Electrophoretic characterization of proteins in the plasma membrane of porcine spermatozoa

Similar documents
Supplementary material: Materials and suppliers

potassium is included in the dialysis fluid. Unless the phosphate buffer

SCS MOLECULAR WEIGHT MARKERS 2,500-17,000 Caltons

DEPENDENCE OF SPERM MOTILITY AND RESPIRATION ON OXYGEN CONCENTRATION

note on methodology I

Antigenic Analysis of Isolated Polypeptides from Visna Virus

Protein MultiColor Stable, Low Range

MW.SDS.70L and MW-SDS.200 Kits

Mammalian Melanosomal Proteins: Characterization by Polyacrylamide Gel Electrophoresis

Sperm populations in the female genital tract

Digestion of the zinc in human milk, cow s milk and a commercial babyfood : some implications for human infant nutrition

Ribosomal Proteins of Escherichia coli*

DIFFERENTIATION OF RABBIT SPERM ANTIGENS FROM THOSE OF SEMINAL PLASMA. (Received 18th October 1968, revised 4th April 1969)

Reconstitution of Neutral Amino Acid Transport From Partially Purified Membrane Components From Ehrlich Ascites Tumor Cells

EXPERIMENT 13: Isolation and Characterization of Erythrocyte

Trypsin Mass Spectrometry Grade

Staphylococcus aureus

Epididymal proteins mimic the androgenic effect on

(Received 8th October 1973)

Lipid phase transition in the plasma membrane of the goat epididymal maturing spermatozoa

IMMUNOLOGIC REACTIVITY IN HUMAN BREAST CANCER AGAINST CULTURED HUMAN BREAST TUMOR CELLS

Summary. Mouse eggs were fertilized in vitro, in the presence and

A Comparative Study of Distribution of Protein and Cholesterol in Various Fractions of Human Semen from Infertile and Fertile Subjects

(FITC) or rhodamine blue isothiocyanate (RBITC) for use in mixed egg-transfer experiments. Both FITC and RBITC bind to the zona pellucida

DELFIA Tb-N1 DTA Chelate & Terbium Standard

The Time of Cortical Granule Breakdown and Sperm Penetration in Mouse and Hamster Eggs Inseminated in vitro

SUPPLEMENTARY MATERIAL

(Adams 8c Purves 1958), or LATS-protector (LATS-P) (Adams 8c Kennedy. 1967). The failure of the McKenzie (1958) mouse bioassay to detect LATS in

Proteins. Amino acids, structure and function. The Nobel Prize in Chemistry 2012 Robert J. Lefkowitz Brian K. Kobilka

Motility and eosin uptake of formaldehyde-treated ram

The Use of Zona-Free Animal Ova as a Test-System for the

EFFECT OF DRYING ON PROTEIN PROFILE OF MURRAYA KOENIGII LEAVES S. Satheshkumar 1* and N. Punniamurthy 2

STUDIES ON ASPIRIN ESTERASE OF HUMAN SERUM. Masako MORIKAWA, Michiko INOUE, Minoru TSUBOI. and Mamoru SUGIURA*

HiPer Western Blotting Teaching Kit

Sequential Extraction of Plant Metabolites

Work-flow: protein sample preparation Precipitation methods Removal of interfering substances Specific examples:

DELFIA Eu-DTPA ITC Chelate & Europium Standard

Capacitated sperm cells react with different types of antisperm antibodies than fresh ejaculated sperm*

Annexure III SOLUTIONS AND REAGENTS

Isolation of Cytochrome C from Beef Heart BCHM 3100K-02

protein composition of plasma membranes from embryonic chick erythroid cells at various stages of maturation. Significant

DELFIA Tb-DTPA ITC Chelate & Terbium Standard

TRANSPORT OF AMINO ACIDS IN INTACT 3T3 AND SV3T3 CELLS. Binding Activity for Leucine in Membrane Preparations of Ehrlich Ascites Tumor Cells

FOCUS SubCell. For the Enrichment of Subcellular Fractions. (Cat. # ) think proteins! think G-Biosciences

Envelopes of Chlamydia psittaci in Alkaline Buffer and

IN VITRO FERTILIZATION OF RABBIT EGGS IN OVIDUCT SECRETIONS FROM DIFFERENT DAYS BEFORE AND AFTER OVULATION*

BIL 256 Cell and Molecular Biology Lab Spring, Tissue-Specific Isoenzymes

Scanning Electron Microscopic Observations on the Sperm Penetration through the Zona Pellucida of Mouse Oocytes Fertilized in vitro

