A DIFFERENTIAL ULTRACENTRIFUGE TECHNIQUE FOR

May 1, 2002 - E. Glen Richards, and H. K. Schachman. J. Am. Chem. Soc. , 1957, 79 (19), ... L. W. Nichol and A. B. Roy. Biochemistry 1966 5 (4), 1379-...
0 downloads 0 Views 278KB Size
5324

COMMUNICATIONS TO THE EDITOR

Vol. 79

pathway of the biochemical conversion of choles- possible to perform differential experiments terol t o hydrocortisone, cholester01-2I-'~C was whereby very small changes in sedimentation coprepared4 and gave, on incubation with bovine efficients can be measured accurately. This comadrenal gland tissue, h y d r o c ~ r t i s o n e - ~ .5 ~ C h part munication deals with such experiments and some of the isolated h y d r o c ~ r t i s o n e - ~ ~(5.15 C mg.; potential applications. specific activity, 159 d.p.m./mg.) was diluted with The technique involves a comparison, a t conan equal amount of non-labeled hydrocortisone, jugate levels, of the refractive indices of two soluand then degraded by periodate oxidation according tions contained in separate compartments of a to a procedure previously employed for similar double-sector ultracentrifuge cell. If both solureactions.6 From the oxidation mixture, 7.5 mg. tions are identical the Rayleigh pattern consists of of neutral material was recovered and was found a series of parallel, straight interference fringes. t o contain no hydrocortisone after paper chroma- For the fringes to be straight even in the presence tographic analysis. From the acidic fraction of concentration gradients, the two boundaries (9.7 mg.), 1lp, 17a-dihydroxy-3-oxo-4-etiocholenicmust migrate and spread a t the same rate so that acid7 was isolated and identified by comparison the refractive index difference a t conjugate levels with an authentic sample, by mixed paper chroma- throughout the cell is constant. When one boundtography,s and by its ultraviolet absorption spec- ary moves faster than the other, the fringe pattern trum in concentrated sulfuric a c d g This etio a t the boundaries is warped to produce curved acid was found t o contain no radioactivity.'O fringes whose shape resembles the tracings proCarbon atom 21 of the hydocortisone-lK! was duced by schlieren optical systems. Depending obtained as formaldehyde which was isolated as upon which compartment contains the faster its dimedone derivative, 4.6 mg., m.p. 191.5-102°. moving species, the pattern will show a maximum A mixture of this derivative and an authentic or a minimum. n'ith transport equations the reference sample (m.p. 192-193') melted a t 191.3- difference in sedimentation coefficients can be 192' (melting points not corrected). The dime- expressed directly in terms of the change with time done derivative had a radioactivity'O of 2G of the first moment of the area defined by the curved d.p.m./mg.ll fringes. This evidence demonstrates that carbon atom 21 T o rest the method small amounts of DnO were of cholesterol is maintained during the biochemical added to different solutions of bushy stunt virus, conversion of cholesterol to hydrocortisone and that and the reduction in sedimentation coefficient of the biosynthesis of hydrocortisone from cholesterol the virus was measured by the differential techin the adrenal cortex involves the elimination of nique. For decreases of O.82YO and l,65y0 (detercarbon atoms 22-27 of the original cholesterol side mined by interpalation of data from conventional chain. ultracentrifuge gives 0.7SYO and 1.61YO, respec(4) P. Kurath and M. Capezzuto, THIS JOURNAL, 78, 3527 (195G). tively. Comparable precision is realized in experi( 5 ) F. M. Ganis, P. Kurath and &I. Radakovich, F e d e r d i o i t Proc., ments with proteins. 16, 357 (1957). The sensitivity and accuracy of the method even (6) S. A. Simpson, J. F. Tait, A. Wettstein, R. PJeher, J. v. Euw, a t this early stage of development are sufficient 0. Scbindler and T. Reichstein, H e l v . Chim. Acta, 37, 1200 (1954). (7) J. v. Euw and T. Reichstein, ;bid,, 26, 988 (1942); H. L. hlason, to commend it for many experiments involving W.31.Hoehn and E. C. Kendall, J. Biol. Chem., 124, 459 (1938). small differences in sedimentation coefficients. (8) A. Zaffaroni and R. B. Burton, ibid., 193, 749 (1951). These changes may result from reduction in the (9) A. Zaffaroni, THISJOURNAL, 72, 3828 (1950). buoyancy term as with DzO or from a change in the (10) Radioactivity determinations by New England Nuclear Corporation, Boston, Massachusetts. molecular weight or frictional coefficient of the (11) The amount of the dimedone derivative obtained was in excess macromolecule. The latter is illustrated by preof the expected amount and the radioactivity of the sample was lower liminary results from a study of the binding of than the calculatedvalueof 98 d.p.m./mg. However, it was found that small ions to serum albumin, in which the sedimenthe elution of two filter paper blanks yielded 23.2 and 34.3 mg. of residue which gave upon analogous periodate oxidations and reaction with tation coefficient decreased by about 0.5y0despite dimedone, 2.4 and 3.5 mg. respectively of the dimedone derivative of an increase of 4YO in molecular weight. The techformaldehyde. This would account for t h e lower radioactivity obnique also provides valuable data for the analysis tained in the experimental sample. of equilibrium systems involving rapid reactions DEPARTMENTS OF SURGERY RESEARCH) P. KURATH between a small ion, A, and a protein, P, to form (DIVISIONOF CANCER AND BIOCHEMISTRY, UNIVERSITY OF F. M. GAXIS complexes, PAi, with i varying from 0 to n. For ROCHESTER MEDICALCENTER M. RADAKOVICHsuch systems equation (1) gives the equilibriuni 20, NEW PORK ROCHESTER concentration of free A component RECEIVED AUGUST 5 , 1957

