TLE (temporal lobe epilepsy) is a common epilepsy syndrome with a complex etiology. Despite evidence for the participation of genetic factors, the genetic basis of TLE remains largely unknown.
This study identified a mutation in the galanin-encoding gene (GAL) which suggests that a mutation in GAL could impair galanin signaling in the hippocampus, leading to increased glutamatergic excitation and ultimately to temporal lobe epilepsy (TLE). This supports GAL as the causal gene for the temporal lobe epilepsy in the studied family.
A part of the study involved the synthesis of the 30 amino acid galanin peptides, hGal(WT) and hGal(A39E), which were used in galanin receptor binding assays. The results of this study further strengthen the role of galanin in epilepsy and could potentially have direct implications for the development of anti-epileptic treatments.
Figure 1. Galanin peptides synthesized.
New Findings presented at ASMS 2018
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