インデックス付き
  • Jゲートを開く
  • Genamics JournalSeek
  • ウルリッヒの定期刊行物ディレクトリ
  • レフシーク
  • 研究ジャーナル索引作成ディレクトリ (DRJI)
  • ハムダード大学
  • エブスコ アリゾナ州
  • OCLC-WorldCat
  • プロクエスト召喚
  • 学者の舵取り
  • パブロン
  • ジュネーブ医学教育研究財団
  • ユーロパブ
  • Google スカラー
このページをシェアする
ジャーナルチラシ
Flyer image

概要

Chemical Synthesis of the Highly Hydrophobic Antiviral Membrane-protein

Monika Johnson

Solid part amide synthesis (SPPS) provides the likelihood to with chemicals synthesize peptides and proteins. Applying the strategy on hydrophilic structures is typically while not major drawbacks however face extreme complications once it involves “difficult sequences.” These include the vitally necessary, ubiquitously gift and structurally tight membrane proteins and their practical elements, like particle channels, G-protein receptors, and different pore-forming structures. Commonplace artificial and ligature protocols don't seem to be enough for a undefeated synthesis of those difficult sequences. During this review we tend to highlight, summarize and judge the probabilities for artificial production of “difficult sequences” by SPPS, native chemical ligature (NCL) and follow-up protocols. Interferon

免責事項: この要約は人工知能ツールを使用して翻訳されており、まだレビューまたは確認されていません