Preparation of radioactive ε-N-methylated lysines not involving elaborate organic synthesis

Paik, Woon Ki; DiMaria, Peter; Pearson, Earl; Kim, Sangduk

doi:10.1016/0003-2697(78)90031-3

Cited by 7 publications

References 12 publications

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Measurement of isoelectric point of S‐adenosyl‐L‐methionine and its metabolic products by an isoelectric focusing technique

1983

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The isoelectric point (pI) of S‐adenosyl‐L‐methionine and some of its metabolic products has been determined by an isoelectric focusing technique. The experimental pI values of S‐adenosyl‐L‐methionine and S‐methylmethionine are 7.24 and 6.85, respectively, and the pI values of S‐adenosyl‐L‐homocysteine and homocysteine are 6.05 and 5.65, respectively. This indicates that the contribution by adenosine, adenine and ribose to the total electric charge of S‐adenosyl‐L‐methionine or S‐adenosyl‐L‐homocysteine is approximately 0.40 pI unit. The differences in the pI values between two pairs of compounds (S‐adenosyl‐L‐methionine vs. S‐adenosyl‐L‐homocysteine and S‐methylmethionine vs. methionine) are very close (1.19 and 1.14, respectively). This difference is the amount of pI value contributed by the sulfonium group which has been formed by methyl addition. Surprisingly, the presence of a permanent positive charge at the sulfonium center in S‐adenosyl‐L‐methionine and S‐methylmethionine does not result in a higher pI values for these compounds. This might be due to the partial neutralization of the positive charge by the formation of carbanion. The mechanism of charge neutralization in these sulfonium compounds is discussed.

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