Membrane proteins processes

All the long-range forces discussed in this chapter play a role in biological processes. Interactions between membranes, proteins, ligands, antibodies... 

The discrepancy arises because ATP is used to drive processes which are not directly related to growth, eg membrane transport processes, protein turnover. These are called the maintenance and dissipation demands for ATP. 

Ultrafiltration (UF) is used for the separation and concentration of macromolecules and colloidal particles. Ultrafiltration membranes usually have larger pore sizes than RO membranes, typically 1 to 100 nanometer (nm). Operating pressures are generally low (30-100 psig). Applications include electropaints, gray water, emulsions, oily wastes, and milk, cheese, and protein processing. 

While the fluid mosaic model of membrane stmcture has stood up well to detailed scrutiny, additional features of membrane structure and function are constantly emerging. Two structures of particular current interest, located in surface membranes, are tipid rafts and caveolae. The former are dynamic areas of the exo-plasmic leaflet of the lipid bilayer enriched in cholesterol and sphingolipids they are involved in signal transduction and possibly other processes. Caveolae may derive from lipid rafts. Many if not all of them contain the protein caveolin-1, which may be involved in their formation from rafts. Caveolae are observable by electron microscopy as flask-shaped indentations of the cell membrane. Proteins detected in caveolae include various components of the signal-transduction system (eg, the insutin receptor and some G proteins), the folate receptor, and endothetial nitric oxide synthase (eNOS). Caveolae and lipid rafts are active areas of research, and ideas concerning them and their possible roles in various diseases are rapidly evolving. 

As described earlier, the inside-outside asymmetry of membrane proteins is stable, and mobifity of proteins across (rather than in) the membrane is rare therefore, transverse mobility of specific carrier proteins is not likely to account for facilitated diffusion processes except in a few unusual cases. 

Secretory proteins and proteins destined for membranes distal to the ER completely traverse the membrane bilayer and are discharged into the lumen of the ER. 7V-Glycan chains, if present, are added (Chapter 47) as these proteins traverse the irmer part of the ER membrane—a process called cotranslational glycosyla-tion. Subsequently, the proteins are found in the... 

The biogenesis of membranes is thus a complex process about which much remains to be learned. One indication of the complexity involved is to consider the number of posttranslational modifications that membrane proteins may be subjected to prior to attaining their mamre state. These include proteolysis, assembly... 

Up to now, the pectinolytic enzymes of E. chrysanthemi that have been detected were extracellular secreted enzymes (PelA, B, C, D, E, L, exo-Peh and PemA), periplasmic (exo-Pel), or cytoplasmic (OGL) proteins (1, 5). In contrast, PemB is an outer membrane pectinolytic enzyme. To our knowledge it is the first pectinase characterised as a membrane protein. We presented several lines of evidence showing that PemB is a lipoprotein (i) Its N-terminal sequence has the characteristics of lipoprotein signal sequences, (ii) PemB is synthesised as a high molecular weight precursor processed into a lower molecular weight mature form, (iii) Palmitate, the most prevalent fatty acid in bacterial lipoproteins (12), is incorporated into PemB. 

In this chapter, a novel interpretation of the membrane transport process elucidated based on a voltammetric concept and method is presented, and the important role of charge transfer reactions at aqueous-membrane interfaces in the membrane transport is emphasized [10,17,18]. Then, three respiration mimetic charge (ion or electron) transfer reactions observed by the present authors at the interface between an aqueous solution and an organic solution in the absence of any enzymes or proteins are introduced, and selective ion transfer reactions coupled with the electron transfer reactions are discussed [19-23]. The reaction processes of the charge transfer reactions and the energetic relations... 

The reduction of O2 is usually believed to proceed accompanying the transfer of protons or other ions through a biomembrane [5], and the reaction rate or even the process is considered to vary depending on the kind of transferring ions. An ion channel or ion pump composed of membrane proteins has often been assumed in the explanation of the dependency of the reaction rate [5]. 

The mechanisms of the oscillations in biomembranes have been explained based on the gating of membrane protein called an ion channel, and enormous efforts have been made to elucidate the gating process, mainly by reconstitution of channel proteins into bilayer membranes [9-11]. 

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