Chapter 2 Transport Systems

Pinpoint Slide RNA Isolation System II Catalog No. R1007

Isolation, Purification, and Characterization of Horseradish Peroxidase (HRP) J. Kane, T. Schweickart

Purification and Some Properties of Milk-clotting Enzyme from Aspergillus niger

Chapter PURIFICATION OF ALKALINE PROTEASES

Proteases in germinating finger millet (Eleusine coracana) seeds

130327SCH4U_biochem April 09, 2013

Instructions for Use. APO-AB Annexin V-Biotin Apoptosis Detection Kit 100 tests

The total protein test is a rough measure of all of the proteins in the plasma. Total protein measurements can reflect:

Partial purification of Rho(D) antigen from Rh positive and negative erythrocytes (Rh antigen/affinity chromatography/lw antigen)

Interaction of lanthanum chloride with human erythrocyte membrane in relation to acetylcholinesterase activity

MORPHOLOGIC CHARACTERISTICS OF THE CHEMICALLY INDUCED ACROSOME REACTION IN HUMAN SPERMATOZOA*

Chiang Mai, 50200, Thailand

Development: is the growth of an individual organism from a simple to a more complex or mature level. A slow process of progressive change

PARTIAL PURIFICATION AND IMMUNO-BIOCHEMICAL CHARACTERISATION OF FERTILITY ASSOCIATED PROTEIN OF KARAN FRIES BULL SEMINAL PLASMA

Approximately 8 min were required for the cortical granule material

The effect of phosphatidyl choline on the degradation of phosphatidyl ethanolamine by the phospholipase of post-heparin plasma or snake venom

Procaspase-3. Cleaved caspase-3. actin. Cytochrome C (10 M) Z-VAD-fmk. Procaspase-3. Cleaved caspase-3. actin. Z-VAD-fmk

Surface of the Equatorial Segment of the

CHEMICAL STUDIES ON BACTERIAL AGGLUTINATION II. THE IDENTITY OF PRECIPITIN AND AGGLUTININ* BY MICHAEL HEIDELBERGER, PH.D., AND ELVIN A.

Characterization of Anti-Hamster ZP-0 Monoclonal Antibody

Differential acetylcholinesterase activity in rat cerebrum, cerebellum and hypothalamus

ab Cell Invasion Assay (Basement Membrane), 24-well, 8 µm

Materials and Methods. Spermatozoa. Experiment 2. Experiment 3. Experiment 1

Paper 2 Data Analysis and Planning For Examination from 2016 SPECIMEN PAPER 1 hour 15 minutes

N-Glycosidase F Deglycosylation Kit

however, and the present communication is concerned with some of

PRODUCT: RNAzol BD for Blood May 2014 Catalog No: RB 192 Storage: Store at room temperature

ab Glycated Protein Detection Kit

EFFECT OF THAWING RATE AND POST-THAW TEMPERATURE ON MOTILITY AND ACROSOMAL MAINTENANCE IN BOVINE SEMEN FROZEN IN PLASTIC STRAWS l,2

The University of ~ukurova, Art & Science Faculty, Department of Chemistry, BaIcali, Adana-TURKEY

antigen Y. Kajita, D. Morgan, A.B. Parkes and B. Rees Smith

ON THE DIFFERENCE IN ADSORPTION ON SEPHADEX GEL OF THE DEXTRANSUCRASE OF STREPTOCOCCUS BOVIS GROWN ON SUCROSE AND GLUCOSE MEDIA

than normal (1), whereas RNA and protein synthesis in megaloblastic erythroblasts is unaffected (2). The

Activation of proacrosin accompanies upregulation of sp32 protein tyrosine phosphorylation in pig sperm

SUPPLEMENTARY INFORMATION. Bacterial strains and growth conditions. Streptococcus pneumoniae strain R36A was

TECHNICAL BULLETIN. R 2 GlcNAcβ1 4GlcNAcβ1 Asn

Collagenase Assay Kit

TRACP & ALP Assay Kit

Keratin-like Proteins in Corneal and Conjunctival Epithelium are Different

CoQ10(Coenzyme Q10) ELISA Kit

I mutants accumulate pyruvate when growing in the presence of isoleucine and

Cell Lysis Buffer. Catalog number: AR0103

In-vitro fertilization ofhamster eggs in different media and

glucose as substrate for bull spermatozoa has been measured: fructose Spermatozoa of the higher mammalians (e.g. bull, dog and human) are known

Pelagia Research Library

ISOLATION AND PROTEIN PATTERN OF EYE LENS FIBER JUNCTIONS

Protocol for Gene Transfection & Western Blotting

studied were the lymphoblasts from 3 cases of acute lymphatic leukaemia (ALL) and the lymphocytes from 5 such patients in complete remission.

