کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
10880364 | 1076960 | 2007 | 18 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Modulation of insect Cav channels by peptidic spider toxins
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کلمات کلیدی
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
بیوشیمی، ژنتیک و زیست شناسی مولکولی (عمومی)
پیش نمایش صفحه اول مقاله
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چکیده انگلیسی
Insects have a much smaller repertoire of voltage-gated calcium (CaV) channels than vertebrates. Drosophila melanogaster harbors only a single ortholog of each of the vertebrate CaV1, CaV2, and CaV3 subtypes, although its basal inventory is expanded by alternative splicing and editing of CaV channel transcripts. Nevertheless, there appears to be little functional plasticity within this limited panel of insect CaV channels, since severe loss-of-function mutations in genes encoding the pore-forming α1 subunits in Drosophila are embryonic lethal. Since the primary role of spider venom is to paralyze or kill insect prey, it is not surprising that most, if not all, spider venoms contain peptides that potently modify the activity of these functionally critical insect CaV channels. Unfortunately, it has proven difficult to determine the precise ion channel subtypes recognized by these peptide toxins since insect CaV channels have significantly different pharmacology to their vertebrate counterparts, and cloned insect CaV channels are not available for electrophysiological studies. However, biochemical and genetic studies indicate that some of these spider toxins might ultimately become the defining pharmacology for certain subtypes of insect CaV channels. This review focuses on peptidic spider toxins that specifically target insect CaV channels. In addition to providing novel molecular tools for ion channel characterization, some of these toxins are being used as leads to develop new methods for controlling insect pests.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Toxicon - Volume 49, Issue 4, 15 March 2007, Pages 513-530
Journal: Toxicon - Volume 49, Issue 4, 15 March 2007, Pages 513-530
نویسندگان
Glenn F. King,