Secrets of an important byproduct revealed

At Bachem, technological leadership and strong innovation have been the cornerstones of our success since the very beginning of our company. We strive for technology and highest quality of our products. Investing in research in order to constantly improve our manufacturing process is one of our driving forces. In this context, we have studied and provided further optimized tools for one of the most widely used strategies for the covalent modification of peptides and proteins, the thiol-maleimide reaction.

In this chemical modification reaction, however, side-reactions occur and are challenging to address. Thiazine formation during the conjugation of N-terminal cysteine peptides to maleimides is one of them, and has been revealed to be underreported in peptide literature.

Scheme 1 – Thiazine rearrangement during thiol-maleimide coupling

Thiazine occurs from a side-reaction with an unprotected N-terminal cysteine

The thiol-maleimide reaction is used to add chemical labels onto biomolecules via thiol conjugation such as fluorescent dyes, PEG, radiolabels and small molecules. The advantages of this reaction are the rapid reaction speed between maleimides and thiols and the preferential chemical reaction at a neutral pH. However, various side-reactions are possible during thiol-maleimide conjugation, including thiazine rearrangement. These side-reactions are possibly explained by the instability of the maleimide-cysteine conjugate.

We have published a new study in the Journal of Peptide Science about thiazine rearrangement. Formation of the thiazine impurity (Scheme 1) can complicate the purification, characterization and storage of peptide conjugates leading to loss of product. This is why it is so important to investigate the mechanism. This study aimed to better understand this side-reaction and to develop tools that will prevent its formation. The thiazine side-reaction occurs during the conjugation of a maleimide with an unprotected N-terminal cysteine amino acid and leads to a thiazine derivative.

Scheme 2 – Structure of Succinimidyl Thioether and Thiazine impurity

For peptides that are conjugated to maleimides through an N-terminal cysteine, the resulting succinimide is susceptible to nucleophilic attack from the N-terminal amine of the cysteine. This nucleophilic attack can occur at the carbonyl at Position 1 or the carbonyl at Position 3 (Scheme 2). Transcyclization occurs through a fused bicyclic tetrahedral intermediate, which allows for the formation of a six-membered thiazine product.

Scheme 3 – Mechanism of the Thiazine formation

 
As you can see in scheme 2, the thiazine side reaction is formed after nucleophilic attack of N-terminal amine at the carbonyl of the succinimide leading to the intermediate product. Then a trancyclization occurs to give a six-membered ring product.

Protonation of the N-terminal amino group prevents the formation of thiazine impurities

To investigate wether or not this reaction is general, we studied the pH dependence and the sequence dependence of succinimidyl thioether to thiazine side-reaction using a tripeptide model system.

We observed a significant increase in the rate of thiazine formation at basic pH, which was consistent with previous work indicating that the rearrangement is promoted under basic conditions. The considerable increase in the rate of thiazine formation at higher pH supports a base-dependent mechanism involving nucleophilic attack of the succinimide by the N-terminal amine.

Then, when the amino acid adjacent to the N-terminal cysteine was substituted for various amino acids, we observed generation of the thiazine impurity in all instances, though the rates of thiazine formation differed for the tripeptides that were studied. Even using a maleimide linker that we anticipated to be more stable resulted in substantial thiazine formation, which provides additional support that the side reaction is general. The presence of thiazine has been confirmed through different analytical method.

In addition, we successfully proved that the protonation of the N-terminal amino group under acidic conditions prevents the nucleophilic reaction and therefore the formation of thiazine impurities. Even though performing conjugation under acidic conditions near pH 5 prevents thiazine formation, the subsequent purification, storage and application of the peptide conjugates needs to be performed under acidic conditions to avoid loss of succinimidyl thioether. Alternatively, acetylation of the N-terminal cysteine can be performed to prevent formation of the thiazine impurity. Regarding the general nature of the thiazine side reaction, we advise to avoid the use of N-terminal cysteine in peptide conjugates, where the succinimidyl thioether linkage is desired.

This is an exciting and novel result, which is important to keep in mind if you work with peptides, peptide-dyes, conjugates and peptide-payload conjugates, and is important for the production of peptide active pharmaceutical ingredients (APIs), used in drugs helping patients worldwide. If you would like to find out more about this interesting research, read the full journal publication.

If you want to learn even more on how to address the thiazine side-reaction, discover our webinar video: