Skip to main content

A novel anti-p21Ras scFv antibody reacting specifically with human tumour cell lines and primary tumour tissues



The ras genes play an important role in the development and progression of human tumours. Neutralizing Ras proteins in the cytoplasm could be an effective approach to blocking ras signalling. In this study, we prepared anti-p21Ras single chain fragment variable antibody (scFv) and investigated its immunoreactivity with human tumours.


The coding sequences of H-ras, K-ras, and N-ras were separately ligated into the vector pET-28a(+). Then, recombinant expressing plasmids were induced by IPTG for p21Ras expression in E. coli. Hybridoma cell lines producing anti-p21Ras monoclonal antibodies were isolated using wildtype p21Ras proteins as immunogens. Anti-p21Ras scFv antibody was prepared from the hybridoma by the phage scFv display method. The immunoreactivity of the anti-p21Ras monoclonal antibody and the scFv antibody was identified by ELISA and immunocytochemistry.


We prokaryotically expressed wildtype H-p21Ras, K-p21Ras and N-p21Ras and generated the hybridoma cell line KGH-R1, producing anti-p21Ras monoclonal antibodies. It was demonstrated that KGH-R1 monoclonal antibody could recognize wildtype and mutated H-p21Ras, K-p21Ras and N-p21Ras in human tumour cell lines.

In all 14 types of primary human cancer tissues tested, the monoclonal antibody presented strong immunoreactivity but showed weak or negative immunoreactivity in the corresponding normal tissues. Subsequently, we prepared anti-p21Ras scFv from hybridoma KGH-R1, which showed the same immunoreactivity as the original monoclonal antibody. Sequence analysis demonstrated that the nucleotides and amino acids of the scFv exhibited an approximately 50 % difference from the anti-p21Ras scFv reported previously.


This study presents a novel anti-p21Ras scFv antibody. Our data suggest that the scFv may be useful for ras signalling blockage and may be a potential therapeutic antibody for ras-derived tumours.

Peer Review reports


Because of the important role of ras in carcinogenesis and progression, the ras signalling pathway has attracted considerable attention as a target for anticancer therapy. The ras gene product, p21Ras, is a monomeric membrane-localized G protein of 21 kD, which functions as a molecular switch converting signals from the cell membrane to the nucleus and linking receptor and nonreceptor tyrosine kinase activation to downstream cytoplasmic or nuclear events. The biological effects of p21Ras depend on its biochemical properties of being a small GTP-binding protein and on its correct cellular location at the cytoplasmic face of the plasma membrane [1]. Thus, the neutralization of p21Ras proteins in the cytoplasm using specific antibodies may block ras signalling and constitute a promising therapeutic strategy [2].

It is well known that whole antibodies can penetrate cells only with difficulty due to their large molecular size. In recent years, a series of low-molecular-weight antibodies containing antigen-binding domains have been explored to develop antibody-based drugs with better tumour penetration, such as antigen-binding fragment [3], single chain fragment variable (scFv) [4], and single-domain antibodies [5]. It has been found that scFv antibodies penetrate the cell membrane better than whole antibodies [6, 7] and result in no immunological rejections due to lacking the Fc fragment [8, 9], giving them advantages as intracellular immunization and therapeutic antibodies. Currently, scFv antibodies have been applied in many fields, including anti-viral and cancer therapy [1012].

Both overexpression and mutation can activate ras genes. The overexpression of p21Ras has been detected in many human tumours [1317]. The overexpression of ras family members led to the acquired resistance of cancer to cetuximab treatment [18]. It has been found that ras mutations are present in approximately 33 % of all human tumours [19]. K-ras mutations occur frequently in non-small-cell lung, colorectal, and pancreatic carcinomas; H-ras mutations are common in bladder, kidney, and thyroid carcinomas; and N-ras mutations are found in melanoma, hepatocellular carcinoma, and haematologic malignancies [20]. However, previously reported anti-p21Ras antibodies were derived from mutated p21Ras antigen [2123]. In this study, we isolated hybridoma cell lines producing anti-p21Ras monoclonal antibodies, using wildtype p21Ras proteins as immunogens, prepared anti-p21Ras scFv antibodies from the hybridomas, and then investigated their immunoreactivity with human tumour cell lines and primary tumour tissues.