Step 4. Step 4. Choose MW markers. Choose MW markers. Gel Electrophoresis of Proteins

Transcription:

Electrophoretic characterization of proteins in the plasma membrane of porcine spermatozoa K. L. Esbenshade and E. D. Clegg Department ofanimal Sciences, Purdue University, West Lafayette, Indiana 47907, U.S.A. Using immunological and cytochemical methods, several investigators have demonstrated that components on the surface of spermatozoa are altered during exposure of the spermatozoa to the female reproductive tract (Johnson & Hunter, 1972; Aonuma et al., 1973; Oliphant & Brackett, 1973). Recent evidence indicates that capacitation may also involve subtle modifications in the chemical composition of sperm membranes (Snider & Clegg, 1975). The plasma membrane of porcine spermatozoa is being characterized in our laboratory to provide a foundation for subsequent studies of chemical changes during capacitation. In this paper, electrophoretic separation and partial characterization of proteins from plasma membrane of porcine spermatozoa is reported. Plasma membrane was isolated from porcine spermatozoa by the procedure of Lunstra, Clegg & Morr\l=e'\(1974). Briefly, sperm-rich semen was filtered at the time of collection through Miracloth (Chicopee Mills, Inc., New York, N.Y.) and then filtered through glass wool moistened with Ca-free Ringer solution. After low-speed centrifugation, spermatozoa were resuspended in Ringer-EDTA. The sperm suspension was cooled and sonicated under conditions that removed plasma membrane from the acrosomal region of the sperm head, but minimized disruption of other sperm membranes. After centrifugation at 6000 g for 10 min the plasma membrane-rich supernatant was bottomloaded in a discontinuous sucrose gradient (sucrose solutions with dzo 114, 117 and 1-22) and centrifuged at 100,000g for 90 min. Plasma membrane was recovered from the d= 114/117 inter face, diluted with 1 mm-sodium bicarbonate and centrifuged to sediment the membrane vesicles. The purity of plasma membrane isolated by this procedure has been assessed by quantitative morphometry (Lembi, Morré, St-Thomson & Hertel, 1971). After embedding for electron micro scopy, thin sections were de-stained with periodic acid and then stained with acidic phosphotungstic acid (Morré, Clegg, Lunstra & Mollenhauer, 1974). Under those conditions, the plasma membrane was the only membrane of porcine spermatozoa that was stained. Our preparations routinely contained 75-80% plasma membrane, with outer acrosomal membrane being the major contamin ant. Other studies in this laboratory (unpublished data) show that the electrophoretic pattern of the proteins from purified outer acrosomal membrane is quite different from that of proteins from purified plasma membrane, indicating that the amount of outer acrosomal membrane in the prepara tions did not substantially alter the separation pattern. Since some acrosomes were ruptured by the mild sonication of spermatozoa during plasma membrane isolation, it was possible that proteolytic activity could act on proteins of the plasma membrane. If that occurred, proteins extracted from the plasma membrane would include peptides that could appear as additional bands in electrophoresis. To minimize proteolytic activity, samples were cooled to 0 to 5 C before sonication and maintained at that temperature. Also, the ph of the preparation was kept at approximately 5-5. The specific activity of porcine acrosin, which is maximal at ph 8-5 (Polakoski, McRorie & Williams, 1973), slow at ph 5-5. When photographic emulsion plates were used to detect proteolytic activity (Penn, Gledhill & Darzynkiewicz, 1972) during the isolation procedure, no dispersion of the silver granules was observed. Protein determinations were performed by the method of Lowry, Rosebrough, Farr & Randall (1951). Two systems of polyacrylamide gel electrophoresis (PAGE) were used to separate plasma membrane proteins. To obtain estimates of the molecular weights of protein bands, proteins were solubilized with sodium dodecyl sulphate (SDS) and urea at neutral ph and separated on SDS- PAGE gels (8% acrylamide) as described by Zahler (1975). Purified protein standards of known 333

