Laboratory it has been shown that bovine plasma albumin (BPA) undergoes an "isomerization" equilibrium in the pH range 3.5-4.5 in presence of chloride It has also been found that this equilibrium is influenced by the species of anions coexisting in the system. Thus the position of the equilibrium is shifted in the acid direction in the order SCN- > C1- > acetate, this sequence being the same as the order of relative binding affinities of the anions. I t was thought of interest to study the effect of the strongly bound detergent ions on the equilibrium. In this study the effect of sodium dodecyl sulfate (SDS), which is one of the most commonly employed detergent anions in protein studies, has been examined. Limited studies have been conducted with cationic detergents dodecyltrimethylammonium bromide (DTAB) and dodecylpyridinium bromide (DPB). This study seemed of particular importance in view of the repeated observations showing the cooperative nature of protein-detergent binding. 4--8 Thus it would be of great interest if i t could be shown that the N-F isoinerization were responsible for cobperative bincling. The results indicate strongly that this is the case.

Experimental Pentex bovine plasma albumin, Lot KO.A1201, was used. Protein solutions were de-ionized by means of the Dintzis ion-exchange c01umn.~ Protein concentrations were determined in a Beckman Model D U spectrophotometer assuming a value of E:,",. of 6.67 at 279 mp. 411 reagents ( 1 ) This investigation was supported in p a r t by t h e National Cancer Institute, National Institutes of Health, Grant (2-2248, a n d t h e National Science Foundation, Grant G-1953. Presented in p a r t before t h e division of Biological Chemistry, American Chemical Society, April, 1958. ( 2 ) Chemistry Laboratory, Kagoya City University, Mizuho-ku. Nagoya, Japan. (3) K.Aoki and J. 1;. Poster, THIS J O U R N A I . , 78, 3538 (10813);79, 3385, 9393 (1957); J . I'. lpostcr and K. Aoki, J . Z'hys. C h e m . . 61, 1309 ( I9.57). (4) IT. P. I,iindgrcn, 7"is J O C R N A I . ,63, 28.54 (1911). (5) F. W. I'utnani and €1. S e u r a t h , J. B i d . Chem., 169, 195 (11315). ( 6 ) (a) J. T. Yang a n d J. F. Foster, THISJOURNAL, 76, 5560 (1053) ; (b) J. F. Foster and J. T. Yang, ibid., 76, 1015 (1954). (7) hI. J. Pallansch and D. R . Brlggs, i h i d . , 7 6 , 1396 (1954). ( 3 ) R. .40ki snrl J. IIori, R!dI. Chrne. S u r . J a p a n , 29, 104 (l0:fi) ( 9 ) 1-1 \I I l i n t v i i , l'h U . 'l'lit1qis, 1121rviird T l n i v e r < i t y , 1452.

were of C.P. grade. The S D S had been synthesized prcviously.10 The cationic detergents dodecyltrimethylammonium bromide (DTAB) and dodecylpyridinium bromide (DPB) also were synthesized." Cellophane bags for dialysis were boiled in sodium carbonate solution prior to use. Electrophoresis of BPA in presence of SDS was carried out at ionic strength 0.02 chloride ion and at 0" using a Perkin-Elmer electrophoresis apparatus Model 38 equipped with Schlieren scanning optical system. Sedirneiitdtion measurements were conducted at room temperature (2330") at 59780 r.p.m. using a Spinco Model E. ultracentrifuge equipped with phase-plate Schlieren optical system. I n preparing electrophoresis solutions 9 cc. of protein solution was dialyzed overnight against 391 cc. of a mixture of HCl and iYaC1 in a cold room a t 1-2" using mechanical agitation. On the following d a y the SDS solution of desired concentration was made up using 10 ml. of the outer solution from the dialysis. One ml. of this detergent solution was added to the protein solution to yield 10 1111.of protein solution of the desired protein and detergent concentration. After adding the detergent the protein solution was again permitted to stand overnight in tlie cold room. I n all studies the BPX concentration was held constant at 0.2% (20 mg. in 10 ml.) and that of SDS TWS varied from 0 to 10 mg./lO ml. In this procedure no detergent was added t o the supporting electrolyte. In earlier experimentswhere detergentwas added to thesupportirig electrolyte difficulties were encountered in the form of lack of enantiography in the electrophoresis patterns. It is fell that this probably resulted from incomplete equilibration of detergent across the dialysis membrane. I n some cases a t high detergent concentration there was even a n appearance of precipitate in the ascending limb. It is calculated below t h a t the free detergent concentratiori in the protcin solutions was of the order of 10-6 to 10-j molar. Hence omission of detergent from the supporting electrolyte seems justifiable. The pH of protein solutions was measured using ;L Beckman Model G pH meter, just prior t o electrophoresis, at room temperature. The conductivity, however, was measured at 0'. Mobility values reported are mean values obtained from ascending and descending patterns. Pcr cent. compositions were calculated from ascending patterns only.