Preparation of the wildtype p21Ras proteins

The coding sequences (CDS) of the H-ras, K-ras, and N-ras genes were chemically synthetized according to their wildtype mRNA sequences published in NCBI GenBank: NM_005343 for H-ras, M54968 for K-ras, and BC005219 for N-ras. The restriction enzyme Bam HI cutting site GGATCC was ligated at the 5′ end of the CDS, and the Hind III cutting site AAGCTT was ligated at the 3′ end during synthesis. After digestion with Bam HI and Hind III, the three CDS fragments were ligated separately into the vector pET-28a(+) by T4 ligase. Then, recombinant expressing plasmids were transformed into E. coli BL21(DE3) and screened by kanamycin, induced by IPTG for p21Ras expression [24]. Expressed p21Ras proteins were purified by Ni2+-NTA resin with the mild denaturant urea and then underwent SDS-PAGE analysis, followed by dialysis for renaturation.

Preparation of hybridomas producing broad-spectrum anti-p21 Ras mAb

Balb/c mice were immunized by injection with wildtype H-p21Ras expressed prokaryotically. The mouse splenic B lymphocytes were fused with myeloma cell lines SP2/0. After selective culture using HAT selective culture medium, the fused hybridoma cells were screened by an indirect ELISA method with all three wildtype p21Ras proteins and then cloned and subcloned to obtain hybridoma cell lines producing monoclonal antibodies against wildtype H-p21Ras, K-p21Ras and N-p21Ras. All hybridoma cell lines were subcloned twice. Finally, the hybridoma cell lines were injected into the peritoneal cavity of Balb/c mice to produce monoclonal antibodies [21]. A completed ARRIVE guidelines checklist is included in Additional file 1. Human cancer cell lines were used to identify the immunoreactivity of the monoclonal antibodies by Western blot. Primary tumour tissues and their corresponding normal tissues were employed to investigate the tumour reactivities of the monoclonal antibodies by immunohistochemical staining, and the results were described by HSCOREs [25].

Construction of scFv phage display library

Hybridoma cell line KGH-R1, which produced excellent broad-spectrum anti-p21Ras mAb, was used to construct a phage scFv display library. Total RNA was isolated from KGH-R1 cells using RNAiso plus (MrcGene) and reverse transcribed to cDNA using the RevertAid™ H Minus First Strand cDNA Synthesis Kit (Fermentas). The heavy chain variable region (VH) and light chain variable region (VL) were amplified using primers provided by the Recombinant Phage Antibody System (GE Healthcare, RPAS). A DNA linker complementary to the 3′ end of VH and 5′ end of VL was ligated between the VH and VL fragments by overlapping extended PCR amplification to construct the scFv gene.

The phage scFv display library was constructed according to the RPAS system manual (GE Healthcare). Briefly, the scFv fragment genes and the phagemid pCANTAB-5E were sequentially digested with the Sfi I and Not I restriction enzymes. After purification by agarose gel extraction, both the scFvs fragments and the pCANTAB-5E vector with Sfi I and Not were ligated using T4 DNA ligase, transformed into competent E. coli TG1 cells, and cultured on SOBAG plates (SOB-AG, containing 100 μg/ml ampicillin and 2 % glucose) at 37 °C. All of the bacterial single colonies that grew on the SOBAG plate were collected, mixed and cultured in 2 × YTAG medium. The helper phage M13K07 at 1011 pfu was added to the collections and co-cultured at 30 °C for 1 h to obtain recombinant phages expressing the scFv antibodies and g3p fusion proteins on the surface. The scFv phages were purified and concentrated by polyethylene glycol (20 % PEG8000, 2.5 mol/L NaCl). The pellet was resuspended in PBS to obtain the phage scFv display library.

Enrichment of scFv phage

The phage scFv display library underwent three rounds of panning using H-p21Ras, K-p21Ras and N-p21Ras protein antigens, respectively. Briefly, the flask was coated with p21Ras protein dissolved in 0.1 mM NaHCO3. After blocking with BSA, the library was added to the flask and incubated at 37 °C for 2 h, followed by washing with PBST (containing 0.05 % tween-20, pH 7.4) 10 times, followed by washing PBS (without Tween-20) an additional 10 times to remove unbound phage particles. Specifically bound phages were eluted with 0.1 M HCL/glycine (containing 0.1 % BSA, pH 2.2). The eluent was neutralized with pH 9.0 Tris/HCl, was used to infect TG1 cells and was then rescued with helper phage M13K07. These enriched scFv phages were used in the next round of panning [26, 27]. In each panning round, the numbers of input and output phages were counted using the double agar layer method.

