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. 2020 May 5;8:396. doi: 10.3389/fchem.2020.00396

Peptidyl ω-Asp Selenoesters Enable Efficient Synthesis of N-Linked Glycopeptides

Jing-Jing Du 1,†, Lian Zhang 1,†, Xiao-Fei Gao 2, Hui Sun 3, Jun Guo 1,*
PMCID: PMC7232547  PMID: 32478036

Abstract

Chemical synthesis is an attractive approach allows for the assembly of homogeneous complex N-linked glycopeptides and glycoproteins, but the limited coupling efficiency between glycans and peptides hampered the synthesis and research in the related field. Herein we developed an alternative glycosylation to construct N-linked glycopeptide via efficient selenoester-assisted aminolysis, which employs the peptidyl ω-asparagine selenoester and unprotected glycosylamine to perform rapid amide-bond ligation. This glycosylation strategy is highly compatible with the free carboxylic acids and hydroxyl groups of peptides and carbohydrates, and readily available for the assembly of structure-defined homogeneous N-linked glycopeptides, such as segments derived from glycoprotein EPO and IL-5.

Keywords: N-linked glycopeptide, glycosylation, selenoester, aminolysis, chemical synthesis

Introduction

Many proteins undergo co- or post-translational modifications, including phosphorylation, acetylation, and glycosylation to fulfill their functions (Walsh and Jefferis, 2006; Carubbi et al., 2019). It is estimated that glycosylation modifications are associated with approximately 50% of human proteins (Clerc et al., 2016; Oliveira-Ferrer et al., 2017) and 30% of approved biopharmaceutical proteins (Zou et al., 2020), which are critical for important biological processes in living systems, such as cell's adhesion, recognition, targeting, and differentiation (Varki, 2017; Bhat et al., 2019). Despite the importance of glycosylations, rigorous evaluation of the relationship between the precise structure and biological function of glycoproteins is complicated by the structural heterogeneity of the oligosaccharides in biological organisms, and the difficulty to obtain sufficient amounts of structure-defined glycoproteins with single glycoform from natural sources (Park et al., 2009).

In order to develop viable and efficient strategies to chemically construct homogeneous complex N-linked glycopeptides and glycoproteins, extensive efforts and advances have been made in the field (Payne and Wong, 2010; Wilson et al., 2013; Okamoto et al., 2014a; Wang and Amin, 2014; Fairbanks, 2019; Li et al., 2019), such as the resin-bound glycosylation (Kunz and Unverzagt, 1988; Vetter et al., 1995; Offer et al., 1996; Mezzato et al., 2005; Kajihara et al., 2006; Yamamoto et al., 2008; Piontek et al., 2009a,b; Chen and Tolbert, 2010; Conroy et al., 2010; Ullmann et al., 2012; Okamoto et al., 2014b; Reif et al., 2014; Lee et al., 2016; Schöwe et al., 2019) and solution glycosylation (Anisfeld and Lansbury, 1990; Cohen-Anisfeld and Lansbury, 1993; Kaneshiro and Michael, 2006; Wang et al., 2011, 2012, 2013; Aussedat et al., 2012; Nagorny et al., 2012; Sakamoto et al., 2012; Joseph et al., 2013; Chai et al., 2016; Schöwe et al., 2019). However, unneglectable limitations still remain in these strategies. Consumption of large amount of precious materials and low coupling yields usually occurred for the glycopeptide assembly on-resin via either the stepwise (Scheme 1A) or the convergent (Scheme 1B) strategy. Based on the aspartylation technology pioneered by Lansbury and co-workers (Scheme 1C) (Anisfeld and Lansbury, 1990; Cohen-Anisfeld and Lansbury, 1993), Danishefsky group and Unverzagt group developed the synthetic methods and optimized the pseudoproline dipeptide building block to construct the peptide fragement at the site of Asn-Xaa-Ser/Thr, and this approach significantly suppressed the formation of aspartimide byproducts during glycosylation (Ullmann et al., 2012; Wang et al., 2012). Although useful, requirement for additional metal catalysts or protected C-terminal carboxylic acid derivatives may limit the application of this strategy in glycopeptide assembly.

Scheme 1.

Scheme 1

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Effective strategies for chemical construction of N-linked glycopeptides: (A) stepwise strategy via solid-phase; (B) convergent strategy via solid-phase; (C) convergent strategy via solution phase.

Notwithstanding substantial advances have been made in N-linked glycopeptides and glycoproteins synthesis, it is still a great challenge to efficiently achieve large N-linked gylcoproteins bearing complex glycan forms. The desired synthetic methods will have fewer protecting groups and modifications on the peptide and glycan fragments, and promote efficient and selective ligation reactions between fragments. Previously, our research group has developed a strategy for the convergent synthesis of N-linked glycopeptides via peptidyl ω-Asp p-nitrophenyl thioester-assisted glycosylation (Scheme 1C) (Du et al., 2016). This convergent strategy with direct aminolysis provides an access to complex N-linked glycopeptides, usually with good yields and simple operation, and is worthy of further investigating more reactions and applications.