A DIFFERENTIAL ULTRACENTRIFUGE TECHNIQUE FOR MEASURING SMALL CHANGES I N SEDIMENTATION COEFFICIENTS'

( 1 ~

[A]and [?I

are the total concentrations and SA and

Sir:

sp are the sedimentation coefficients of the pure

With the recent adaptation of the Rayleigh interferometer to the ultracentrifuge,* i t has become

components, and SA and Sp are the constituent

(1) This work has been supported in part by a grant from the National Science Foundation. (2) This optical system is available commercially from the Spinco Division, Beckman Instruments, Inc., Palo Alto. California.

(3) Svenssona obtained similar fringe patterns with the Rayleigh interferometer during examination of two identical diffusing boundaries which were slightly displaced from one another. (4) H. Svensson, Acta Cheiit Scnnd , 3, 1170 (1049). ( 5 ) H.K. Schachman. in preparation.

COMMUNICATIONS TO THE EDITOR

Oct. 5, 1957 sedimentation coeficients

(s

= Caisi

where

ai

i:o

. ) Different methods can be used t o evaluate SA.^

TABLE I REQUIREMENT FOR “ACTIVE CERAMIDE“

5325 I N SPHINGOMYELIN

SYNTHESIS

is the weight fraction appearing as the ithspecies

Additions

Sphingomyelin synthesized, millimicromoles

Sphingosine 0 N-Acet yldihydrosphingosine 1 N-Acetylphytosphingosine6 1 “Active cerarnide” (mixture of K-acetylsphingosine isomers) 85 IY-Acetylsphingosine derived from recryst a l k e d triacetyl~phingosine~ 17 (6) du Pont Fellow in Biochemistry. This work is submitted in IY-Acetylsphingosine after treatment with partial fulfillment of the requirements for the Ph.D. degree in Bioacetic-sulfuric acid 155 chemistry at the University of California. Each tube contained 50 pmoles of Tris buffer, PH 7.4, 20 BIOCHEMISTRY DEPARTMENT ASD VIRUSLABORATORY OF CALIFORNIA E. GLENRICHARDS^ pmoles of cysteine, 4 pmoles of MnC12, 0.8 pmole of CDPUNIVERSITY choline labeled with choline-1,2-C14, 5 mg. of Tween-20 4, CALIFORNIA BERKELEY H. K. SCHACHMAN (polyoxyethylene sorbitan monolaurate), and 0 25 ml. of a RECEIVED JULY 17, 1957 suspension of particles obtained from 0.25 M sucrose homogenates of chicken liver by a method already described.3 Four pmoles of substances to be tested were added as indicated. The final volume of the system was 1.0 ml., and the THE ENZYMATIC SYNTHESIS OF incubation was for 2 hours a t 37”, after which the lipides SPHINGOMYELIN1 were extracted repeatedly with hot methanol. The lipide Sir: extract was hydrolyzed in 0.4 N methanolic potassium hydroxide a t 37’ for two hours, transferred to chloroform It has been suggested2 that the enzymatic syn- and thoroughly washed.8 Aliquots of the chloroform soluthesis of sphingomyelin may take place by the tion were then plated and counted.

