{Reference Type}: Journal Article
{Title}: Tetrazine-trans-cyclooctene ligation: Unveiling the chemistry and applications within the human body.
{Author}: Tomarchio EG;Turnaturi R;Saccullo E;Patamia V;Floresta G;Zagni C;Rescifina A;
{Journal}: Bioorg Chem
{Volume}: 150
{Issue}: 0
{Year}: 2024 Jun 18
{Factor}: 5.307
{DOI}: 10.1016/j.bioorg.2024.107573
{Abstract}: Bioorthogonal reactions have revolutionized chemical biology by enabling selective chemical transformations within living organisms and cells. This review comprehensively explores bioorthogonal chemistry, emphasizing inverse-electron-demand Diels-Alder (IEDDA) reactions between tetrazines and strained dienophiles and their crucial role in chemical biology and various applications within the human body. This highly reactive and selective reaction finds diverse applications, including cleaving antibody-drug conjugates, prodrugs, proteins, peptide antigens, and enzyme substrates. The versatility extends to hydrogel chemistry, which is crucial for biomedical applications, yet it faces challenges in achieving precise cellularization. In situ activation of cytotoxic compounds from injectable biopolymer belongs to the click-activated protodrugs against cancer (CAPAC) platform, an innovative approach to tumor-targeted prodrug delivery and activation. The CAPAC platform, relying on click chemistry between trans-cyclooctene (TCO) and tetrazine-modified biopolymers, exhibits modularity across diverse tumor characteristics, presenting a promising approach in anticancer therapeutics. The review highlights the importance of bioorthogonal reactions in developing radiopharmaceuticals for positron emission tomography (PET) imaging and theranostics, offering a promising avenue for diverse therapeutic applications.