Identification of scFv-phages

E. coli TG1 cells were infected by the final enriched phage pools and cultured on an SOB-AG plate. Single colonies were picked and rescued individually with M13K07 in 96-well plates. The phages from individual wells were assayed by ELISA to detect their specific antigen binding activities, utilizing p21Ras proteins as antigens, scFv-phage as primary antibody, and HRP-conjugated mouse anti-M13 mAb as second antibody. The positive phages were further identified by Sfi I and Not I enzyme digestion and PCR amplification with pCANTAB-5E primers (forward, S1: 5-CAACGTGAAAAAATTATTATTCGC-3; reverse, S6: 5-GTAAATGAATTTTC TGTATGAGG-3). The amplified products were ligated into a pMD18-T vector for sequence analysis.

Bioinformatics analysis of scFv gene and 3D modelling

The sequence of the scFv gene was blasted with known murine genes for homology analysis in the GenBank database, as described previously [28]. The amino acid residues, CDRs and FRs were determined according to the IMGT numbering system and Kabat by IgBLAST [28]. The 3D structure of scFv antibody was generated by SWISS-MODEL [29, 30].

Expression of soluble scFv antibodies

The expression of soluble scFv antibodies was performed according to the manual and reference [31]. Briefly, the p21Ras-positve phages were used to infect HB2151 cells and cultured in plates. A single colony was picked and grown overnight to express soluble anti-p21Ras scFv antibodies with E-tag peptide at the end through the induction of IPTG. The soluble scFv antibodies were extracted from the HB2151 culture and concentrated by PEG8000/NaCl.

Immunocytochemistry/immunohistochemistry and Western blot

Human tumour cell lines harbouring wildtype or mutated Ras [32, 33], primary tumour tissues and the corresponding normal tissues were employed to detect the immunoreactivities of the scFv antibodies by immunohistochemical staining. The soluble scFv antibodies were used as the primary antibody, whereas Anti-E-tag monoclonal antibody conjugated with HRP served as the second antibody to bind E-tag protein ligated to the end of the scFv antibody. The scFv immunoreactivity with p21Ras was further detected by Western blot in the tumour cell lines MDA-MB-435, MDA-MB-231 and SKOV3 (ATCC USA) and the normal cell line KMB17 (normal human embryonic diploid lung fibroblast cell, constructed by the Institute of Medical Biology, Chinese Academy of Medical Sciences). β-actin was used as a control, with anti-β-actin monoclonal antibody conjugated with HRP.

Ethics statement

This study including animal work has the approval of the Ethics Board of Kunming General Hospital and is also in accordance with the Helsinki Declaration of 1975. Written informed consent was obtained from every patient. All human tissues were processed anonymously.


Preparation of hybridomas and anti-p21Ras monoclonal antibodies

By cloning the CDS of the H-ras, K-ras, N-ras genes into pET-28(+) vectors, we constructed a prokaryotically expressive vector (Fig. 1a, b) that effectively expressed H-p21Ras, K-p21Ras and N-p21Ras protein in E. coli BL21. SDS-PAGE analysis showed that the apparent molecular weight of the three p21Ras proteins was 25 KD (Fig. 1c). The purity of p21Ras protein was more than 95 %.

Fig. 1
figure 1

Wildtype p21Ras proteins and anti-p21Ras monoclonal antibodies. a The plasmid map of recombinant pET-28a(+) vector expressing H-ras, in which H-ras gene CDS with Bam HI and Hind III restriction enzyme sites was cloned into a pET-28a(+) vector with a histidine tag-compatible end. b The three recombinant pET28a(+) plasmids were digested into two fragments by Bam HI and Hind III, the 570 bp of the ras gene CDS and 5340 bp of the pET-28a(+) vector. c SDS–PAGE analysis showed that the molecular weight of the three p21Ras proteins with His tag was 25 kDa. d KGH-R1 monoclonal antibody against three p21Ras proteins demonstrated strong immunoreactivity to cancer tissues but negative immunoreactivity to corresponding normal tissues

H-p21Ras was used as an immunogen to immunize BALB/c mice to isolate hybridomas. To achieve monoclonal antibodies that simultaneously recognized H-p21Ras, K-p21Ras and N-p21Ras, the three p21Ras were used as antigens to screen the hybridomas in an ELISA assay. In total, we obtained 13 hybridomas that produced monoclonal antibodies against the three different p21Ras proteins. Karyotype analysis showed that the median chromosome numbers of the 13 hybridomas were 97–100. Immunochromatography indicated that the monoclonal antibodies produced by all 13 hybridomas were of the IgG2b/κ subtype. Monoclonal antibodies in ascites reached a high titre of 1:128000. The immunoreactivities of the monoclonal antibody KGH-R1 were determined by Western blot and immunohistochemistry. The KGH-R1 monoclonal antibody demonstrated positive immunoreactivities in all 13 human solid tumour cell lines and 2/6 leukaemia cell lines (Table 1). In all 14 types of primary human cancer tissues tested here, the monoclonal antibody presented strong immunoreactivity but showed weak or negative immunoreactivity in the corresponding normal tissues (Table 2, Fig. 1d).

