ペプチド修飾

同位体標識ペプチド

Stable isotope labeled peptides can be useful for the determination of protein structure and dynamics or protein-protein interactions

What is Isotope Labeled Peptides?

Stable isotope labelling is a chemical reagent in which the molecules of a compound contain one or more stable isotope atoms and are analysed and determined using their unique tracer properties.

Stable isotope labelling techniques are based on the principle of labelling a reactant by replacing specific atoms with an isotope, which then causes the reactant to undergo a reaction and detects the atoms with a change in neutron number, which can be tracked by reactions, metabolic pathways or cells. Stable isotope (13C, 15N, 13C15N) labelled peptides are commonly used as ‘chemical tags’ in quantitative proteomics for the detection and tracing of biological samples. Quantitative proteomics methods mainly use high-resolution mass spectrometry to separate isotope-labelled and non-labelled peptide ions or peptide ions, and use the intensity values of their detected signals for quantitative calculations.

Stable isotope labelling technology has the advantages of high sensitivity, simple positioning and accurate quantification, which makes isotope modification get more and more widespread attention in the field of medicine and biochemistry.

同位体標識ペプチド

Precision Tools for Research

Stable isotope labeled peptides are synthesized by substituting specific atoms in natural amino acids with heavy isotopes, such as replacing 12C with 13C, 14N with 15N, or 1H with 2H (deuterium). These modifications result in isotope labeled compounds that retain the same physiochemical properties and chemical reactivity as their non-labeled counterparts. This makes them indispensable in a wide array of scientific applications, including mass spectrometry, NMR studies, and pharmacokinetic analyses.

Amino Acid
Isotope
Mass Difference to non-labeled AA

Alanine

U- 13C3, U-15N

+4 Da

Arginine

U- 13C6, U-15N4

+10 Da

Leucine

U- 13C6, U-15N

+7 Da

Lysine

U- 13C6, U-15N2

+8 Da

Phenylalanine

U- 13C9, U-15N

+10 Da

Proline

U- 13C5, U-15N

+6 Da

Valine

U- 13C5, U-15N

+6 Da

注目の引用文献

Using stable isotope labeling to advance our understanding of Alzheimer’s disease etiology and pathology

Stable isotope labeling with mass spectrometry (MS)-based proteomic analysis has become a powerful strategy to assess protein steady-state levels, protein turnover, and protein localization. Applying these analyses platforms to neurodegenerative disorders may uncover new aspects of the etiology of these devastating diseases. Recently, stable isotopes-MS has been used to investigate early pathological mechanisms of Alzheimer’s disease (AD) with mouse models of AD-like pathology. In this review, we summarize these stable isotope-MS experimental designs and the recent application in the context of AD pathology. We also describe our current efforts aimed at using nuclear magnetic resonance (NMR) analysis of stable isotope labeled amyloid fibrils from AD mouse model brains. まとめて, these methodologies offer new opportunities to study proteome changes in AD and other neurodegenerative diseases by elucidating mechanisms to target for treatment and prevention.

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改善できる可能性がある共有結合修飾です。

続きを読む

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

続きを読む

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.

続きを読む

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.

続きを読む

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.

検索 ワッツアップ サービス 製品