Many investigators have proved that coupling of peptide fragments via direct aminolysis is a feasible method for preparation of peptides and glycopeptides. This method employs direct coupling reaction between peptide fragments bearing N-terminal free amines and peptide fragments bearing C-terminal active esters, such as oxoesters (Kemp and Vellaccio, 1975; Wan et al., 2008; Li et al., 2010), thioesters (Payne et al., 2008; Agrigento et al., 2014; LingáTung and Clarence, 2015; Gui et al., 2016) or selenoester derivatives (Grieco et al., 1981; Mitchell et al., 2015; Raj et al., 2015; Takei et al., 2017; Temperini et al., 2017; Du et al., 2018; Sayers et al., 2018a,b; Chisholm et al., 2020; Wang et al., 2020), eliminates the need for N-terminal cysteine residues or thiol ligation auxiliaries, which are generally required for the sequential native chemical ligation (Dawson et al., 1994; Kent, 2009). Notably, the active selenoesters or derivatives always offer enhanced reactivity compared to the thio- or oxoesters (Mitchell et al., 2015; Raj et al., 2015; Takei et al., 2017). Our previous studies have shown that the aminolysis of peptidyl selenoester is an efficient strategy for peptide and glycopeptide assembly (Yin et al., 2016; Du et al., 2018). Herein we are interested in pursuing a highly reactive peptidyl ω-Asp selenoester-assisted glycosylation methodology for constructing N-linked glycopeptides without coupling reagents (Scheme 1C). This methodology is assumed to be compatible with free carboxylic groups and hydroxyl groups of peptides and glycans.

Results and Discussion

Evaluation of the Reactivity of the Active Esters for Glycosidic Amide Bond Formation

To evaluate the methods for synthesizing N-linked glycopeptide synthesis via active ester-assisted aminolysis (Du et al., 2016), the activity and efficiency of different active esters were compared and investigated using model reactions, in which Fmoc-Gly ester 2 and glycosylamine 1a (Likhosherstov et al., 1986; Cohen-Anisfeld and Lansbury, 1993) were condensed in DMSO to form β-anomer product 3 and monitored by HPLC (Table 1, Figure 1).

Table 1.

Optimization of the active esters for the glycosylation reactiona.

graphic file with name fchem-08-00396-i0001.jpg
Entry Ester X R1 R2 Time (h)b Yield (%)c
1 2a O H H >40 <1
2 2b S H H >40 8
3 2c S NO2 H 10 75
4 2d Se H H 2 92
5 2e Se H CHO 1 69
6 2f Se CHO H 1 67
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a

Reaction conditions: 1a (10 μmol), esters (5 μmol) and DIPEA (10 μmol) in 1 mL of DMSO, rt.

b

Consumption of >95% of the starting ester in glycosylation reaction was determined by HPLC.

c

Determined by HPLC at 40 h.

Figure 1.

Figure 1

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Reaction curves (yields of 3 vs. time) of the glycosidic linkage formation between 2a−2f and 1a.

For oxoester 2a, it has the lowest activity and almost no product was observed (Table 1, entry 1). For thioesters (Table 1, entries 2-3), phenyl thioester 2b underwent glycosidic bond formation slightly faster than the oxoester 2a, but it is not efficient enough to be applied in the N-linked glycopeptide synthesis; p-nitrophenyl thioester 2c with a strong electron-withdrawing group reacts more efficiently, providing the target product in a yield of 75% within 10 h, which is consistent with previous studies (Hondal et al., 2001; Du et al., 2016). Therefore, the peptidyl p-nitrophenyl thioester has been successfully utilized to prepare N-linked glycopeptide in our lab (Du et al., 2016).

To improve the efficiency of glycosylation reaction, various selenoesters were assessed under the same conditions (Table 1, entries 4–6). For seleno-phenyl ester 2d, it underwent complete conversion within 2 h, and afforded the target product 3 in 92% yield; for seleno-benzaldehyde esters 2e with the o-benzaldehyde group and 2f with the p-benzaldehyde group (Raj et al., 2015), they underwent complete conversion in <1 h, and gave the products in yield of 69 and 67%, respectively. We postulate that the participation of o-benzaldehyde (neighbor-participating group) and p-benzaldehyde, which both have electron-withdrawing groups can increase the phenyl selenoester's electrophile reaction rate, but also facilitate the hydrolysis reaction and reduce the yield of aminolysis product. Therefore, the seleno-phenyl ester 2d affords an optimal balance between high reactivity and sufficient stability, will be appropriate for the selenoester-assisted aminolysis in glycosylation reactions.

As shown in Table 2, we compared the reaction kinetic data p-nitrophenyl thioester 2c and seleno-phenyl ester 2d. As expected, the glycosylation reaction for the product 3 between glycine-derived ester and glycosylamine follows a second-order kinetics, with a rate constant 0.0071 ± 0.0004 M−1 s−1 for 2c and 0.0420 ± 0.0012 M−1 s−1 for 2d, respectively. The seleno-phenyl ester is roughly 6-times faster than the p-nitrophenyl thioester to form the glycosidic amide bond.