- 334. L. Esbenshade and E. D. Clegg molecular weight were subjected to electrophoresis under identical conditions and a quadratic equation was calculated by the least squares method to express molecular weight as a function of relative mobility in the gel. Relative mobility is the migration of a protein in the gel expressed as a fraction of the distance travelled by the tracking dye bromophenol blue (Weber & Osborn, 1969). The standard proteins used in these experiments were fibrinogen, -globulin, bovine serum albumin, ovalbumin, ct-chymotrypsinogen, myoglobin and cytochrome c (Sigma Chemical Co., St Louis MO). Molecular weights of plasma membrane protein bands were estimated from their respective relative mobilities. In addition to SDS-PAGE, plasma membrane proteins were separated on 7-5 % acrylamide gels in an acidic system using phenol, urea and acetic acid to solubilize the membrane proteins (Zahler, 1975). Proteins in the SDS-PAGE gels were stained by a procedure that simultaneously removed the SDS from the gels. The gels were placed in test tubes and treated at room temperature as follows : washed in 25% isopropyl alcohol and 10% trichloroacetic acid in water overnight; stained with 0-25% Coomassie Blue in 25% aqueous isopropyl alcohol containing 10% acetic acid for 6 hr; de-stained by washing in 10% isopropyl alcohol and 10% acetic acid in water for 1 hr; and de-stained electrophoretically for 1 hr with methanol : acetic acid: water (2:3:35, by vol.). Glycoproteins were stained with periodic acid-schiff (PAS) reagent by the procedure of Fairbanks, Steck & Wallach (1971). Proteins in gels from the acidic system were stained with 0-25 % Coomassie Blue in 7 % acetic acid and de-stained with 7 % acetic acid. The standard curve calculated from SDS-PAGE to express the relationship between molecular weight and relative mobility was : Y 1-851X2 3092X 4-5-447 = where Y represents the logi0 of molecular weight and X represents relative mobility. The coefficient of correlation for that equation was 0-9992. Although a straight line is used normally to express the relationship between the logarithm of the molecular weight and relative mobility (Weber & Osborn, 1969), more information could be obtained in this study if the relationship was expressed as a quad ratic curve. With 8 % acrylamide gels, most proteins with molecular weights up to about 200,000 follow a straight-line relationship. Proteins with molecular weights between 200,000 and 300,000 can enter the gels and migrate shorter distances, but the linear relationship between the logarithm of the molecular weight and relative mobility does not remain valid. With a quadratic curve, the molecular weight range could be extended to include proteins with molecular weights between 200,000 and 300,000. Table 1. Relative mobilities and molecular weights of the prominent proteins in plasma membrane of porcine spermatozoa separated by sodium dodecyl sulphatepolyacrylamide gel electrophoresis Proteins as migrated from origin Relative mobilities* Molecular weight 1 0-010 ± 0-001 260,000t 2 0-026 + 0-001 230,000t 3 0056 ± 0002 190,000t 4 0-088 + 0-004 155,000 5 0-090 + 0-007 150,000 6 0-104 ± 0-005 140,000t 7 0-153+0-006 100,000 8 0-236 + 0-011 66,000 9 0-327 + 0-012 43,000 10 0-507 ±0-021 22,500t 11 0-760 ± 0-014 14,500t * Values represent means for 5 replicates + S.E.M. t Carbohydrate-positive.

Proteins in pig sperm plasma membrane 335 1. Polyacrylamide gel electrophoresis (PAGE) of plasma membrane proteins from porcine spermatozoa. A, plasma membrane proteins solubilized with SDS-urea, separated by SDS-PAGE and stained with Coomassie Blue; B, same as (A) except stained with periodic acid-schiff reagent; C, plasma membrane proteins solubilized with phenol-urea-acetic acid, separated with acidic PAGE and stained with Coomassie Blue. Text-fig. With SDS-PAGE of plasma membrane proteins from porcine spermatozoa, 11 prominent bands were detected with estimated molecular weights ranging from 14,500 to 260,000 (Table 1; Text-fig. 1). In subsequent trials, improved resolution was achieved by reducing the amount of protein applied to the gels, and the bands with mean estimated molecular weights of 66,000 and 100,000 separated into two and three bands, respectively. Of the 11 bands detected originally, at least 6 contained glycoprotein. Four of the six glycoprotein bands had relatively high molecular weights (140,000 to 260,000), while the other 2 were low in molecular weight (14,500 and 22,500). A substantial amount of PAS-positive protein remained at the origin of gels in SDS-PAGE. With 8% acrylamide gels, some high molecular weight proteins should not be able to enter the polyacrylamide matrix. Therefore, the plasma membrane of porcine spermatozoa probably contains proteins, including glycoproteins, having molecular weights above 260,000. Other work in this laboratory (unpublished), using gel filtration on Sephadex G-200, supports that concept.