Table 1 Immunoreactivity of KGH-R1 mAb in human tumour cell lines
Table 2 Immunoreactivity of KGH-R1 mAb in human tumours and corresponding normal tissues

Construction and panning of scFv phage display library

The scFv gene consists of a heavy chain variable region (VH) and a light chain variable region (VL), joined by a neutral linker (Fig. 2a). We amplified VH (340 bp) and VL (320 bp) from the cDNA of the KGH-R1 hybridoma. Then, we connected both to DNA linker by overlapping extended PCR to construct a 750 bp scFv gene (Fig. 2b). The scFv gene repertoire was ligated to the phagemid pCANTAB 5E and then transformed into competent TG1 cells and grown in SOBAG plates, obtaining 1 × 107 TG1 colonies transformed by the recombinant phage plasmids (Fig. 2c). We collected all of the TG1 colonies, co-cultured them with M13KO7 helper phages, and established the scFv phage display library, in which scFv-g3p fusion proteins were expressed at the tips of the phages. To obtain phages expressing anti-p21Ras scFv antibodies from the library, the library was selected and panned using the H-p21Ras, K-p21Ras, and N-p21Ras proteins, in turn. After three rounds of panning, the eluted phages were maintained at 1 × 106 pFU/mL, and the number of input phage pools was maintained at 1 × 109 pFU/mL (Fig. 2d).

Fig. 2
figure 2

Preparation of anti p21Ras scFv. a Schematic diagram of scFv. The variable region of the heavy chain (VH) and the variable region of the light chain (VL) were combined with a polypeptide linker. b Construction of scFv gene. The 340 bp VH fragment and 325 bp VL fragment were amplified from the cDNA of the KGH-R1 hybridoma. This assembly reaction ultimately produces 750 bp of scFv. c The recombinant pCANTAB5E-scFv plasmid was digested into two fragments by Sfi I and Not I: 750 bp of scFv and 4472 bp of pCANTAB-5E vector. d The phage-ELISA showed that after three rounds of panning by H-p21Ras, K-p21Ras and N-p21Ras antigens, in turn, the number of output phages (unbound phages) was constant at 1 × 106 PFU/ml, whereas the number of input phage was constant at 1 × 109 PFU/ml

Characteristics of anti-p21Ras scFv antibodies

To obtain monoclonal phages expressing anti-p21Ras scFv antibodies, we infected TG1 cells with the enriched scFv phage pool and plated them on SOBAG plates. Then, 40 colonies were rescued by M13K07. Indirect ELISA tests showed that all 40 colonies expressed scFv antibodies that could bind H-p21Ras, K-p21Ras and N-p21Ras simultaneously. Recombinant phagemids were isolated from each of the 40 colonies and digested by Sfi I and Not I and then ligated with pMD18-T vector for DNA sequencing. Sequence analysis demonstrated that the sequences of the 40 colonies were the same. The number of amino acids and complementary determining regions (CDRs) of the VH and VL domains were determined using IgBLAST. KGHR1-scFv had 738 nucleotides encoding 246 amino acids, of which VH consisted of 117 amino acids, VL consisted of 114 amino acids, and the flexible amino acid linker consisted of 15 amino acids. Both the VH and VL fragments had 3 CDR regions and 4 FR regions (Fig 3a). Homology analysis revealed that VH belongs to murine subfamily III and that VL belongs to the subfamily VII κ chains. We constructed a three-dimensional model of the scFv antibody by the SWISS MODEL method. In the 3D model, scFv consists of the VH chain and the VL chain connected by a polypeptide linker chain (Fig. 3b).

