A general strategy for generating intact, full-length IgG antibodies that penetrate into the cytosol of living cells

Dong Ki Choi, Jeomil Bae, Seung Min Shin, Ju Yeon Shin, Sunghoon Kim, Yong Sung Kim

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49 Citations (Scopus)


Full-length IgG antibodies cannot cross cell membranes of living cells; this limits their use for direct targeting of cytosolic proteins. Here, we describe a general strategy for the generation of intact, full-length IgG antibodies, herein called cytotransmabs, which internalize into living cells and localize in the cytosol. We first generated a humanized light chain variable domain (VL) that could penetrate into the cytosol of living cells and was engineered for association with various subtypes of human heavy chain variable domains (VHs). When light chains with humanized VL were coexpressed with 3 heavy chains (HCs), including 2 HCs of the clinically approved adalimumab (Humira®) and bevacizumab (Avastin®), all 3 purified IgG antibodies were internalized into the cytoplasm of living cells. Cytotransmabs primarily internalized into living cells by the clathrin-mediated endocytic pathway through interactions with heparin sulfate proteoglycan that was expressed on the cell surface. The cytotransmabs escaped into the cytosol from early endosomes without being further transported into other cellular compartments, like the lysosomes, endoplasmic reticulum, Golgi apparatus, and nucleus. Furthermore, we generated a cytotransmab that co-localized with the targeted cytosolic protein when it was incubated with living cells, demonstrating that the cytotransmab can directly target cytosolic proteins. Internalized cytotransmabs did not show any noticeable cytotoxicity and remained in the cytosol for more than 6 h before being degraded by proteosomes. These results suggest that cytotransmabs, which efficiently enter living cells and reach the cytosolic space, will find widespread uses as research, diagnostic, and therapeutic agents.

Original languageEnglish
Pages (from-to)1402-1414
Number of pages13
Issue number6
Publication statusPublished - 2014 Nov 1

Bibliographical note

Funding Information:
This work was supported by the Pioneer Research Center Program (2014M3C1A3051470), the Global Frontier Project (2013M3A6A4043874), and the Priority Research Center Program (2012–0006687) through the National Research Foundation of Korea, by the Ministry of Science, ICT & Future Planning.

Publisher Copyright:
© 2014 Taylor & Francis Group, LLC.

All Science Journal Classification (ASJC) codes

  • Immunology and Allergy
  • Immunology


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