Results Some typical electrophoretic pattcrris arc reproduced in Fig. 1. It is seen that eiiantiogtxlhy is reasonably good i i i most cases. I n Fig. 2 is showit thc cffect of variation of total detergent c(mcciitr:ition on the percentage cornposition of the systcin a t a single PH, 3.91, ionic strength 0.02. T h e (10) K. Aoki, H. Shimosato and Y. Kamino, B d l . K a ~ o y nC i t y r ' u i u . , 1, G7 (1955). (I I) K A u k i , 11, I w p i i l > l i < l i w l

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JOSEPH

VOl. 80

F. FOSTER AND KOICHIRO AWI

on 3.59

A

- 6

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L

D k 4 -

-

ACG

DECG

Fig. 1.-Electrophoretic patterns of BPA in presence of SDSat0.02C1-,O0d6.0voItcm.-~: A,pH3.59,BPA/ SDS = 20/0.1,8OoO sec.; B, #H3.78, BPA/SDS = 20/0.1. 8000 sec.; C, pH 3.92, BPA/SDS = 20/0.1, 6000 w.; D. pH 4.19, BPA/SDS = U)/O.l, 6000 se.;E, pH 3.93 BPA/SDS = 20/0,6000 sec.; F. pH 3.93, BPA/SDS = 20/0.2, 6000 sec.; G, pH 3.90 BPA/SDS = 20/0.3, 6000 sec.; H, pH 3.91, BPAISDS = 20/0.6,6000 sec.

0 0

0.50

1.00MG.

AMOUNT OF SDS.

Fig. 3.-Mobility values us. amount of SDS added to 20 mg. of BPA; pH 3.91 i 0.02; 0.02 M C1- at . ' 0

tained without SDS which are seen to be in agreement with the data found A few measurements wefe made in the presence of acetate (0.02 a t PH 4.08 with variation of SDS concentration. The r e d t s were in essential agreement with those in chloride and also indicated the mobilities of the two forms to be independent of@DS concentration. The cationic detergents DTAB and DTB were found to be without appreciable effect on the distribution of N and F forms up to concentrations of even 1 mg./20 rng. protein. In one experiment with 2 mg. DTAB quantitative interpretation was precluded by slight convective disturbances. A few sedimentation velocity measurements were made to check on the possible alteration of the frictional properties of the protein by detergent and by high PH. At pH 4.0 in presence of 1 mg. of SDS to 20 mg. of protein a single sedimenting boundary was obtained with normal sedimentation coefficient (Sao,,, 4.5 svedbergs). At PH 10.5 and 10.8 values of 3.2 and 2.2, respectively, were noted.

M>

.

idy 11

u tt 0 1 " 0

1

I

I

I

1

0.50

1

1

1

'

1

1.00 MG.

AMOUNT OF SDS.

Fig. 2.-Per cent. N form us. amount of SDS added to 20 mg. of BPA; pH 3.91 i 0.02; 0.02 M C1- at . ' 0

Discussion equilibrium clearly shifts toward the N form with The distance migrated by both N and F boundincreasing detergent concentration. Above 0.5 mg. SDS per 20 mg. protein only N form exists in meas- aries, both in the ascending and descending limbs urable concentration a t this pH. of the electrophoresis cell, was in all cases strictly In Fig. 3 are shown mobilities of the two com- proportional to the elapsed time of electrophoresis. ponents as a function of the amount of SDS added. This together with the reasonably high degree of Somewhat surprisingly the mobilities of both enantiography obtained again indicates the abforms are found to be constant regardless of SDS sence of re-equilibration effects which might inconcentration so long as both forms exist in rneas- validate interpretation of the boundaries, as we urable concentration. In the region where the N recently have pointed out.'* form alone exists the mobility appears to decrease The shift toward more acid values of the midsign3cantly with increasing detergent concentra- poinr of the N-F equilibrium in presence of the tion. However, it should be pointed out that strongly bound anion SDS is in accord with the mobilities were somewhat less reproducible at the previous finding that this shift parallels in all higher SDS concentrations. cases the relative binding ailinity of anions. Figure 4 shows the effect of PH on the N-F Previous studies of the interaction of SDS with equilibrium in the presence of a constant concen- proteins have been confined almost entirely to the tration of SDS, 0.1 mg. per 20 mg. protein. At &line side of the protein isoelectric point. this small concentration the SDS is seen to have Putnam and Neurathl* observed that acid to the an appreciable effect on the position of the equi(12) J. F. Foster and K. Aoki, Tma JOURNAL, 80, 1117 (1968). librium. To this figure are added new data ob(13) F. W. Putnam and H. Neurath. ibid., 86, 692 (1944).