Fig. 3
figure 3

Bioinformatics and immunoreactivity of the anti-p21Ras scFv. a Amino acid sequence of anti-p21Ras scFv with appropriate regions for framework and CDR residues, differing from the previously reported Y13-159 scFv and Y13-238 scFv. b 3D model of anti-p21Ras scFv generated by bioinformatics. Variable heavy chain (VH) and light chain (VL) regions of the antibody were connected by a single 15-amino acid linker (L, green). c Western blot detected anti-p21Ras scFv antibody-specific binding with p21Ras protein in the cells, where strong immunoreactivity was found in p21Ras-overexpressing tumour cell lines; however, weak immunoreactivity was observed in the normal cell line KMB17 with low p21Ras expression. d Immunohistochemistry revealed that anti-p21Ras scFv antibody exhibited strongly positive staining in human tumour cell lines and primary solid tumour tissues

Immunoreactivity of soluble anti-p21Ras scFv antibodies

Soluble anti-p21Ras scFv antibodies were prepared by infecting the non-amber suppressor E. coli strain HB2151 with the recombinant phages. The Western blot assay showed that anti-p21Ras scFv antibody could specifically bind the p21Ras protein in the tested cells (Fig. 3c). We further evaluated the immunoreactivities of scFv in human tumour cell lines, primary solid tumour tissues and normal tissues by immunohistochemical staining. The results demonstrated that the soluble scFv displayed strong immunostaining in all the human tumour cell lines and all types of primary human cancer tissues tested here. However, all of the corresponding normal tissues showed negative immunostaining. The granular positive signal was mainly located in the cytoplasm and membrane (Table 3, Fig. 3d). The results indicated that the obtained scFv could recognize the p21Ras antigen epitope in tumour cells.

Table 3 Immunoreactivity of KGHR1-scFv antibody in human tumour tissues and cell lines


Antibody-based drugs are promising agents for cancer therapy. In recent years, certain antibody drugs have been clinically approved and used frequently in cancer treatment. Trastuzumab, a chimeric monoclonal antibody against Her2 protein, is the most impressive target drug for breast cancer therapy [34, 35]. Rituximab, an anti-CD20 monoclonal antibody, is another of the most effective drugs in B cell malignant lymphoma treatment [36]. The gene ras is a well-known and important oncogene involved in the development and progression of many human tumours, but no antibody drugs targeting the ras gene have been applied clinically. The main reason is that the intracellular location of p21Ras has limited the effects of antibodies because intact antibodies can not penetrate the cell membrane. Thus, small molecular antibodies, such as scFv, are proposed to treat ras-derived tumours.

Because hybridoma cell lines are the most important resources for scFv [3739], we established anti-p21Ras hybridomas using prokaryotically expressed wildtype H-p21Ras protein as an immunogen. H-p21Ras, K-p21Ras and N-p21Ras were used to screen the hybridoma clones. Finally, the hybridoma KGH-R1, producing a broad-spectrum monoclonal antibody against the three p21Ras proteins, was isolated. Interestingly, the monoclonal antibodies reacted with both wildtype and mutated p21Ras in human tumour cell lines and presented excellent immunoreactivities with the majority of human tumour cell lines and primary tumour tissues but negative immunostaining in the corresponding normal tissues. The characteristics mentioned above give these antibodies important value as therapeutic prodrugs. To our knowledge, this study is the first to use wildtype p21 Ras as an immunogen to prepare monoclonal antibodies. The anti-p21Ras monoclonal antibodies reported previously were derived from mutated p21Ras, of which Y13-259 and Y13-238 were generated using p21 protein encoded by the v-ras gene of the Harvey murine sarcoma virus as an immunogen [22]. RAP-1 ~ 5 were generated utilizing a synthetic H-p21Ras peptide reflecting amino acid positions 10–17 with a mutation at codon 12 as the immunogen [23]. RASK1 ~ 16 were generated using mutated K-p21Ras from Kirsten murine sarcoma virus as the immunogen [21].

Antibody genes can be fused into phage genes, and then the antibodies can be expressed and displayed on the surface of the phages as fusion proteins [40]. The phage display library has thus become the most popular technique for constructing and selecting scFv antibodies from hybridomas or B lymphocytes due to its benefits, such as the high diversity of the antigenic repertoire and the ability to rapidly select specific antibodies [41]. In this study, we employed the phage display library method to isolate scFv antibodies against human p21Ras proteins. Fortunately, we obtained scFv antibodies that maintained all of the immunoreactivities of the original monoclonal KGH-R1 antibodies, including the recognition of wildtype and mutated p21Ras proteins, reaction with H-p21Ras, K-p21Ras and N-p21Ras, and strong immunostaining in tumour cell lines and primary tumours. These results showed that scFv is useful for ras signalling blockage and may be a therapeutic antibody for ras-derived tumours.