Table 2.

Kinetic studies for glycosidic bond formationa.

graphic file with name fchem-08-00396-i0002.jpg
Ester X R1 R2 K [M−1s−1] Relative rates
2c S NO2 H 0.0071 ± 0.0004 1
2d Se H H 0.0420 ± 0.0012 6
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a

Reaction conditions: 1a (10 μmol), esters (5 μmol) and DIPEA (10 μmol) in 1 mL of DMSO, rt.

Condition Optimization

As depicted in Table 3, various glycosylation reaction conditions were evaluated for further optimization. From the results of optimizing the solvent (Table 3, entries 1–4), the efficiency of the glycosylation reaction was shown to be greatly boosted in DMSO, but the aqueous solution of NMP/PB is prone to decompose the seleno-phenyl ester 2d. The amounts of DIPEA from 0.1 to 3.0 equivalents didn't significantly influence the yields (Table 3, entries 4–7). Additionally, we found that the product 3 was achieved in optimal yield when seleno-phenyl ester 2d was treated with 2.0 equivalents of glycosylamine 1a (Table 3, entries 4, 8–9). In order to maximize the glycosylation and minimize the hydrolysis, we selected the optimum conditions, i.e., 2.0 equivalents of DIPEA and glycosylamine 1a, and 1.0 equivalent of seleno-phenyl ester 2d were dissolved in DMSO.

Table 3.

Reaction optimization and control experimentsa.

graphic file with name fchem-08-00396-i0003.jpg
Entry 1a (equiv.) 2d (equiv.) Solvent DIPEA (equiv.) Yield (%)b
1 2 1 NMP/PB 2 52
2 2 1 NMP 2 78
3 2 1 DMF 2 76
4 2 1 DMSO 2 92
5 2 1 DMSO 3 90
6 2 1 DMSO 1 88
7 2 1 DMSO 0.1 85
8 1 1 DMSO 2 70
9 3 1 DMSO 2 93
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a

Reaction conditions: 1a (5-15 μmol), ester 2d (5 μmol) and DIPEA (10 μmol) in 1mL of solvent, rt.

b

Determined by HPLC at 2 h. PB = phosphate buffer (pH 7.4, 0.2 M).

Substrate Scope

To explore the universal applicability of selenoester-assisted glycosylation, we embarked on the attachment of seleno-phenyl esters to a series of peptides to assemble peptidyl ω-Asp selenoester substrates, and examined substrates that incorporating the free C-terminal carboxylic groups and unprotected glycosylamines. A series of partially protected peptides bearing selenoesters at the ω-aspartyl terminus (including pseudoproline dipeptides that suppress aspartimide formation) were successfully prepared for evaluation (Ullmann et al., 2012; Wang et al., 2012). These peptide substrates were conducted via stepwise solid-phase peptide synthesis (SPPS), the general synthetic procedures for 4b-12b are outlined in Figure 2 (more details are shown in the Supporting Information). The installation of phenyl selenoester group at the ω-aspartyl terminus is straightforward on the resin: firstly, the allyl esters were removed; subsequently, the ω-aspartyl carboxyl groups were converted to selenoesters (4a-12a); finally, these peptidyl selenoesters were cleaved from the resin. The ω-aspartyl selenoester peptide substrates (4b-12b) were isolated via reverse-phase HPLC purification in 58–83% yields. In addition, the glycosylamines (Figure 3) for the study are monosaccharide 1a, chitobiose 1b and undecasaccharide 1c (extracted from fresh egg yolks) (Seko et al., 1997; Sun et al., 2014).

Figure 2.

Figure 2

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Solid-phase synthesis of peptidyl selenoesters 4b-12b.

Figure 3.

Figure 3

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Structures of glycosylamines 1a-1c.

With peptidyl selenoesters and glycosylamines in hand, the glycosylation reactions at the site of natural ω-asparagine linkage were evaluated. On the one hand, the coupling of monosaccharide 1a and peptides 4b-6b gave glycosylated peptides 4c-6c in approximately 69%-83% isolated yields (Table 4, entries 1–3), proving the feasibility of utilizing unprotected glycosylamines together with peptidyl selenoesters bearing free C-terminal carboxylic groups in glycosylation reactions. To our delight, peptide 7b containing two ω-asparagine selenoesters, still gave an isolated yield of 80% of product 7c derived from multiply glycosylated protein erythropoietin (EPO; fragment 22–43) (Park et al., 2009; Wang et al., 2013; Wilson et al., 2013) with two glycosylation modifications (Table 4, entry 4). On the other hand, this strategy also afforded good results for glycosylation of disaccharides. As shown in entries 5–7, coupling of chitobiose 1b and peptidyl selenoesters 5b, 8b, and 9b formed glycosidic bond at ω-asparagine residue with excellent yields.

Table 4.

Scope of the peptidyl selenoester-based glycosylationa.

