Membrane fractions

Fig. 4. FSH receptor-binding potencies of equine FSH ( ), eCG purified from pregnant mate s semm (O), and endometrial cups (A). Receptor-binding in ceU membrane fractions, B/Bq from (a) horse, (b) calf, and (c) rodent testes (40). Courtesy of Butterworth-Heinemaim.

Nonselective membranes can assist enantioselective processes, providing essential nonchiral separation characteristics and thus making a chiral separation based on enantioselectivity outside the membrane technically and economically feasible. For this purpose several configurations can be applied (i) liquid-liquid extraction based on hollow-fiber membrane fractionation (ii) liquid- membrane fractionation and (iii) micellar-enhanced ultrafiltration (MEUF). 

In the short term, we do not expect chiral membranes to find large-scale application. Therefore, membrane-assisted enantioselective processes are more likely to be applied. The two processes described in more detail (liquid-membrane fractionation and micellar-enhanced ultrafiltration) rely on established membrane processes and make use of chiral interactions outside the membrane. The major advantages of these... 

Squalene epoxidase, like most enzymes responsible for the later steps of sterol biosynthesis [43, 51], is membrane-bound which makes its purification in native form challenging. The purification is additionally complicated by the presence of a large number of cytochrome P450 and other enzymes that have similar hydro-phobicity and size as squalene epoxidase and are hence difficult to remove [52]. Most studies have been carried out with rat liver microsome squalene epoxidase either partially purified or as a homogenate of the cell membrane fraction. In vitro reconstitution of squalene epoxidase activity is absolutely dependent on molecular oxygen, NADPH, FAD, and NADPH-cytochrome c reductase [52, 53]. In this respect, squalene epoxidase resembles the cytochrome P450 enzymes described... 

Alzheimer s disease Amount of m-calpain in the cytosolic but not the membranous fractions and in the neurofibrillary tangles of brain from Alzheimer s patients is increased37,38... 

PPCs Prenylation is the post-translational addition of 15- or 20-carbon isoprenyl lipids to the C-terminus of proteins. Prenylation is an irreverable modification that anchors proteins to the membrane fraction of cells. 

Many different glycosyltransferase activities involved in higher plant wall biosynthesis have been identified in cell free membrane fractions, but in only a few cases has glycosyltransferase activity been retained in detergent-solubilized preparations, and in even fewer cases have any purified polypeptides been identified as plant cell wall glycosyltransferases (29,33). 

A. Western blot analysis of membrane fractions from P. vulgaris probed with a PGIP-specific antibody. 1) PGIP purified from P. vulgaris] 2) and 3) membranes 4) supernatant of the membrane preparation. 

The PemB cellular localisation was determined both in E. chrysanthenu and in an E. coli recombinant strain by Western blot of the cell fractions with a PemB-antiserum. No PemB was detected in the culture supernatant and only trace amounts were found in the soluble cell fractions - periplasm and cytoplasm (Figure 2). PemB was found mostly in the total membrane fraction from which it could be completely extracted by Triton X-100/Mg2+ and partially extracted by Sarkosyl (Figure 2). This behaviour is typical of inner membrane proteins, but since some exceptions have been noticed it does not positively indicate the PemB localisation (15). We performed cell membrane fractionation in sucrose density gradient centrifugation both by sedimentation and flotation, using several markers of inner and outer membrane vesicles. PemB was found in the outer membrane vesicles (data not shown). 

Figure 2. PemB cellular localisation. (A) Fractionation of E. chrysanthemi cells by spheroplasting. Lane 1, culture supernatant lane 2, total cell lysate lane 3, periplasmic fraction lane 4, crude membrane fraction lane 5, cytoplasmic fraction. (B) Detergent extraction of PemB from E. chrysanthemi A837 cell envelopes. Lane 1 crude envelope fraction lane 2 Triton-soluble fraction lane 3 Triton-insoluble fraction lane 4 Sarkosyl-soluble fraction lane 5 Sarkosyl-insoluble fraction.

