Bispecific and human disease-related anti-keratin rabbit monoclonal antibodies

Guo Zhong Tao, Ikuo Nakamichi, Nam On Ku, Jing Wang, Maria Frolkis, Xiaosong Gong, Weimin Zhu, Robert Pytela, M. Bishr Omary

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15 Citations (Scopus)

Abstract

Rabbit antibodies may have favorable properties compared to mouse antibodies, including high affinities and better antigen recognition. We used a biochemical and reverse immunologic approach to generate and characterize rabbit anti-phospho-keratin and anti-keratin monoclonal antibodies (MAb). Human keratins 8 and 18 (K8/K18) were used as immunogens after isolation from cells pretreated with okadaic acid or pervanadate to promote Ser/Thr or Tyr hyperphosphorylation, respectively. Selected rabbit MAb were tested by immunofluorescence staining, immunoprecipitation, and 2-dimensional gels. Keratin phospho and non-phospho-mutants were used for detailed characterization of two unique antibodies. One antibody recognizes a K8 G61-containing epitope, an important epitope given that K8 G61C is a frequent mutation in human liver diseases. This antibody binds K8 that is not phosphorylated on S73, but its binding is ablated by G61 but not S73 mutation. The second antibody is bispecific in that it simultaneously recognizes two epitopes: one phospho (K8 pS431) conformation-independent and one non-phospho conformation-dependent, with both epitopes residing in the K8 tail domain. Therefore, a reverse immunologic and biochemical approach is a viable tool for generating versatile rabbit MAb for a variety of cell biologic applications including the potential identification of physiologic phosphorylation sites.

Original languageEnglish
Pages (from-to)411-422
Number of pages12
JournalExperimental Cell Research
Volume312
Issue number4
DOIs
Publication statusPublished - 2006 Feb 15

Bibliographical note

Funding Information:
This work is supported by NIH DK47918 and Department of Veterans Affairs Merit Awards (M.B.O.) and NIH Digestive Disease Center grant DK56339 Cell Imaging Core. G.-Z.T. is supported in part by a Crohn's and Colitis Foundation of America Research Award. We are grateful to Dr. Sheri M. Krams for assisting with the liver explant harvesting, Evelyn Resurreccion for tissue sectioning and immunofluorescence staining and to Liying Xie for assisting with subcloning.

All Science Journal Classification (ASJC) codes

  • Cell Biology

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