The scFv antibodies presented here were dramatically different from previous anti-p21Ras scFv in both their nucleotide sequences and their amino acid sequences [42, 43]. There was a 49.8 % difference from Y13-259 scFv and a 53.73 % difference from Y13-238 scFv, mostly located in the CDRs (Fig. 3a). Our data indicated that KGH-R1 scFv recognizes different antigen epitopes, based on a comparison of Y13-259 scFv and Y13-238 scFv, and it is a novel anti-p21Ras scFv antibody.


In conclusion, this study presents a novel anti-p21Ras scFv antibody, KGH-R1 scFv, produced by hybridoma and phage scFv display library methods. Sequence analysis showed that KGH-R1 scFv antibody has an approximately 50 % difference from reported anti-p21Ras scFv antibodies. The KGH-R1 scFv antibody could recognize wildtype and mutated H-p21Ras, K-p21Ras, and N-p21Ras and exhibited strong immunoreactivity with human tumour cell lines and primary tumours. It is suggested that the scFv may be useful for ras signalling blockage and as a therapeutic antibody for ras-derived tumours.



Single chain fragment variable




Guanosine triphosphate


Coding sequences


National Center for Biotechnology Information


Isopropyl β-D-1-thiogalactopyranoside


Sodium dodecyl sulfate-polyacrylamide gel electrophoresis


Monoclonal antibody


Hypoxanthine, aminopterin, thymidine


Enzyme-linked immunosorbent assay


Heavy chain variable region


Light chain variable region


Phosphate buffered saline


PBS containing 0.05 % tween-20


Albumin from bovine serum


Horseradish peroxidase


Complementarity-determining region


Framework region


Human epidermal growth factor receptor 2


  1. Lener M, Horn IR, Cardinale A, Messina S, Nielsen UB, Rybak SM, Hoogenboom HR, Cattaneo A, Biocca S. Diverting a protein from its cellular location by intracellular antibodies. The case of p21Ras. Eur J Biochem. 2000;267(4):1196–205.

    Article  CAS  PubMed  Google Scholar 

  2. Adjei AA. Blocking oncogenic Ras signaling for cancer therapy. J Natl Cancer Inst. 2001;93(14):1062–74.

    Article  CAS  PubMed  Google Scholar 

  3. Xin C, Ye S, Ming Y, Shenghua Z, Qingfang M, Hongxing G, Xu S, Yuanfu X, Yuan Z, Dongmei F, et al. Efficient inhibition of B-cell lymphoma xenografts with a novel recombinant fusion protein: anti-CD20Fab-LDM. Gene Ther. 2010;17(10):1234–43.

    Article  CAS  PubMed  Google Scholar 

  4. Sheng W, Shang Y, Miao Q, Li Y, Zhen Y. Antitumor efficacy of the scFv-based fusion protein and its enediyne-energized analogue directed against epidermal growth factor receptor. Anticancer Drugs. 2012;23(4):406–16.

    Article  CAS  PubMed  Google Scholar 

  5. Miao QF, Liu XY, Shang BY, Ouyang ZG, Zhen YS. An enediyne-energized single-domain antibody-containing fusion protein shows potent antitumor activity. Anticancer Drugs. 2007;18(2):127–37.

    Article  CAS  PubMed  Google Scholar 

  6. Bird RE, Hardman KD, Jacobson JW, Johnson S, Kaufman BM, Lee SM, Lee T, Pope SH, Riordan GS, Whitlow M. Single-chain antigen-binding proteins. Science. 1988;242(4877):423–6.

    Article  CAS  PubMed  Google Scholar 

  7. Yokota T, Milenic DE, Whitlow M, Schlom J. Rapid tumor penetration of a single-chain Fv and comparison with other immunoglobulin forms. Cancer Res. 1992;52(12):3402–8.

    CAS  PubMed  Google Scholar 

  8. Demarest SJ, Glaser SM. Antibody therapeutics, antibody engineering, and the merits of protein stability. Curr Opin Drug Discov Devel. 2008;11(5):675–87.

    CAS  PubMed  Google Scholar 

  9. Schirrmann T, Al-Halabi L, Dubel S, Hust M. Production systems for recombinant antibodies. Front Biosci. 2008;13:4576–94.

    Article  CAS  PubMed  Google Scholar 

  10. Novinger LJ, Ashikaga T, Krag DN. Identification of tumor-binding scFv derived from clonally related B cells in tumor and lymph node of a patient with breast cancer. Cancer Immunol Immunother. 2015;64(1):29–39.