Figure 4. Purification of PemB from E. coli K38 pGPl-2/pPME6-5 cells. Proteins were separated by urea-SDS-PAGE. Lane 1, induced cell lysate lane 2, soluble protein fraction from induced cells lane 3, membrane fraction from non-induced cells lane 4, membrane fraction from induced cells lane 5, membrane proteins not extracted by Triton X-100 lane 6, membrane proteins extracted by Triton X-100 lane 7, PemB purified by preparative electrophoresis. The molecular weight standard positions are indicated.

Saffarini DA, SL Blumerman, KJ Mansoorabadi (2002) Role of menaquinones in Fe(III) reduction by membrane fractions of Shewanella putrefaciens. J Bacteriol 184 846-848. 

Le Page, KN., Cheeseman, K.H., Osman, N. and Slater, T.F. (1988). Lipid peroxidation in purified plasma membrane fractions of rat liver in relation to the toxicity of carbon tetrachloride. Cell Biochem. Function 6, 87-99. 

Most receptors (a notable exception being the steroid receptors that influence DNA transcription) are located on the cell surface, and purified cell membranes are thus an obvious choice of preparation. When a tissue is homogenized, however, any membrane fraction isolated may well contain membranes from intracellular organelles in addition to cell membranes from all the cell types present in the tissue. Thus, brain membranes will contain membranes not only from neurons but... 

NPQ (Rakhimberdieva et al. 2004) exactly matches the absorption spectrum of the carotenoid, 3 -hydrox yech i nenone (Polivka et al. 2005) in the OCP. The OCP is now known to be specifically involved in the phycobilisome-associated NPQ and not in other mechanisms affecting the levels of fluorescence such as state transitions or D1 damage (Wilson et al. 2006). Studies by immunogold labeling and electron microscopy showed that most of the OCP is present in the interthylakoid cytoplasmic region, on the phycobilisome side of the membrane, Figure 1.2 (Wilson et al. 2006). The existence of an interaction between the OCP and the phycobilisomes and thylakoids was supported by the co-isolation of the OCP with the phycobilisome-associated membrane fraction (Wilson et al. 2006, 2007). 

Smith, W.D., Smith, S.K and Murray, J.M. (1994) Protection studies with integral membrane fractions of Haemonchus contortus. Parasite Immunology 16, 231—241. 

Translation-competent ER membrane fractions can also be prepared from tissue culture cells. We recommend a terminally differentiated secretory suspension cell line, such as a plasmacytoma (e.g., J558L), which contains abundant levels of ER membrane. In this protocol, cells are collected by centrifugation (5 min, 500 x g) and resuspended in a homogenization buffer containing 10 mMKOAc, 10 mMK-HEPES, pH 7.5, 1.5 mMMg(OAc)2,... 

In a typical experiment, paired reactions will be performed where either mRNA or RM are absent, to confirm that all translation products derive from the intended mRNA and reflect the activity of ER-bound ribosomes. As an additional control, mock translations can be performed and the membrane fraction removed by centrifugation (10 min, 60K, TLA100.2 rotor). The supernatant is then recovered, programmed with mRNA, and... 

The y and 8 forms of PLC can be distinguished from PLC(3 by the virtual absence of a 400-500 amino acid consensus sequence present in the C-terminal region of PLC(3. Consistent with the absence of putative transmembrane spanning domains, most PLC activity is localized to the cytoplasm, although a significant amount of activity is associated with membrane fractions. 

The association of PDE isozymes with the cell membrane is mediated by a conserved, hydrophobic sequence in the amino terminus of the proteins. This has been most convincingly demonstrated for PDE4A when the amino terminus is removed PDE4A is no longer localized to the membrane fraction. A similar amino terminus sequence is found in the membrane-bound forms of PDE2, and may also mediate the membrane-association of certain PDE3 isozymes. 

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