Entry Peptide + glycan ratio (P:G) Product Isolated yield
graphic file with name fchem-08-00396-i0004.jpg
1 4b + 1a
(1:2)		 graphic file with name fchem-08-00396-i0005.jpg 69%
2 5b + 1a
(1:2)		 graphic file with name fchem-08-00396-i0006.jpg 83%
3 6b + 1a
(1:2)		 graphic file with name fchem-08-00396-i0007.jpg 78%
4 7b + 1a
(1:2)		 graphic file with name fchem-08-00396-i0008.jpg 80%
5 5b + 1b
(1:2)		 graphic file with name fchem-08-00396-i0009.jpg 79%
6 8b + 1b
(1:2)		 graphic file with name fchem-08-00396-i0010.jpg 82%
7 9b + 1b
(1:2)		 graphic file with name fchem-08-00396-i0011.jpg 84%
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a

Reaction conditions: 1a (10 μmol), selenoester peptides (5 μmol) and DIPEA (10 μmol) in 1 mL of DMSO, rt, 2 h.

For this methodology, it is noteworthy that the desired N-linked glycopeptides are synthesized rapidly only through mixing two substrates, without using a condensation reagent, and the workup procedure is simple. Excitingly, the free carboxylic groups of ω-aspartyl peptide segments were readily converted into peptidyl selenoesters for further condensation with various glycosylamines. Additionally, each amino acid protecting group in glycopeptide can be easily removed in an acidic environment.

Syntheses of N-Linked Glycopeptides With Complex-Type Oligosaccharide

As shown in Table 5, the protocol of selenoester-mediated glycopeptide synthesis is extended to complex-type oligosaccharide amines. Given the structural complexity of the precious undecasaccharide amine 1c, an excessive amount of peptidyl selenoester (1.5:1) was used, and the final products (10e, 11e, 12e) of the peptides modified with undecasaccharides were achieved in good yields of 59–65% (Table 5, entries 1–3). Specially, product 12e corresponds to the truncated segment of the glycoprotein found in human interleukin-5 (IL-5, an eosinophil chemotactic factor, fragment 26–43) (Coffman et al., 1989; Liu and Dong, 2018).

Table 5.

Selenoester-mediated glycosylationa.

Entry Peptide + glycan ratio (P:G) Product Isolated yield
graphic file with name fchem-08-00396-i0012.jpg
1 10b + 1c
(1:1.5)		 graphic file with name fchem-08-00396-i0013.jpg 65%
2 11b + 1c
(1:1.5)		 graphic file with name fchem-08-00396-i0014.jpg 59%
3 12b + 1c
(1:1.5)		 graphic file with name fchem-08-00396-i0015.jpg 62%
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a

Reaction conditions: 1c (3 μmol), 10b-12b (2 μmol), DIPEA (4 μmol) in 0.5 mL of DMSO, 4 Å MS, rt, 6 h.

Conclusion

In this work we have developed a convergent and facile synthetic methodology to construct homogeneous N-linked glycopeptides from the peptides with ω-Asp phenyl selenoester, the use of peptidyl selenoesters has the merits of simple operation and obtained excellent yields of N-linked glycopeptides, such as truncated segments derived from glycoprotein EPO or IL-5. This selenoester-mediated glycosylation provides several advantages: the reactivity of the peptide ester is improved, the complex sialyloligosaccharide in its native form without protection, it is not only compatible with free C-terminal carboxylic acid groups, but also rapidly forms glycosidic bond without additional coupling reagents or catalysts. This method will be further applied to the formation of homogenous N-linked glycopeptides and glycoproteins with therapeutic potential.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation, to any qualified researcher.

Author Contributions

JG conceived the project. J-JD, LZ, and X-FG designed and performed the experiments. All authors discussed the results and commented on the manuscript.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Footnotes

Funding. The project was funded by the National Natural Science Foundation of China (Nos. 21772056 and 81670531), the National Key Research and Development Program of China (No. 2017YFA0505200), Program of Introducing Talents of Discipline to Universities of China (111 program, B17019), and the Research Fund of East China University of Technology (No. DHBK2017114).

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fchem.2020.00396/full#supplementary-material

Click here for additional data file. (2.1MB, PDF)

