ʻO ka hoʻololi pololei ʻana o nā peptides i loaʻa i ka cysteine ​​a i ʻole nā ​​protein e hoʻohana ana i nā paʻakai alkylthiophenium

ʻO ka hoʻololi pololei ʻana o nā peptides i loaʻa i ka cysteine ​​a i ʻole nā ​​protein e hoʻohana ana i nā paʻakai alkylthiophenium

Bioorthogonal chemistry, as a versatile method for selective modification of biomolecules under mild physiological conditions, has attracted the attention of the scientific community in recent years due to its wide range of applications and far-reaching impact. Eia naʻe, reactive groups (e.g., alkynyl, azide, tetrazine, etc.) in conventional click chemistry are extremely rare in natural biomolecules, making the introduction of these groups a challenging task. Cysteine (Cys) is widely present in peptides and proteins, and it is estimated that about 2% of cysteine (Cys) is present in natural products.This amino acid, which is relatively abundant in proteins and is rich in thiol groups, provides an SH site for the modification of peptides and proteins, based on which an orthogonal chemical modification strategy based on alkyl thiophenium salts has been developed by the research organization.

Technical Highlights

  • Highly selective: Alkyl thiophenium salts are able to directly and selectively orthogonally modify cysteine residues via S_N2 reaction, a process that takes place under mild conditions with high chemoselectivity and compatibility.
  • Multifunctional modification: The technology is capable of introducing a wide range of functional structures, including PEG chains, fluorescent molecules, drugs, carboboranes, carbohydrates, and peptides, greatly enriching the functionality of biomolecules.
  • Multifunctional biocoupling: The study further reveals that the technology enables multifunctional biocoupling by introducing clickable “handles” such as alkynes and azides. This means that a variety of complex biocouplings can be flexibly assembled in a “two-step, one-pot” reaction, further broadening the scope of biomodification applications.
  • Successful application to proteins: The application of this technology to complex proteins has also been validated. Scientists successfully labeled bovine serum albumin (BSA) using alkylthioindigo salts, demonstrating the universality and effectiveness of the method in complex biomolecules.

The orthogonal biocoupling technique based on alkylthiophenium salts is an efficient and precise modification method, which provides a powerful tool for efficient and specific modification of peptides and proteins, and has a broad application prospect.

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Xiaoxia Chen

Laau Laau Hou R&D ʻenehana Kaʻike kumu: Loaʻa ka pahuhopu, pilina hana-hana (SAR) kālailai, peptide-lāʻau conjugates (Nā PDC), a me ka hoʻomohala ʻana i nā peptides anti-kahiko a me ka metabolic.

Pilikino: Ua alakaʻi ʻo Xiaoxia Chen i ka ʻike mua ʻana a me ka noiʻi preclinical no kekahi mau lāʻau peptide metabolic a me ka tumor-targeted.. ʻAʻole wale ʻo ia i mākaukau i ka nānā ʻana i nā hale waihona puke peptide, akā akamai nō hoʻi i ka hoʻohana ʻana i ka biology computational kōkua AI no ka hoʻolālā ʻana o ka de novo peptide sequence.. I kēia manawa, ke alakaʻi nei ʻo ia i kahi hui i hoʻolaʻa ʻia i ka noiʻi hohonu a me ka hoʻomohala ʻana o nā agonists multifunctional hanauna hou (like me pālua- a i ʻole nā ​​peptides hoʻohaʻahaʻa momona ʻekolu) a me nā peptides hoʻoponopono kino ikaika loa.

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