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HDL biology

First CETP-specific antibody fragments enable a new quantification assay and link plasma CETP to body fat mass (Clin Chem Lab Med 2004)

Original title: Phage-displayed recombinant single-chain antibody fragments with high affinity for cholesteryl ester transfer protein (CETP): cDNA cloning, characterization and CETP quantification

Clin Chem Lab Med · · 6

Ritsch A, Ebenbichler C, Naschberger E, Schgoer W, Stanzl U, Dietrich H, Heinrich PC, Saito K, Patsch JR

Researchers report the first cloning and characterization of single-chain antibody fragments specific for CETP, generated from a phage display library built from spleen mRNA of mice immunized with purified CETP. Screening yielded two high-affinity fragments, 1CL8 and 1CL10, with KD values of 4.36x10-9 M and 4.64x10-9 M, with heavy-chain complementarity-determining regions responsible for the high-affinity binding. Fragment 1CL8 was used to build a clinical chemistry CETP quantification system, which revealed an association in humans between plasma CETP concentration and total body fat mass (r=0.50, p<0.002). The authors propose these antibody fragments as powerful new tools for studying CETP's role in atherogenesis.

Read the paper (DOI)PubMed

Original abstract

Cholesteryl ester transfer protein (CETP) greatly affects the metabolism of all lipoprotein classes including low-density lipoprotein (LDL) and high-density lipoprotein (HDL), both known to constitute powerful risk factors for coronary artery disease (CAD). We now report the successful first cloning and characterization of single-chain antibody fragments specific for CETP. A recombinant phage display library was generated using spleen mRNA isolated from BALB/c mice that had been immunized with highly purified CETP. Screening of the library yielded two single-chain antibody fragments with high affinity for CETP, termed 1CL8 and 1CL10, displaying respective KD values of 4.36 x 10(-9) M and 4.64 x 10(-9) M as determined by affinity sensor technology. Amino acid sequence comparison indicated the complementarity-determining regions of the respective heavy chains to be responsible for CETP high affinity binding. Fragment 1CL8 was successfully employed in clinical chemical quantification systems that uncovered an association in humans between plasma CETP concentration and total body fat mass (r=0.50, p<0.002). Because of the demonstrated superb CETP capturing capacity, combined with high binding affinity to CETP, ready access and unlimited supply, 1CL8 and 1CL10 are expected to prove powerful tools for studies on the role of CETP in atherogenesis.

assayHDL biologyobesity

Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 19 August 2026. Methods.