336. L. Esbenshade and E. D. Clegg When electrophoresis was conducted under acidic conditions so that the proteins from the plasma membrane migrated toward the cathode, 13 protein bands could be distinguished (Text-fig. 1). No attempt was made to relate individual bands in acidic PAGE to those observed in SDS- PAGE. Both methods of PAGE tended to separate the membrane proteins according to molecular weight. In the acidic gels, however, there was a tendency for migration rates to depend on sample volume. Also, not all of the protein entered the gels. That effect was probably due to exclusion of high molecular weight proteins by the 7-5% acrylamide polymer (in a manner similar to SDS-PAGE). It is also possible that some of the protein aggregated at the origin in the acidic system because of the absence of phenol in the gels. The SDS-PAGE gels were therefore more suitable for molecular weight determinations (Zahler, 1975), although separation of the membrane proteins was more distinct with the acidic system. The improved resolution with the acidic system may be due to more effective dissociation of lipids from proteins by phenol (Steck & Fox, 1972). The presence of relatively large amounts of carbohydrate in glycoproteins can reduce the staining of the protein with Coomassie Blue (Glossmann & Neville, 1971). It is therefore possible for a glyco protein band in an electrophoresis gel to be PAS-positive, but fail to stain or stain very lightly with Coomassie Blue. Under these conditions, use of densitometry with Coomassie Blue for quantification of proteins in gels would be unreliable. In addition to an effect on staining properties, the carbohydrate moiety of glycoproteins can alter the relationship between molecular weight and relative mobility by masking binding sites for SDS on the protein molecules (Segrest, Jackson, Andrews & Marchesi, 1971). The result is usually a slower migration rate of the glycoprotein during SDS-PAGE, causing the molecular weights calculated for such a protein to be too high. Therefore, the molecular weight estimations for the glycoproteins in sperm plasma membrane are probably larger than the actual values. It is likely that the protein profiles observed in these experiments represent only those proteins that are intrinsic components of the plasma membrane or are bound tightly to its surface. During the procedure for isolation of the membrane, spermatozoa were exposed to a relatively high concen tration of EDTA and to a ph of approximately 5-5. Those conditions, which were necessary to prevent agglutination, could remove loosely-bound proteins from the surface of the spermatozoon. Further experiments must be conducted to determine the extent of such loss from the plasma mem brane and the nature of the proteins removed. In the plasma membrane of spermatozoa, the carbohydrate moieties of the high molecular weight glycoproteins are probably located on the exterior surface of the cell. This hypothesis is supported by research which demonstrated that plant lectins bound to the plasma membrane of spermatozoa (Nicolson, Lacorbiere & Yanagimachi, 1972 ; Nicolson & Yanagimachi, 1972 ; Gordon, Dandekar & Bartoszewicz, 1974) and provides an explanation for the net negative charge of sperma tozoa (Cooper & Bedford, 1971). In addition, alteration of the carbohydrate groups of the surface glycoproteins may be important in capacitation. Gordon et al (1974) demonstrated that binding of concanavalin A was reduced after capacitation, and Vaidya, Glass, Dandekar & Johnson (1971) have shown that the electrophoretic mobility of spermatozoa incubated in the uterus of oestrous females was significantly less than that of intact, ejaculated spermatozoa. This investigation was supported by NIH Research Grant HD 07013. The cooperation of Mr F. H. Azzazi in providing access to unpublished results is appreciated. Journal Paper No. 6077 of the Purdue University Agricultural Experiment Station. References AoNUMA, S., Mayumi, T., Suzuki, L., Noguchi, T., IwAi, M. & Okabe, M. (1973) Studies on sperm capacitation. I. The relationship between a guineapig sperm-coating antigen and a sperm capacitation phenomenon. /. Reprod. Fert. 35, 425-432. Cooper, G.W. & Bedford, J.M. (1971) Acquisition of surface charge by the plasma membrane of mammalian spermatozoa during epididymal maturation. Anat. Ree. 169, 300-301, Abstr. Fairbanks, G., Steck, T.L. & Wallach, D.F.H. (1971) Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane. Biochemistry, N. Y. 10, 2606-2617. Glossmann, H. & Neville, D.M., Jr (1971) Glyco-

