A facile and green preparation of durian shell-derived carbon electrodes for electrochemical double-layer capacitors

A facile and green preparation of high surface area activated carbons with mixed microporosity and mesoporosity from durian shell waste is reported in this work. The pore structure and surface chemistry of the parent carbon were modified by the combination of ultrasonication and microwave irradiation techniques. The effects of temperature and time in the ultrasonication treatment and power output and time in the microwave irradiation were studied. The electrochemical performance of carbon electrodes for supercapacitors was tested by cyclic voltammeter (CV) and galvanostatic charge–discharge. The results show that the capacitive energy storage of electrodes is critically dependent on the microporosity and surface chemistry of activated carbons. The highest electrode capacitance in this work was 103.6 F/g that prepared from activated carbon modified at an ultrasonication temperature of 323.15 K for 10 min and microwave power output of 900 W for 10 min.     

Crystal structure of an HIV-binding recombinant fragment of human CD4

CD4 glycoprotein on the surface of T cells helps in the immune response and is the receptor for HIV infection. The structure of a soluble fragment of CD4 determined at 2.3 A resolution reveals that the molecule has two intimately associated immunoglobulin-like domains. Residues implicated in HIV recognition by analysis of mutants and antibody binding are salient features in domain D1. Domain D2 is distinguished by a variation on the beta-strand topologies of antibody domains and by an intra-sheet disulphide bridge.     

Novel regulation and function of Src tyrosine kinase

Src tyrosine kinase is a critical signal transducer that modulates a wide variety of cellular functions. Misregulation of Src leads to cell transformation and cancer. Heterotrimeric guanine-nucleotide-binding proteins (G proteins) are another group of signaling molecules that transduce signals from cell-surface receptors to generate physiological responses. Recently, it was discovered that Gαs and Gαi could directly stimulate Src family tyrosine kinase activity. This novel regulation of Src tyrosine kinase by G proteins provides insights into the adenylyl cyclase-independent signaling mechanisms involved in ligand-induced receptor desensitization, internalization and other physiological processes. Received 17 August 2001; received after revision 22 October 2001; accepted 24 October 2001