ISOMERIZATION OF BOVINEPLASMA ALBUMIN

Oct. 5, 1958

Fig. 4.-Per

cent. composition os. pH, 0.02 M

C1- a t 0":

8, % ' N form when 0.1 mg. SDS was added to 20 mg. BPA;

0, % ' N form without SDS, new data. The curve drawn is from previously published data.*

isoelectric point a precipitate is generally obtained when SDS and horse serum albumin are mixed. It was observed, however, that when the protein is in relatively large excess no precipitate results. Similar experiments were performed by one of the authors.8 When the weight mixing ratio horse serum albumin/SDS was between 100/0 and approximately 95/5 there was no precipitate. All of the present studies with SDS were within this range and no precipitation took place. It should further be emphasized that the free detergent concentration was of the order lo4 molar as compared to the critical micelle concentration (c.m.c.) value of about 0.0035 at 0.02 ionic strength.8r10 It is clear that the possible participation of detergent micelles in the reaction need not be considered. The cooperative nature of the binding of detergent ions by globular proteins was first clearly shown by L ~ n d g r e n . ~Putnam and Neurath5 showed that in the interaction of horse serum albumin with SDS two discrete protein complexes are formed, PDn and PDzn, where n is approximately 55. Yang and Foster,6a using dodecylbenzenesulfonate and BPA, showed that there is first a statistical reaction, detergent ions being bound one by one up to a binding limit of approximate 12. As this binding limit is approached there is a complete change in the nature of the reaction and approximately 3 5 4 0 additional detergent ions are taken up cooperatively to yield the complex PD,. Essentially the same conclusion was reached by Pallansch and Briggs' using BPA and SDS. They concluded that 10 sites are available for the initial statistical reaction and 80 for the second. Especially clear evidence for the three discrete complexes, PD12, PD, and PD2, has been noted recently. l 4 These results indicate rather clearly that relatively few, perhaps 10 or 12, strong binding sites exist on the native albumin molecule and that ad(14) K. Aoki, t o be published.

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ditional binding sites are exposed through some cooperative structural change which takes place as saturation of the original sites is approached. At the time of initiation of the present studies it was postulated that this coaperative reaction might be identical with the N-F transformation. The fact that cooperative interaction with cationic detergents does not take place a t low pH, as has been shown,6b thus would be explainable readily since under such conditions the F form would pre-exist in absence of detergent. It might be postulated that the conversion of W to F takes place a t high pH as well as low. Tanford, et a1.,16 have shown expansion of the BPA molecule to take place above p H 10. If it is true, as we have s ~ g g e s t e d that , ~ conversion of N form to F is a necessary prerequisite to expansion this should indeed be true. A few preliminary electrophoresis experiments have been carried out above $H 9 which indicate isomerization to take place. Using 0.27, protein in carbonate buffers of ionic strength 0.02 a single boundary was obtained a t p H 9.8. At pH 10.2 a small percentage of a slower moving boundary appeared16 and with increase in pH the proportion of this form increased.17 A pattern a t pH 10.8 is reproduced in Fig. 5. Enantiography is clearly not as good as in the low pH studies.

p H 10.8 WOMA.

L 7000 SEC*, L

-

--

ACG DECC Fig. 5.-Electrophoretic pattern obtained on BPA at the $14 and ionic strength indicated, carbonate buffer.

A detailed analysis of the effect of SDS on the N-F equilibrium is rendered difficult by our lack of detergent binding data under the conditions used. Obtaining such data of sufficient precision a t the very low detergent concentrations employed appears to be out of the question by conventional techniques and would probably best be accoillplished by means of radioactive SDS. Hon-ever, some enlightening calculations are possible T\ ithout such data. The fact that N combines more strongly with SDS than does F seems clear from the direction rif the shift in the equilibrium. The free dctergeiit concentration (D) is given by ( D )= (Do) - YN(N)- YF(F)E (no) = r h ( S 1 since Y F -corrected it would be ap~iroxi~nately 3 X 1W6. Iluu-ever, this dews niit secm to seriously 3Ilvcdid:ite t l ~ rCriieriiI (.or1 clusion reached. (23) P. 1,. 13nycr. 1'. l , , i r n , ( ~ , ,Halluii rid 1 \ I , I id,. I . Ei,.i C1)t.i h i s\ i.. . 162, 1 162, 1S1 ( 1 0 I F i ) ; I ' 13. 13oyer. G. H,iIloii ani1 J . h l . I I ~ L ,i ~ ( IS4Cj).