Proteins in pig sperm plasma membrane 337 proteins of cell surfaces. Comparative study of three different cell surfaces of the rat. J. biol. Chem. 246, 6339-6346. Gordon, M., Dandekar, P.V. & Bartoszewicz, W. (1974) Ultrastructural localization of surface receptors for concanavalin A on rabbit spermatozoa. /. Reprod. Fert. 36, 211-214. Johnson, W.L. & Hunter, A.G. (1972) Seminal antigens: their alteration in the genital tract of female rabbits and during partial in vitro capacitation with beta amylase and beta glucuronidase. Bio!. Reprod. 7, 332-340. Lembi, CA., Morré, D.J., St-Thomson,. & Hertel, R. (1971) N-1-Napthylphthalamic-acid-binding act ivity of a plasma membrane-rich fraction from maize coleoptiles. Planta 99, 37^15. Lowry, O.H., Rosebrough, N.J., Farr, A.L. & Randall, R.J. (1951) Protein measurement with the Folin phenol reagent. /. biol. Chem. 193, 265-275. Lunstra, D.D., Clegg, E.D. & Morré, D.J. (1974) Isolation of plasma membrane from porcine sperma tozoa. Prep. Biochem. 4, 341-352. Morré, D.J., Clegg, E.D., Lunstra, D.D. & Mollenhauf.r, H.H. (1974) An electron-dense stain for isolated fragments of plasma and acrosome mem branes from porcine sperm. Proc. Soc. exp. Biol. Med. 145, 1-6. Nicolson, G.L. & Yanagimachi, R. (1972) Terminal saccharides on sperm plasma membranes: identi fication by specific agglutinins. Science, N. Y. 177, 276-279. Nicolson, G.L., Lacorbiere, M. & Yanagimachi, R. (1972) Quantitative determination of plant agglu tinin membrane sites on mammalian spermatozoa. Proc. Soc. exp. Biol. Med. 141, 661-663. Oliphant, G. & Bracket!, B.G. (1973) Immunological assessment of surface changes of rabbit sperm undergoing capacitation. Biol. Reprod. 9, 404-414. Penn,., Gledhill, B.L. & Darzynkiewicz, Z. (1972) Modification of the gelatin substrate pro cedure for demonstration of acrosomal proteolytic activity. /. Histochem. Cytochem. 20, 499-506. Polakoski, K.L., McRorie, R.A. & Williams, W.L. (1973) Boar acrosin. I. Purification and preliminary characterization of a proteinase from boar sperm acrosomes. /. biol. Chem. 248, 8178-8182. Segrest, J.P., Jackson, R.L., Andrews, E.P. & Marchesi, V.T. (1971) Human erythrocyte mem brane glycoprotein: a re-evaluation of the molecular weight as determined by SDS polyacrylamide gel electrophoresis. Biochem. Biophys. Res. Commun. 44, 390-395. Snider, D.R. & Clegg, E.D. (1975) Alteration of phospholipids in porcine spermatozoa during in vivo uterus and oviduct incubation. J. Anim. Sci. 40, 269-274. Steck, T.L. & Fox, CF. (1972) Membrane proteins. In Membrane Molecular Biology, pp. 27-75. Eds C. F. Fox & A. D. Keith. Sinavar Associates, Stanford, Connecticut. Vaidya, R.., Glass, R. H., Dandekar, P. & Johnson, K. (1971) Decrease in the electrophoretic mobility of rabbit spermatozoa following intra-uterine incu bation. /. Reprod. Fert. 24, 299-301. Weber, K. & Osborn, M. (1969) The reliability of mo lecular weight determinations by dodecyl sulfatepolyacrylamide gel electrophoresis. /. biol. Chem. 244, 4406-4412. Zahler, W.L. (1975) Analytical polyacrylamide gel electrophoresis and molecular weight determination. Meth. Enzymol. 32, 70-81. Received 1 November 1975