Ligation of Soluble but Unreactive Peptide Segments in the Chemical Synthesis of Haemophilus Influenzae DNA Ligase. Issue 35 (25th July 2019)
- Record Type:
- Journal Article
- Title:
- Ligation of Soluble but Unreactive Peptide Segments in the Chemical Synthesis of Haemophilus Influenzae DNA Ligase. Issue 35 (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 : The surprising phenomenon of a soluble peptide segment that failed to undergo native chemical ligation was observed and attributed to the formation of soluble colloidal particles in an aqueous guanidine hydrochloride (6 m ) solution (A). A removable backbone modification strategy (B) was found to be effective for achieving the ligation of this soluble but unreactiveAbstract: 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 : The surprising phenomenon of a soluble peptide segment that failed to undergo native chemical ligation was observed and attributed to the formation of soluble colloidal particles in an aqueous guanidine hydrochloride (6 m ) solution (A). A removable backbone modification strategy (B) was found to be effective for achieving the ligation of this soluble but unreactive system. … (more)
- Is Part Of:
- Angewandte Chemie international edition. Volume 58:Issue 35(2019)
- Journal:
- Angewandte Chemie international edition
- Issue:
- Volume 58:Issue 35(2019)
- Issue Display:
- Volume 58, Issue 35 (2019)
- Year:
- 2019
- Volume:
- 58
- Issue:
- 35
- Issue Sort Value:
- 2019-0058-0035-0000
- Page Start:
- 12231
- Page End:
- 12237
- Publication Date:
- 2019-07-25
- Subjects:
- backbone modification -- DNA ligase -- mirror-image biology -- native chemical ligation -- proteins
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3773 ↗
http://www.interscience.wiley.com/jpages/1433-7851 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/anie.201905149 ↗
- Languages:
- English
- ISSNs:
- 1433-7851
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0902.000500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 14193.xml