Kitahara Katsushi, Rondon Aurélie, Miller Edward, Mak Howard H, Loas Andrei, Pentelute Bradley L
Department of Chemistry, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, USA.
Present address: Sumitomo Pharma Co., Ltd., 3-1-98 Kasugade-naka, Konohana-ku, Osaka 554-0022, Japan.
bioRxiv. 2024 Aug 23:2024.08.22.609257. doi: 10.1101/2024.08.22.609257.
Peptide-based therapeutics are currently in great demand but often suffer from rapid clearance and accumulation in off-target tissues which continue to present barriers in their clinical translation. Here, we developed an electrophilic peptide for the attachment of therapeutics to native immunoglobulin (IgG) in vivo, enabling the bioorthogonal covalent linkage, or 'painting', of peptide drugs of choice to circulating IgGs directly in live animals. Native IgG painting with glucagon-like peptide-1 (GLP-1) results in sustained body weight loss and prolonged blood glucose management after one dose. Such technology might revolutionize the next generation of long-acting peptide-based medicines.
基于肽的疗法目前需求巨大,但常常因在体内快速清除以及在非靶组织中蓄积而受到影响,这在其临床转化过程中仍是障碍。在此,我们开发了一种亲电肽,用于在体内将治疗药物与天然免疫球蛋白(IgG)连接,从而能够在活体动物体内将所选肽药物与循环IgG进行生物正交共价连接,即“标记”。用胰高血糖素样肽-1(GLP-1)对天然IgG进行标记,一次给药后可导致体重持续减轻并延长血糖控制时间。这种技术可能会彻底改变下一代长效肽类药物。