Total Synthesis of the TIM-1 IgV Domain via N-to-C Serine/Threonine Ligation Enabled by Knorr Pyrazole Synthesis-Mediated Regeneration of Salicylaldehyde Esters.

Fuente: PubMed
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Autori principali: Cheng, Xiaolin, Sun, Zhenquan, Wu, Hongxiang, Xiao, Yisa, Shi, Pengfei, Li, Can, Zeng, Jingwen, Liu, Han, Li, Xuechen
Natura: Artículo científico
Lingua:en
Pubblicazione: Journal of the American Chemical Society 2026
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author Cheng, Xiaolin
Sun, Zhenquan
Wu, Hongxiang
Xiao, Yisa
Shi, Pengfei
Li, Can
Zeng, Jingwen
Liu, Han
Li, Xuechen
author_facet Cheng, Xiaolin
Sun, Zhenquan
Wu, Hongxiang
Xiao, Yisa
Shi, Pengfei
Li, Can
Zeng, Jingwen
Liu, Han
Li, Xuechen
Cheng, Xiaolin
Sun, Zhenquan
Wu, Hongxiang
Xiao, Yisa
Shi, Pengfei
Li, Can
Zeng, Jingwen
Liu, Han
Li, Xuechen
collection PubMed - marine biology
contents Total Synthesis of the TIM-1 IgV Domain via N-to-C Serine/Threonine Ligation Enabled by Knorr Pyrazole Synthesis-Mediated Regeneration of Salicylaldehyde Esters. Cheng, Xiaolin Sun, Zhenquan Wu, Hongxiang Xiao, Yisa Shi, Pengfei Li, Can Zeng, Jingwen Liu, Han Li, Xuechen Esters Aldehydes Pyrazoles Hepatitis A Virus Cellular Receptor 1 Threonine Serine Humans Protein Domains T-cell immunoglobulin and mucin domain-containing protein 1 (TIM-1) have recently emerged as the B-cell immune checkpoint with the potential to overcome the resistance of traditional immune checkpoint blockade therapy. However, the chemical biology of its post-translational glycosylations remains unexplored due to the absence of synthetic access to its homogeneous isoform. Here we report the total synthesis of the TIM-1 IgV-like domain (21-121) through the N-to-C Ser/Thr ligation (STL) with native chemical ligation (NCL). During the synthesis, we uncovered an unprecedented incompatibility of pyruvic acid-mediated salicylaldehyde (SAL) ester regeneration with tryptophan residues. Mechanistic studies revealed that indole side chains condense with pyruvic acid under acidic conditions, leading to side reactions. Guided by this insight, we developed an acetyl acetone (AcAc)-mediated "off-on" method that harnesses Knorr pyrazole synthesis to regenerate SAL esters with exceptional compatibility toward Trp. By combining this advance with aggregation-disrupting strategies, we achieved the first chemical synthesis of the bioactive TIM-1 IgV domain confirmed by various characterizations including high-resolution mass spectroscopy (HRMS), circular dichroism (CD) spectroscopy, and enzyme-linked immunosorbent assay (ELISA).
format Artículo científico
id pubmed_41424001
institution PubMed
language en
publishDate 2026
publisher Journal of the American Chemical Society
record_format pubmed
spellingShingle Total Synthesis of the TIM-1 IgV Domain via N-to-C Serine/Threonine Ligation Enabled by Knorr Pyrazole Synthesis-Mediated Regeneration of Salicylaldehyde Esters.
Cheng, Xiaolin
Sun, Zhenquan
Wu, Hongxiang
Xiao, Yisa
Shi, Pengfei
Li, Can
Zeng, Jingwen
Liu, Han
Li, Xuechen
Esters
Aldehydes
Pyrazoles
Hepatitis A Virus Cellular Receptor 1
Threonine
Serine
Humans
Protein Domains
Total Synthesis of the TIM-1 IgV Domain via N-to-C Serine/Threonine Ligation Enabled by Knorr Pyrazole Synthesis-Mediated Regeneration of Salicylaldehyde Esters. Cheng, Xiaolin Sun, Zhenquan Wu, Hongxiang Xiao, Yisa Shi, Pengfei Li, Can Zeng, Jingwen Liu, Han Li, Xuechen Esters Aldehydes Pyrazoles Hepatitis A Virus Cellular Receptor 1 Threonine Serine Humans Protein Domains T-cell immunoglobulin and mucin domain-containing protein 1 (TIM-1) have recently emerged as the B-cell immune checkpoint with the potential to overcome the resistance of traditional immune checkpoint blockade therapy. However, the chemical biology of its post-translational glycosylations remains unexplored due to the absence of synthetic access to its homogeneous isoform. Here we report the total synthesis of the TIM-1 IgV-like domain (21-121) through the N-to-C Ser/Thr ligation (STL) with native chemical ligation (NCL). During the synthesis, we uncovered an unprecedented incompatibility of pyruvic acid-mediated salicylaldehyde (SAL) ester regeneration with tryptophan residues. Mechanistic studies revealed that indole side chains condense with pyruvic acid under acidic conditions, leading to side reactions. Guided by this insight, we developed an acetyl acetone (AcAc)-mediated "off-on" method that harnesses Knorr pyrazole synthesis to regenerate SAL esters with exceptional compatibility toward Trp. By combining this advance with aggregation-disrupting strategies, we achieved the first chemical synthesis of the bioactive TIM-1 IgV domain confirmed by various characterizations including high-resolution mass spectroscopy (HRMS), circular dichroism (CD) spectroscopy, and enzyme-linked immunosorbent assay (ELISA).
title Total Synthesis of the TIM-1 IgV Domain via N-to-C Serine/Threonine Ligation Enabled by Knorr Pyrazole Synthesis-Mediated Regeneration of Salicylaldehyde Esters.
topic Esters
Aldehydes
Pyrazoles
Hepatitis A Virus Cellular Receptor 1
Threonine
Serine
Humans
Protein Domains
url https://pubmed.ncbi.nlm.nih.gov/41424001/