References

  1. Agrigento P., Albericio F., Chamoin S., Dacquignies I., Koc H., Eberle M. (2014). Facile and mild synthesis of linear and cyclic peptides via thioesters. Org. Lett. 16, 3922–3925. 10.1021/ol501669n [DOI] [PubMed] [Google Scholar]
  2. Anisfeld S. T., Lansbury P. T. (1990). A convergent approach to the chemical synthesis of asparagine-linked glycopeptides. J. Org. Chem. 55, 5560–5562. 10.1021/jo00308a009 [DOI] [Google Scholar]
  3. Aussedat B., Fasching B., Johnston E., Sane N., Nagorny P., Danishefsky S. J. (2012). Total synthesis of the α-subunit of human glycoprotein hormones: toward fully synthetic homogeneous human follicle-stimulating hormone. J. Am. Chem. Soc. 134, 3532–3541. 10.1021/ja2111459 [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bhat A. H., Maity S., Giri K., Ambatipudi K. (2019). Protein glycosylation: sweet or bitter for bacterial pathogens? Crit. Rev. Microbiol. 45, 82–102. 10.1080/1040841x.2018.1547681 [DOI] [PubMed] [Google Scholar]
  5. Carubbi F., Alunno A., Gerli R., Giacomelli R. (2019). Post-translational modifications of proteins: novel insights in the autoimmune response in rheumatoid arthritis. Cells 8:657. 10.3390/cells8070657 [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Chai H., Le Mai Hoang K., Vu M. D., Pasunooti K., Liu C.-F., Liu X.-W. (2016). N-linked glycosyl auxiliary-mediated native chemical ligation on aspartic acid: application towards N-glycopeptide synthesis. Angew. Chem. Int. Ed. 55, 10363–10367. 10.1002/anie.201605597 [DOI] [PubMed] [Google Scholar]
  7. Chen R., Tolbert T. J. (2010). Study of on-resin convergent synthesis of N-linked glycopeptides containing a large high mannose N-linked oligosaccharide. J. Am. Chem. Soc. 132, 3211–3216. 10.1021/ja9104073 [DOI] [PubMed] [Google Scholar]
  8. Chisholm T. S., Kulkarni S. S., Hossain K. R., Cornelius F., Clarke R. J., Payne R. J. (2020). Peptide ligation at high dilution via reductive diselenide-selenoester ligation. J. Am. Chem. Soc. 142, 1090–1100. 10.1021/jacs.9b12558 [DOI] [PubMed] [Google Scholar]
  9. Clerc F., Reiding K. R., Jansen B. C., Kammeijer G. S., Bondt A., Wuhrer M. (2016). Human plasma protein N-glycosylation. Glycoconj. J. 33, 309–343. 10.1007/s10719-015-9626-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Coffman R. L., Seymour B. W., Hudak S., Jackson J., Rennick D. (1989). Antibody to interleukin-5 inhibits helminth-induced eosinophilia in mice. Science 245, 308–310. 10.1126/science.2787531 [DOI] [PubMed] [Google Scholar]
  11. Cohen-Anisfeld S. T., Lansbury P. T. (1993). A practical, convergent method for glycopeptide synthesis. J. Am. Chem. Soc. 115, 10531–10537. 10.1021/ja00076a010 [DOI] [Google Scholar]
  12. Conroy T., Jolliffe K. A., Payne R. J. (2010). Synthesis of N-linked glycopeptides via solid-phase aspartylation. Org. Biomol. Chem. 8, 3723–3733. 10.1039/c003673k [DOI] [PubMed] [Google Scholar]
  13. Dawson P. E., Muir T. W., Clark-Lewis I., Kent S. B. H. (1994). Synthesis of proteins by native chemical ligation. Science 266, 776–779. 10.1126/science.7973629 [DOI] [PubMed] [Google Scholar]
  14. Du J.-J., Gao X.-F., Xin L.-M., Lei Z., Liu Z., Guo J. (2016). Convergent synthesis of N-linked glycopeptides via aminolysis of ω-Asp p-nitrophenyl thioesters in solution. Org. Lett. 18, 4828–4831. 10.1021/acs.orglett.6b02288 [DOI] [PubMed] [Google Scholar]
  15. Du J.-J., Xin L.-M., Lei Z., Zou S.-Y., Xu W.-B., Wang C.-W., et al. (2018). Glycopeptide ligation via direct aminolysis of selenoester. Chin. Chem. Lett. 29, 1127–1130. 10.1016/j.cclet.2018.04.016 [DOI] [Google Scholar]
  16. Fairbanks A. J. (2019). Chemoenzymatic synthesis of glycoproteins. Curr. Opin. Chem. Biol. 53, 9–15. 10.1016/j.cbpa.2019.05.015 [DOI] [PubMed] [Google Scholar]
  17. Grieco P. A., Jaw J. Y., Claremon D., Nicolaou K. (1981). N-Phenylselenophthalimide. A useful reagent for the facile transformation of (1) carboxylic acids into either selenol esters or amides and (2) alcohols into alkyl phenyl selenides. J Org Chem. 46, 1215–1217. 10.1021/jo00319a037 [DOI] [Google Scholar]
