Ligation of Soluble but Unreactive Peptide Segments in the Chemical Synthesis of Haemophilus Influenzae DNA Ligase. (25th July 2019)
- Record Type:
- Journal Article
- Title:
- Ligation of Soluble but Unreactive Peptide Segments in the Chemical Synthesis of Haemophilus Influenzae DNA Ligase. (25th July 2019)
- Main Title:
- Ligation of Soluble but Unreactive Peptide Segments in the Chemical Synthesis of Haemophilus Influenzae DNA Ligase
- Authors:
- Zhang, Baochang
Deng, Qiang
Zuo, Chong
Yan, Bingjia
Zuo, Chao
Cao, Xiu‐Xiu
Zhu, Ting F.
Zheng, Ji‐Shen
Liu, Lei - Abstract:
- Abstract: During the total chemical synthesis of the water‐soluble globular Haemophilus Influenzae DNA ligase (Hin‐Lig), we observed the surprising phenomenon of a soluble peptide segment that failed to undergo native chemical ligation. Based on dynamic light scattering and transmission electron microscopy experiments, we determined that the peptide formed soluble colloidal particles in a homogeneous solution containing 6 m guanidine hydrochloride. Conventional peptide performance‐improving strategies, such as installation of a terminal/side‐chain Arg tag or O ‐acyl isopeptide, failed to enable the reaction, presumably because of their inability to disrupt the formation of soluble colloidal particles. However, a removable backbone modification strategy recently developed for the synthesis of membrane proteins did disrupt the formation of the colloids, and the desired ligation of this soluble but unreactive system was eventually accomplished. This work demonstrates that an appropriate solution dispersion state, in addition to good peptide solubility, is a prerequisite for successful peptide ligation. Abstract : Das überraschende Phänomen eines löslichen Peptidsegments, das keine native chemische Ligation eingehen konnte, wurde beobachtet und auf die Bildung löslicher kolloidaler Partikel in einer wässrigen Guanidinhydrochloridlösung (6 m ) zurückgeführt (A). Das Einführen einer entfernbaren Rückgratmodifikation (B) erwies sich als effektiv, um die Ligation dieses löslichen,Abstract: During the total chemical synthesis of the water‐soluble globular Haemophilus Influenzae DNA ligase (Hin‐Lig), we observed the surprising phenomenon of a soluble peptide segment that failed to undergo native chemical ligation. Based on dynamic light scattering and transmission electron microscopy experiments, we determined that the peptide formed soluble colloidal particles in a homogeneous solution containing 6 m guanidine hydrochloride. Conventional peptide performance‐improving strategies, such as installation of a terminal/side‐chain Arg tag or O ‐acyl isopeptide, failed to enable the reaction, presumably because of their inability to disrupt the formation of soluble colloidal particles. However, a removable backbone modification strategy recently developed for the synthesis of membrane proteins did disrupt the formation of the colloids, and the desired ligation of this soluble but unreactive system was eventually accomplished. This work demonstrates that an appropriate solution dispersion state, in addition to good peptide solubility, is a prerequisite for successful peptide ligation. Abstract : Das überraschende Phänomen eines löslichen Peptidsegments, das keine native chemische Ligation eingehen konnte, wurde beobachtet und auf die Bildung löslicher kolloidaler Partikel in einer wässrigen Guanidinhydrochloridlösung (6 m ) zurückgeführt (A). Das Einführen einer entfernbaren Rückgratmodifikation (B) erwies sich als effektiv, um die Ligation dieses löslichen, aber unreaktiven Systems zu erreichen. … (more)
- Is Part Of:
- Angewandte Chemie. Volume 131:Number 35(2019)
- Journal:
- Angewandte Chemie
- Issue:
- Volume 131:Number 35(2019)
- Issue Display:
- Volume 131, Issue 35 (2019)
- Year:
- 2019
- Volume:
- 131
- Issue:
- 35
- Issue Sort Value:
- 2019-0131-0035-0000
- Page Start:
- 12359
- Page End:
- 12365
- Publication Date:
- 2019-07-25
- Subjects:
- DNA-Ligase -- Native chemische Ligation -- Proteine -- Rückgratmodifikation -- Spiegelbildliche Biologie
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ange.201905149 ↗
- Languages:
- English
- ISSNs:
- 0044-8249
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0902.000000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 14192.xml