ペプチド修飾

環状ペプチド

ペプチドの環化によりペプチドの立体構造の安定性が向上します (線形類似体と比較して) これはペプチド開発における一般的な戦略です.

What is Cyclic Peptide?

Peptide cyclization to form cyclic peptides or cyclized peptides is a frequently used strategy for the development of peptides with enhanced conformational stability compared to their linear analogs. Cyclic peptides have proven to be useful for several applications, including the mimicry of protein secondary structures, such as protein loops, and the optimization of peptide ligands with increased binding potency, 選択性, and enhanced protease stability.

Cyclization configurations

The primary ligation approaches to synthesize lactam cyclic peptides are head-to-tail, サイドチェーンからサイドチェーンへ, head-to-side-chain, and side-chain-to-tail,depending on the location of the functional groups within the peptide sequence.

Head to Tail

·Occurs between N-terminus to C-terminus.
·Via Amide bond formation (lactamization).
·Most frequently used cyclization conferring greater stability.

Side Chain to Head

Occurs between N-terminus and an internal COOH
(例えば. the ß-COOH-group of Asp or γ-COOH-group of Glu).

Side Chain to tail

Occurs between internal NH2s and C-terminus
(例えば. the ε-NH2–group of Lys).

Side Chain to Side Chain

Occurs between Side chain of Lysine (ε-NH2–group of Lys) to Aspartic or Glutamic acid (γ-COOH-group).

注目の引用文献

Design and NMR Studies of Cyclic Peptides Targeting the N-Terminal Domain of the Protein Tyrosine Phosphatase YopH

We report on the design and evaluation of novel cyclic peptides targeting the N-terminal domain of the protein tyrosine phosphatase YopH from Yersinia. Cyclic peptides have been designed based on a short sequence from the protein SKAP-HOM [DE(pY)DDPF (pY = phosphotyrosine)], and they all contain the motif DEZXDPfK (where Z is a phosphotyrosine or a non-hydrolyzable phosphotyrosine mimetic, X is an aspartic acid or a leucine and f is a d-phenylalanine). These peptides present a ‘head to tail’ architecture, enabling cyclization through formation of an amide bond in between the side chains of the first aspartic acid and the lysine residues. Chemical shift perturbation studies have been carried out to monitor the binding of these peptides to the N-terminal domain of YopH. Peptides containing a phosphotyrosine moiety exhibit binding affinities in the low micromolar range; substitution of the phosphotyrosine with one of its non-hydrolyzable derivatives dramatically reduces the binding affinities. These preliminary studies may pave the way for the discovery of more potent and selective peptidebased ligands of the YopH N-terminal domain which could be further investigated for their ability to inhibit Yersiniae infections.

関連するペプチド修飾サービス

ペプチドのグリコシル化

ペプチドのグリコシル化

ペプチドのグリコシル化は、ペプチドの物理化学的特性を向上させる可能性がある共有結合修飾です。

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ペプチドのリン酸化

ペプチドのリン酸化

セリンではリン酸化が起こる可能性があります (S, であること), スレオニン (T, Thr) とチロシン (Y, ティール) リン酸エステル結合形成による側鎖

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ステープルペプチド

ステープルペプチド

α-メチルを含む2種類の非天然アミノ酸の導入, ペプチド鎖の固相合成中のα-アルケニル基.

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環状ペプチド

環状ペプチド

ペプチドの環化によりペプチドの立体構造の安定性が向上します (線形類似体と比較して) これはペプチド開発における一般的な戦略です.

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ペプチド修飾

ペプチド修飾の豊富な経験, ペプチド研究に複数の実行可能な手段を提供.

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