  18. Gui Y., Qiu L., Li Y., Li H., Dong S. (2016). Internal activation of peptidyl prolyl thioesters in native chemical ligation. J. Am. Chem. Soc. 138, 4890–4899. 10.1021/jacs.6b01202 [DOI] [PubMed] [Google Scholar]
  19. Hondal R. J., Nilsson B. L., Raines R. T. (2001). Selenocysteine in native chemical ligation and expressed protein ligation. J. Am Chem. Soc. 123, 5140–5141. 10.1021/ja005885t [DOI] [PubMed] [Google Scholar]
  20. Joseph R., Dyer F. B., Garner P. (2013). Rapid formation of N-glycopeptides via cu(II)-promoted glycosylative ligation. Org. Lett. 15, 732–735. 10.1021/ol302961s [DOI] [PubMed] [Google Scholar]
  21. Kajihara Y., Yoshihara A., Hirano K., Yamamoto N. (2006). Convenient synthesis of a sialylglycopeptide-thioester having an intact and homogeneous complex-type disialyl-oligosaccharide. Carbohydr. Res. 341, 1333–1340. 10.1016/j.carres.2006.04.037 [DOI] [PubMed] [Google Scholar]
  22. Kaneshiro C. M., Michael K. (2006). A convergent synthesis of N-glycopeptides. Angew. Chem. Int. Ed. 45, 1077–1081. 10.1002/anie.200502687 [DOI] [PubMed] [Google Scholar]
  23. Kemp D., Vellaccio F., Jr, (1975). Rapid intramolecular acyl transfer from phenol to carbinolamine. Progress toward a new class of peptide coupling reagent. Org. Chem. 40, 3003–3004. 10.1021/jp3083858 [DOI] [PubMed] [Google Scholar]
  24. Kent S. B. H. (2009). Total chemical synthesis of proteins. Chem. Soc. Rev. 38, 338–351. 10.1039/b700141j [DOI] [PubMed] [Google Scholar]
  25. Kunz H., Unverzagt C. (1988). Protecting-group-dependent stability of intersaccharide bonds-synthesis of a fucosyl-chitobiose glycopeptide. Angew. Chem. Int. Ed. 27, 1697–1699. 10.1002/anie.198816971 [DOI] [Google Scholar]
  26. Lee C. L., Liu H., Wong C. T. T., Chow H. Y., Li X. (2016). Enabling N-to-C Ser/Thr ligation for convergent protein synthesis via combining chemical ligation approaches. J. Am. Chem. Soc. 138, 10477–10484. 10.1021/jacs.6b04238 [DOI] [PubMed] [Google Scholar]
  27. Li X., Lam H. Y., Zhang Y., Chan C. K. (2010). Salicylaldehyde ester-induced chemoselective peptide ligations: enabling generation of natural peptidic linkages at the serine/threonine sites. Org. Lett. 12, 1724–1727. 10.1021/ol1003109 [DOI] [PubMed] [Google Scholar]
  28. Li Y., Tran A. H., Danishefsky S. J., Tan Z. (2019). Chemical biology of glycoproteins: From chemical synthesis to biological impact. Methods Enzymol. 621, 213–229. 10.1016/bs.mie.2019.02.030 [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Likhosherstov L. M., Novikova O. S., Derevitskaja V. A., Kochetkov N. K. (1986). A new simple synthesis of amino sugar β-D-glycosylamines. Carbohydr. Res. 146, C1–C5. 10.1016/0008-6215(86)85037-6 [DOI] [Google Scholar]
  30. LingáTung C., Clarence T. (2015). Peptide 2-formylthiophenol esters do not proceed through a Ser/Thr ligation pathway, but participate in a peptide aminolysis to enable peptide condensation and cyclization. Org. Biomol. Chem. 13, 6922–6926. 10.1039/C5OB00825E [DOI] [PubMed] [Google Scholar]
  31. Liu J., Dong S. (2018). Synthetic studies toward human interleukin-5. Chin. Chem. Lett. 29, 1131–1134. 10.1016/j.cclet.2018.05.014 [DOI] [Google Scholar]
  32. Mezzato S., Schaffrath M., Unverzagt C. (2005). An orthogonal double-linker resin facilitates the efficient solid-phase synthesis of complex-type N-glycopeptide thioesters suitable for native chemical ligation. Angew. Chem. Int. Ed. 44, 1650–1654. 10.1002/anie.200461125 [DOI] [PubMed] [Google Scholar]
  33. Mitchell N. J., Malins L. R., Liu X., Thompson R. E., Chan B., Radom L., et al. (2015). Rapid additive-free selenocystine–selenoester peptide ligation. J. Am. Chem. Soc. 137, 14011–14014. 10.1021/jacs.5b07237 [DOI] [PubMed] [Google Scholar]
  34. Nagorny P., Sane N., Fasching B., Aussedat B., Danishefsky S. J. (2012). Probing the frontiers of glycoprotein synthesis: the fully elaborated β-subunit of the human follicle-stimulating hormone. Angew. Chem. Int. Ed. 51, 975–979. 10.1002/anie.201107482 [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Offer J., Quibell M., Johnson T. (1996). On-resin solid-phase synthesis of asparagine N-linked glycopeptides: use of N-(2-acetoxy-4-methoxybenzyl) (AcHmb) aspartyl amide-bond protection to prevent unwanted aspartimide formation. J. Chem. Soc. Perkin Trans. 1, 175–182. 10.1039/P19960000175 [DOI] [Google Scholar]
