Metabolic regulation of the squid nerve Na⁺/Ca²⁺ exchanger: recent kinetic, biochemical and structural developments

The Na?/Ca2? exchangers are structural membrane proteins, essential for the extrusion of Ca2? from most animal cells. Apart from the transport sites, they have several interacting ionic and metabolic sites located at the intracellular loop of the exchanger protein. One of these, the intracellular Ca2? regulatory sites, are essential and must be occupied by Ca2? to allow any type of ion (Na? or Ca2?) translocation. Intracellular protons and Na? are inhibitory by reducing the affinity of the regulatory sites for Ca2?; MgATP stimulates by antagonizing H? and Na?. We have proposed a kinetic scheme to explain all ionic and metabolic regulation of the squid nerve Na?/Ca2? exchanger. This model uniquely accounts for most of the new kinetic data provided here; however, none of the existing models can explain the trans effects of the Ca(i)2?-regulatory sites on external cation transport sites; i.e. all models are incomplete. MgATP up-regulation of the squid Na?/Ca2? exchanger requires a cytosolic protein, which has been recently identified as a member of the lipocalin super family of Lipid Binding Proteins (LBP or FABP) of 132 amino acids (ReP1-NCXSQ, access to GenBank EU981897). This protein was cloned, expressed and purified. To be active, ReP1-NCXSQ must be phosphorylated from MgATP by a kinase present in the plasma membrane. Phosphorylated ReP1-NCXSQ can stimulate the exchanger in the absence of ATP. Experiments with proteoliposomes proved that this up-regulation can take place just with the lipid membrane and the exchanger protein. The structure of ReP1-NCXSQ predicted from the amino acid sequence has been confirmed by X-ray crystal analysis; it has a "barrel" formed by ten beta sheets and two alpha helices, with a lipid coordinated by hydrogen bonds with Arg 126 and Tyr 128.     

Economics,human biology and inequality: A review of “puzzles” and recent contributions from a Deatonian perspective

The Nobel laureate Angus Deaton concentrated his work on puzzling developments and phenomena in economics. Puzzles are exciting elements in economics, because readers feel challenged by the question of how they can be solved. Among the puzzles analyzed by Deaton are: (1) Mortality increase of white, U.S. non-Hispanic men (2000 to today); (2) Why are height and income sometimes closely correlated, but not always?; (3) Height inequality among males and females; and (4) The Indian puzzle of declining consumption of calories during overall expenditure growth.This article reviews these “puzzles” and the main insights that Deaton derived from their discussion insofar as they pertain to the biological aspects of human development. I will focus on the field of this journal, Economics and Human Biology, in which Deaton has been very active over the last two decades. I will also document some of the responses by other scholars and their contributions to these puzzles, as they relate to the field of economics and human biology.     

The 8~(th) International Workshop on Trichoderma and Gliocladium“TRICHODERMA AND THE ENVIRONMENT”

20 - 2 3September,2 0 0 4ZhejiangUniversity ,Hangzhou ,CHINAINVITATIONOnbehalfoftheOrganizingCommitteeofthe 8thInternationalWorkshoponTrichodermaandGliocladium ,wetakegreatpleasureinextendinganinvitationtoyoutovisitHangzhouinSeptember2 0 0 4 .Wearehonoredtoorga nizeforthefirsttimethewokshopinanAsiancountry .WelookforwardtohostingasmanyofyouaspossibleforaninspiringexchangeofideasandinformationwithfocusoftheWorkshoptopic :TRICHODERMAANDTHEENVIRONMENT .Thescientificprogramw…     

“Lost sugars” — reality of their biological and medical applications

The glycan chains attached to cell surfaces or to single proteins are highly dynamic structures with various functions. The glycan chains of mammals and of some microorganisms often terminate in sialic acids or α-1,3-galactose. Although these two sugars are completely distinct, there are several similarities in their biological and medical importance. First, one type of sialic acid, N-glycolylneuraminic acid, and the galactose bound by an α-1,3-linkage to LacNAc, that forms an α-gal epitope, were both eliminated in human evolution, resulting in the production of antibodies to these sugars. Both of these evolutionary events have consequences connected with the consumption of foods of mammalian origin, causing medical complications of varying severity. In terms of ageing, sialic acids prevent the clearance of glycoproteins and circulating blood cells, whereas cryptic α-gal epitopes on senescent red blood cells contribute to their removal from circulation. The efficiency of therapeutic proteins can be increased by sialylation. Another common feature is the connection with microorganisms since sialic acids and α-gal epitopes serve as receptors on host cells and can also be expressed on the surfaces of some microorganisms. Whereas, the sialylation of IgG antibodies may help to treat inflammation, the expression of the α-gal epitope on microbial antigens increases the immunogenicity of the corresponding vaccines. Finally, sialic acids and the α-gal epitope have applications in cancer immunotherapy. N-glycolylneuraminic acid is a powerful target for cancer immunotherapy, and the α-gal epitope increases the efficiency of cancer vaccines. The final section of this article contains a brief overview of the methods for oligosaccharide chain synthesis and the characteristics of sialyltransferases and α-1,3-galactosyltransferase.     

Symposium on Biochemistry and Molecular Biology of Plant Fatty Acids and Glycerolipids (Fallen Leaf Lake,California, United States,June 4–8, 2003)

Russian Journal of Plant Physiology -