(24) Evidence t h a t this stabilization is only apparent and due t r r repression of aggregation has been presented recently by Loseva and Tsyperovich.2s J t seem? likely, however, thp.t the r r w t i i ril:d a n d n o t limitr,l to ic.iirei>iggregntir,n f2..,) 4

I . . I . ( r i e %ori.1 ~

S

'l'sypt.r,gt ~ c h f'd/oi,! , .I. 19,

Oct. 5, 1958 I

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ISOMERIZATION O F BOVINE I

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P L A S M A ALBUMIN

I

"'; -2

- 3 t , 10 20 [DO]X lo5. Fig. B.-Plots of log K - log K' oerszrs total detergent coilcentration. Circles are experimental points. Curves drawn are theoretical. Curve A, K N = 7.5 X curve B, K N = 5 X l P 5 ; curve C, K N = 7.5 X KF = 2.7 X m = 100. In all cases n = 10. 0

I

I

I

I

I

I

I

I

-I

0

5 10 [D] X lo6. Fig. 7.--Theoretical plot of log K - log K' z'ersus free detergent activity showing reversal in the direction of t h e shift of the equiiibriunl at high detergent concentration.

anion uptake. In studies of dye binding i t also has been found that the increase in mobility with bindagents it seems probable that the effect of anions is ing corresponds to only 0.33 to 0.4 that exto shift the N-F equilibrium toward the native or pected. 2 7 ~ 2 8 These last mentioned results indicate N form. At similar concentrations with deter- that in many cases detergent or dye binding is comgent ions the Pi form would already be saturated petitive with the binding of other anions. Klotz, with anion and the effect would be strongly in the et U Z . , ~ ~have shown competitive binding of deterreverse direction. gent and methyl orange to plasma albumin. Interpretation of the electrophoretic mobilities The present studies are striking in that experiraises some puzzling problems. It was previously mentally no change in mobility results from SDS calculated3 using Henry's equations with appro- binding over most of the range of detergent conpriate corrections for molecular asymmetry that centrations studied. This indicates an extreme for BPX a t 0.02 ionic strength and 0" the ratio competition, one chloride ion being ejected for each net charge to electrophoretic mobility would be SDS anion bound.30 Why a decrease in mobility 2.7 X I @ . The mobility increment A p / A Z cor- of the N form should set in after the disappearance responding to this value would be 0.37 X lop5. of the F form is not clear. The implication is that This relation appeared to be highly satisfactory in not all of the SDS binding sites are occupied by interpreting our previous data in absence of deter- chloride ions and those so occupied are first ocgent.26 cupied by detergent. This clearly suggests that I n their electrophoretic study of the system not all of the assumed 10 or 12 sites are equivalent. BPA-SDS a t pH 6.8 Pallansch and Briggs7 found a In conclusion i t is a pleasuie to acknowledge the linear relationship between mobility and r in the interest and helpful suggestions of Dr. I f . Laskowfirst statistical binding range ( r < 10). The slope ski, Jr. corresponded to Ap!& = 0.27 X lop5 a t 0.2 ionic INDIANA strength and 20". The calculated value of Ap/AZ LAFAYETTE, under these conditions is 0.31 X indicating an ( 2 8 ) R. Smith and D. K. Briggs, ibrd., 54, 33 (19.50). (29) I. Klotz, H. Triwush and I;. Walker, THISJ O U R N A L , 70, 2935 increase of one net negative charge per SDS anion bound. On the other hand using dodecylbenzene- (1918). (30) Alternatively, of course, it could be postulated t h a t SDS bindsulfonate and BPA Yang and Foste$ found a ing is accompanied by uptake of protons. This seems much less relatively small increase in mobility in the first likely. It is worthy of note t h a t t h e difference in mobilities between binding region indicating the charge to increase N and I' corresponds almost exactly t o three net charge units over the entire range in which they coexist in measurable quantity. T h e much less than proportionately with the increased hydrogen ion dependence of t h e equilibrium also indicates a diflerence (26) T h e corresponding calculated values of A d A Z a t 0.10 and 0.20 ionic strength and a t 0' are 0.22 and 0.175 X respectively. These values appear t o be in good accord with other results in t h e literature, for example those of Longsworth and Jacobsen.27 ( 2 7 ) L. G. Longsworth and C. F . Jacobsen, J. Phys. Colloid Chem., 63, 126 (1949).

in binding of three protons. A difference in mobility corresponding t o three charge units was found also in our earlier studies.2 Competitive binding must be assumed for both forms since binding t o F is not negligible. It is calculated, using t h e binding constants deduced above, t h a t IF = 4 and Y N = 5.7 a t t h e highest SDS concentration where F is observed, ;.e., a t 0.4 mg. SDS/20 mg. protein.