  36. Okamoto R., Izumi M., Kajihara Y. (2014a). Decoration of proteins with sugar chains: recent advances in glycoprotein synthesis. Curr. Opin. Chem. Biol. 22, 92–99. 10.1016/j.cbpa.2014.09.029 [DOI] [PubMed] [Google Scholar]
  37. Okamoto R., Mandal K., Ling M., Luster A. D., Kajihara Y., Kent S. B. H. (2014b). Total chemical synthesis and biological activities of glycosylated and non-glycosylated forms of the chemokines CCL1 and Ser-CCL1. Angew. Chem. Int. Ed. 53, 5188–5193. 10.1002/anie.201310574 [DOI] [PubMed] [Google Scholar]
  38. Oliveira-Ferrer L., Legler K., Milde-Langosch K. (2017). Role of protein glycosylation in cancer metastasis. Semin. Cancer Biol. 44, 141–152. 10.1016/j.semcancer.2017.03.002 [DOI] [PubMed] [Google Scholar]
  39. Park S. S., Park J., Ko J., Chen L., Meriage D., Crouse-Zeineddini J., et al. (2009). Biochemical assessment of erythropoietin products from Asia versus US Epoetin alfa manufactured by Amgen. J. Pharm. Sci. 98, 1688–1699. 10.1002/jps.21546 [DOI] [PubMed] [Google Scholar]
  40. Payne R. J., Ficht S., Greenberg W. A., Wong C. H. (2008). Cysteine-free peptide and glycopeptide ligation by direct aminolysis. Angew. Chem. Int. Ed. 47, 4411–4415. 10.1002/anie.200705298 [DOI] [PubMed] [Google Scholar]
  41. Payne R. J., Wong C.-H. (2010). Advances in chemical ligation strategies for the synthesis of glycopeptides and glycoproteins. Chem. Commun. 46, 21–43. 10.1039/B913845E [DOI] [PubMed] [Google Scholar]
  42. Piontek C., Ring P., Harjes O., Heinlein C., Mezzato S., Lombana N., et al. (2009a). Semisynthesis of a homogeneous glycoprotein enzyme: ribonuclease C: Part 1. Angew. Chem. Int. Ed. 48, 1936–1940. 10.1002/anie.200804734 [DOI] [PubMed] [Google Scholar]
  43. Piontek C., Varón Silva D., Heinlein C., Pöhner C., Mezzato S., Ring P., et al. (2009b). Semisynthesis of a homogeneous glycoprotein enzyme: ribonuclease C: Part 2. Angew. Chem. Int. Ed. 48, 1941–1945. 10.1002/anie.200804735 [DOI] [PubMed] [Google Scholar]
  44. Raj M., Wu H., Blosser S. L., Vittoria M. A., Arora P. S. (2015). Aldehyde capture ligation for synthesis of native peptide bonds. J. Am. Chem. Soc. 137, 6932–6940. 10.1021/jacs.5b03538 [DOI] [PubMed] [Google Scholar]
  45. Reif A., Siebenhaar S., Tröster A., Schmälzlein M., Lechner C., Velisetty P., et al. (2014). Semisynthesis of biologically active glycoforms of the human cytokine interleukin 6. Angew. Chem. Int. Ed. 53, 12125–12131. 10.1002/anie.201407160 [DOI] [PubMed] [Google Scholar]
  46. Sakamoto I., Tezuka K., Fukae K., Ishii K., Taduru K., Maeda M., et al. (2012). Chemical synthesis of homogeneous human glycosyl-interferon-β that exhibits potent antitumor activity in vivo. J. Am. Chem. Soc. 134, 5428–5431. 10.1021/ja2109079 [DOI] [PubMed] [Google Scholar]
  47. Sayers J., Karpati P. M., Mitchell N. J., Goldys A. M., Kwong S. M., Firth N., et al. (2018a). Construction of challenging proline–proline junctions via diselenide–selenoester ligation chemistry. J. Am. Chem. Soc. 140, 13327–13334. 10.1021/jacs.8b07877 [DOI] [PubMed] [Google Scholar]
  48. Sayers J., Payne R. J., Winssinger N. (2018b). Peptide nucleic acid-templated selenocystine-selenoester ligation enables rapid miRNA detection. Chem. Sci. 9, 896–903. 10.1039/C7SC02736B [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Schöwe M. J., Keiper O., Unverzagt C., Wittmann V. (2019). A Tripeptide approach to the solid-phase synthesis of peptide thioacids and N-glycopeptides. Chem. Eur. J. 25, 15759–15764. 10.1002/chem.201904688 [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Seko A., Koketsu M., Nishizono M., Enoki Y., Ibrahim H. R., Juneja L. R., et al. (1997). Occurrence of a sialylglycopeptide and free sialylglycans in hen's egg yolk. Biochim. Biophys. Acta Gen. Subj. 1335, 23–32. 10.1016/S0304-4165(96)00118-3 [DOI] [PubMed] [Google Scholar]
  51. Sun B., Bao W., Tian X., Li M., Liu H., Dong J., et al. (2014). A simplified procedure for gram-scale production of sialylglycopeptide (SGP) from egg yolks and subsequent semi-synthesis of Man3GlcNAc oxazoline. Carbohydr. Res. 396, 62–69. 10.1016/j.carres.2014.07.013 [DOI] [PubMed] [Google Scholar]
