Scientific glossary · Pharmacology

What are albumin binding and DAC in a peptide?

Some peptides are designed to bind to blood albumin, which shields them and releases them gradually. DAC (Drug Affinity Complex) is one of those strategies.

Albumin is the most abundant plasma protein and has a half-life of about three weeks. A small peptide bound to it is protected: it is not filtered by the kidney and enzymes reach it with difficulty. It works as a circulating depot.

There are two ways to achieve that binding. The non-covalent, reversible one, through a fatty-acid chain (the lipidation of semaglutide or tirzepatide). And the covalent one, which is that of DAC: a reactive group (maleimide) attached to the peptide through a spacer, which forms a stable bond with a free cysteine on albumin.

CJC-1295 with DAC is the classic example: the same base sequence as Mod GRF 1-29, but with the affinity complex, which takes its half-life from minutes to several days. The pharmacodynamic consequence is important: it goes from a brief, pulsatile signal to sustained exposure.

Why it matters in peptide research

When “CJC-1295 with DAC” and “without DAC” are compared, these are not two brands of the same product: they are two different pharmacological profiles. The product name should always state which one it is.

Related terms

Learn it in depth at the Peptide University

Related catalogue compounds

Definition for educational and scientific purposes. It is not medical advice or a recommendation for use. NeoPeptidos products are sold labelled for research use only (RUO).