    Article  CAS  PubMed  Google Scholar 

  11. Buhler P, Wetterauer D, Gierschner D, Wetterauer U, Beile UE, Wolf P. Influence of structural variations on biological activity of anti-PSMA scFv and immunotoxins targeting prostate cancer. Anticancer Res. 2010;30(9):3373–9.

    PubMed  Google Scholar 

  12. Yao YD, Sun TM, Huang SY, Dou S, Lin L, Chen JN, Ruan JB, Mao CQ, Yu FY, Zeng MS, et al. Targeted delivery of PLK1-siRNA by ScFv suppresses Her2+ breast cancer growth and metastasis. Sci Transl Med. 2012;4(130):130–48.

    Article  Google Scholar 

  13. Gallick GE, Kurzrock R, Kloetzer WS, Arlinghaus RB, Gutterman JU. Expression of p21ras in fresh primary and metastatic human colorectal tumors. Proc Natl Acad Sci U S A. 1985;82(6):1795–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Gerosa MA, Talarico D, Fognani C, Raimondi E, Colombatti M, Tridente G, De Carli L, Della Valle G. Overexpression of N-ras oncogene and epidermal growth factor receptor gene in human glioblastomas. J Natl Cancer Inst. 1989;81(1):63–7.

    Article  CAS  PubMed  Google Scholar 

  15. Hamdy S, Aprikian A, Begin L, Fair W, Bazinet M. Ras p21 overexpression is a late event in prostate-cancer. Int J Oncol. 1994;4(3):627–31.

    CAS  PubMed  Google Scholar 

  16. Novara R, Coda R, Martone T, Vineis P. Exposure to aromatic amines and ras and c-erbB-2 overexpression in bladder cancer. J Occup Environ Med. 1996;38(4):390–3.

    Article  CAS  PubMed  Google Scholar 

  17. Murugan AK, Munirajan AK, Tsuchida N. Ras oncogenes in oral cancer: the past 20 years. Oral Oncol. 2012;48(5):383–92.

    Article  CAS  PubMed  Google Scholar 

  18. Saki M, Toulany M, Rodemann HP. Acquired resistance to cetuximab is associated with the overexpression of Ras family members and the loss of radiosensitization in head and neck cancer cells. Radiother Oncol. 2013;108(3):473–8.

    Article  CAS  PubMed  Google Scholar 

  19. Schmukler E, Kloog Y, Pinkas-Kramarski R. Ras and autophagy in cancer development and therapy. Oncotarget. 2014;5(3):577–86.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Pylayeva-Gupta Y, Grabocka E, Bar-Sagi D. RAS oncogenes: weaving a tumorigenic web. Nat Rev Cancer. 2011;11(11):761–74.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Yoshida K, Hamatani K, Koide H, Ikeda H, Nakamura N, Akiyama M, Tsuchiyama H, Nakayama E, Shiku H. Preparation of anti-ras Mr 21,000 protein monoclonal antibodies and immunohistochemical analyses on expression of ras genes in human stomach and thyroid cancers. Cancer Res. 1988;48(19):5503–9.

    CAS  PubMed  Google Scholar 

  22. Furth ME, Davis LJ, Fleurdelys B, Scolnick EM. Monoclonal antibodies to the p21 products of the transforming gene of Harvey murine sarcoma virus and of the cellular ras gene family. J Virol. 1982;43(1):294–304.

    CAS  PubMed  PubMed Central  Google Scholar 

  23. Hand PH, Thor A, Wunderlich D, Muraro R, Caruso A, Schlom J. Monoclonal antibodies of predefined specificity detect activated ras gene expression in human mammary and colon carcinomas. Proc Natl Acad Sci U S A. 1984;81(16):5227–31.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Zhou Y, Zhang J, Jin H, Chen Z, Wu Q, Li W, Yue M, Luo C, Wang M. Prokaryotic expression and refolding of EGFR extracellular domain and generation of phage display human scFv against EGFR. Biomed Pharmacother. 2013;67(8):737–43.

    Article  CAS  PubMed  Google Scholar 

  25. Huang CL, Yokomise H, Kobayashi S, Fukushima M, Hitomi S, Wada H. Intratumoral expression of thymidylate synthase and dihydropyrimidine dehydrogenase in non-small cell lung cancer patients treated with 5-FU-based chemotherapy. Int J Oncol. 2000;17(1):47–54.