  52. Takei T., Andoh T., Takao T., Hojo H. (2017). One-pot four-segment ligation using seleno- and thioesters: synthesis of superoxide dismutase. Angew. Chem. Int. Ed. 56, 15708–15711. 10.1002/anie.201709418 [DOI] [PubMed] [Google Scholar]
  53. Temperini A., Piazzolla F., Minuti L., Curini M., Siciliano C. (2017). General, mild, and metal-free synthesis of phenyl selenoesters from anhydrides and their use in peptide synthesis. J. Org. Chem. 82, 4588–4603. 10.1021/acs.joc.7b00173 [DOI] [PubMed] [Google Scholar]
  54. Ullmann V., Rädisch M., Boos I., Freund J., Pöhner C., Schwarzinger S., et al. (2012). Convergent solid-phase synthesis of N-glycopeptides facilitated by pseudoprolines at consensus-sequence Ser/Thr residues. Angew. Chem. Int. Ed. 51, 11566–11570. 10.1002/anie.201204272 [DOI] [PubMed] [Google Scholar]
  55. Varki A. (2017). Biological roles of glycans. Glycobiology 27, 3–49. 10.1093/glycob/cww086 [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Vetter D., Tumelty D., Singh S. K., Gallop M. A. (1995). A versatile solid-phase synthesis of N-linked glycopeptides. Angew. Chem. Int. Ed. 34, 60–63. 10.1002/anie.199500601 [DOI] [Google Scholar]
  57. Walsh G., Jefferis R. (2006). Post-translational modifications in the context of therapeutic proteins. Nat. Biotechnol. 24, 1241–1252. 10.1038/nbt1252 [DOI] [PubMed] [Google Scholar]
  58. Wan Q., Chen J., Yuan Y., Danishefsky S. J. (2008). Oxo-ester mediated native chemical ligation: concept and applications. J. Am Chem. Soc. 130, 15814–15816. 10.1021/ja804993y [DOI] [PMC free article] [PubMed] [Google Scholar]
  59. Wang L.-X., Amin M. N. (2014). Chemical and chemoenzymatic synthesis of glycoproteins for deciphering functions. Chem. Biol. 21, 51–66. 10.1016/j.chembiol.2014.01.001 [DOI] [PMC free article] [PubMed] [Google Scholar]
  60. Wang P., Aussedat B., Vohra Y., Danishefsky S. J. (2012). An advance in the chemical synthesis of homogeneous N-linked glycopolypeptides by convergent aspartylation. Angew. Chem. Int. Ed. 51, 11571–11575. 10.1002/anie.201205038 [DOI] [PMC free article] [PubMed] [Google Scholar]
  61. Wang P., Dong S., Shieh J.-H., Peguero E., Hendrickson R., Moore M. A. S., et al. (2013). Erythropoietin derived by chemical synthesis. Science 342, 1357–1360. 10.1126/science.1245095 [DOI] [PMC free article] [PubMed] [Google Scholar]
  62. Wang P., Li X., Zhu J., Chen J., Yuan Y., Wu X., et al. (2011). Encouraging progress in the ω-aspartylation of complex oligosaccharides as a general route to β-N-linked glycopolypeptides. J. Am. Chem. Soc. 133, 1597–1602. 10.1021/ja110115a [DOI] [PMC free article] [PubMed] [Google Scholar]
  63. Wang X., Corcilius L., Premdjee B., Payne R. J. (2020). Synthesis and utility of β-selenophenylalanine and β-selenoleucine in diselenide–selenoester ligation. J Org. Chem. 85, 1567–1578. 10.1021/acs.joc.9b02665 [DOI] [PubMed] [Google Scholar]
  64. Wilson R. M., Dong S., Wang P., Danishefsky S. J. (2013). The winding pathway to erythropoietin along the chemistry–biology frontier: a success at last. Angew. Chem. Int. Ed. 52, 7646–7665. 10.1002/anie.201301666 [DOI] [PMC free article] [PubMed] [Google Scholar]
  65. Yamamoto N., Tanabe Y., Okamoto R., Dawson P. E., Kajihara Y. (2008). Chemical synthesis of a glycoprotein having an intact human complex-type sialyloligosaccharide under the boc and fmoc synthetic strategies. J. Am. Chem. Soc. 130, 501–510. 10.1021/ja072543f [DOI] [PubMed] [Google Scholar]
  66. Yin X.-G., Gao X.-F., Du J.-J., Zhang X.-K., Chen X.-Z., Wang J., et al. (2016). Preparation of protein conjugates via homobifunctional diselenoester cross-linker. Org. Lett. 18, 5796–5799. 10.1021/acs.orglett.6b02568 [DOI] [PubMed] [Google Scholar]
  67. Zou Y., Hu J., Jie J., Lai J., Li M., Liu Z., et al. (2020). Comprehensive analysis of human IgG Fc N-glycopeptides and construction of a screening model for colorectal cancer. J. Proteomics 213:103616. 10.1016/j.jprot.2019.103616 [DOI] [PubMed] [Google Scholar]

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