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648931e174

When I see you I want to know you want you (going to your house) (going to your house) (going to your house) I’ll be waiting for youCarnitine and acetylcarnitine: a new synthetic route.
We report a new synthetic method for the preparation of carnitine and acetylcarnitine starting from the amino acids lysine and acetyl-L-lysine, respectively. The key step of the method involves the use of cyanuric chloride in a reaction with N-acetylated amino acid esters which are readily available in a one-step reaction from the N-acetyl amino acids. Cyanuric chloride reacts in excellent yield with N-acetyl-L-lysine to produce the corresponding N-acetylcholinester (acetylated choline) which was not previously available in good yields. The method is quite general and could be adapted to the synthesis of other N-acetyl derivatives as well as other N-protected derivatives in order to facilitate the synthesis of analogues of carnitine and acetylcarnitine.The long-term objective is to identify mechanisms by which the specific entry sequence of reovirus is recognized by receptors on host cells in order to promote reovirus uncoating and the subsequent initiation of virus transcription, replication and assembly. The specific aim is to determine how reovirus sigmaC coat protein functions within the context of the assembled virus particle. The experimental focus is on (1) the entry of reovirus into epithelial cells;(2) the role of reovirus sigmaC in virus entry;and (3) the structure of reovirus sigmaC. The sigmaC coat protein is encoded in the middle segment of the genome and is thought to mediate the attachment of the virus particle to the surface of infected cells. It has been shown that infected cells grow with a decreased overall growth rate, alter cell morphology and possess a ‘fried egg appearance’. Our hypothesis is that sigmaC provides receptors for reovirus attachment to the surface of infected cells. In an effort to identify virus receptors on non-permissive cells, cholera toxin subunit B-succinylated was fused to sigmaC. The results demonstrate that these cholera toxin subunits are capable of binding reovirus to the surface of cells. We propose to use reovirus attachment as a tool to purify the receptors.

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