The term (Sp - sp) which may be very small, about 0.05 svedbergs, can be measured accurately by the differential technique. The same optical principles may be useful in the direct measurement of small changes in molecular weights and diffusion coefficients.

transfer of the phosphorylcholine moiety of cytidine diphosphate choline (CDP-choline) to the primary hydroxyl group of an N-acylsphingosine (ceramide) in a reaction fundamentally similar to the enzymatic synthesis of lecithin3 Cyt-P-P-choline

+ Ceramide Sphingomyelin

+ Cyt-P

(1)

An enzyme (phosphorylcholine-ceramide transferase) has now been found in chicken liver which catalyzes an extensive net synthesis of sphingomyelin from C14-labeled CDP-choline and an “active ceramide.” When the enzyme incubation was run on a large scale (100 ml.) under the conditions described in Table I, 25.5 mg. of enzymatically synthesized phospholipide was isolated by chromatography on silicic acid and identified as sphingomyelin by the following properties : stability toward mild alkaline hydrolysis ; insolubility in ether and acetone; N / P ratio of 2.08; and an infrared spectrum closely resembling that of purified sphingomyelin. The purity of the isolated product, based on comparison of its specific radioactivity with that of the CDP-choline used, was a t least 90%. The enzyme is highly specific, both for CDPcholine and “active ceramide.” Ceramides with short-chain fatty acids in amide linkage are much more active than long-chain fatty acid amides, presumably because the short chain compounds are more soluble and penetrate more readily t o the enzyme surface. N-Acetyldihydrosphingosineand N-acetylphytosphingosine are inactive (Table I). Acetylation of crude sphingosine (obtained by acid hydrolysis of cerebrosides) with acetic anhydride (1) Supported by grants from the Nutrition Foundation, the Life Insurance Medical Research Fund and the United States Public Health Service (B-1199). The authors are indebted to Dr. H. E. Carter for the infrared spectral analyses and for helpful discussions. (2) M. Sribney and E. P. Kennedy, Federation Proc., 16, 253 (1957). (3) E. P. Kennedy and S. B. Weiss. J . Biol. Chem., 222, 193 (1956).

I

in the presence of alkali4 leads t o the formation of “active ceramide.” In contrast, N-acetylsphingosine prepared by treatment of recrystallized triacetylsphingosine with alkali shows little activity, but it is converted to “active ceramide” by heating with acetic-sulfuric acid. It is concluded that the sphingosine portion of “active ceramide” does not possess the D-erythro-trans-sphingosine structure which has been definitely established for the triacetylsphingosine described by Carter415and the N-acetylsphingosine derived from it. This result is unexpected in view of the evidence6that naturally occurring sphingolipides are also of the D-erythrotrans structure. Two possibilities appeared most likely. The “active ceramide” might either have the cis rather than the trans configuration a t the double bond, or the threo rather than the erythro relationship of the amino group to the hydroxyl on C-3. Generous TABLE I1 ACTIVITYOF ISOMERS OF N-ACETYLSPHINGOSINE AS ExZYMATIC PRECURSORS OF SPHINGOMYELIN Additions

Experiment 1 PI’-Acetyl-DL-erpthro-trans-sphingosine6 l\’-Acetyl-DL-threo-trans-sphingosine6

Sphingomyelin synthesized millimicromoles

4 105

Experiment 2 N-Acetyl-~r.-erythro-trans-sphingosine? 5 h~-Acetyl-~~-threo-trans-sphingosine7 83 N-Acetyl-~~-erythro-cis-sphingosine7 1 N-Acetyl-~~-threo-cis-sphingosine~ 1 The conditions of the experiment were the same as shown in Table I. Four pmoles of the N-acetyl derivatives of the sphingosine isomers was added as shown. (4) H. E. Carter, W. P. Norris, F. J. Glick, G. E. Phillips and R. Harris, ibid., 170, 269 (1947). (5) H. E. Carter, D. S. Galanos and Y. Fujino, Can. J . Biochnnr. Phyriol., 34, 320 (1956).