    CAS  PubMed  Google Scholar 

  26. Liu Y, Chang J, Chen Y, Wan B, Wang Y, Zhang G. Construction of a human scFv antibody library with VH regions randomized and its application. Biotechnol Lett. 2012;34(7):1203–8.

    Article  CAS  PubMed  Google Scholar 

  27. Chang C, Takayanagi A, Yoshida T, Shimizu N. Screening of scFv-displaying phages recognizing distinct extracellular domains of EGF receptor by target-guided proximity labeling method. J Immunol Methods. 2011;372(1–2):127–36.

    Article  CAS  PubMed  Google Scholar 

  28. Wang R, Huang A, Liu L, Xiang S, Li X, Ling S, Wang L, Lu T, Wang S. Construction of a single chain variable fragment antibody (scFv) against tetrodotoxin (TTX) and its interaction with TTX. Toxicon. 2014;83:22–34.

    Article  CAS  PubMed  Google Scholar 

  29. Babaei A, Zarkesh-Esfahani SH, Gharagozloo M. Production of a recombinant anti-human CD4 single-chain variable-fragment antibody using phage display technology and its expression in Escherichia coli. J Microbiol Biotechnol. 2011;21(5):529–35.

    Article  CAS  PubMed  Google Scholar 

  30. Schwede T, Kopp J, Guex N, Peitsch MC. SWISS-MODEL: An automated protein homology-modeling server. Nucleic Acids Res. 2003;31(13):3381–5.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Wong C, Waibel R, Sheets M, Mach JP, Finnern R. Human scFv antibody fragments specific for the epithelial tumour marker MUC-1, selected by phage display on living cells. Cancer Immunol Immunother. 2001;50(2):93–101.

    Article  CAS  PubMed  Google Scholar 

  32. Bos JL. The ras gene family and human carcinogenesis. Mutat Res. 1988;195(3):255–71.

    Article  CAS  PubMed  Google Scholar 

  33. Cochet O, Kenigsberg M, Delumeau I, Virone-Oddos A, Multon MC, Fridman WH, Schweighoffer F, Teillaud JL, Tocque B. Intracellular expression of an antibody fragment-neutralizing p21 ras promotes tumor regression. Cancer Res. 1998;58(6):1170–6.

    CAS  PubMed  Google Scholar 

  34. Bayoudh L, Afrit M, Daldoul O, Zarrad M, Boussen H. [Trastuzumab (herceptin) for the medical treatment of breast cancer]. Tunis Med. 2012;90(1):6–12.

    PubMed  Google Scholar 

  35. Servitja S, Ramos M, Gil M, Sanchez-Rovira P, Vazquez-Estevez S, Virizuela JA, Garcia-Estevez L, Velasco A, Tusquets I. Multicenter, phase II, nonrandomized study of docetaxel plus trastuzumab every 21 days as the primary therapy in metastatic breast cancer overexpressing HER2. Anticancer Drugs. 2012;23(2):239–46.

    Article  CAS  PubMed  Google Scholar 

  36. Oflazoglu E, Audoly LP. Evolution of anti-CD20 monoclonal antibody therapeutics in oncology. MAbs. 2010;2(1):14–9.

    Article  PubMed  PubMed Central  Google Scholar 

  37. Liu A, Ye Y, Chen W, Wang X, Chen F. Expression of VH-linker-V L orientation-dependent single-chain Fv antibody fragment derived from hybridoma 2E6 against aflatoxin B1 in Escherichia coli. J Ind Microbiol Biotechnol. 2015;42(2):255–62.

    Article  PubMed  Google Scholar 

  38. Chen W, Hu L, Liu A, Li J, Chen F, Wang X. Expression and characterization of single-chain variable fragment antibody against staphylococcal enterotoxin A in Escherichia coli. Can J Microbiol. 2014;60(11):737–43.

    Article  CAS  PubMed  Google Scholar 

  39. Zhu Q, Guo D, Feng L, Sun D. Expression and Purification of the scFv from hybridoma cells secreting a monoclonal antibody against S PROTEIN of PEDV. Monoclon Antib Immunodiagn Immunother. 2013;32(1):41–6.

    CAS  PubMed  PubMed Central  Google Scholar 

  40. Clackson T, Hoogenboom HR, Griffiths AD, Winter G. Making antibody fragments using phage display libraries. Nature. 1991;352(6336):624–8.

    Article  CAS  PubMed  Google Scholar 

  41. Chan CE, Chan AH, Lim AP, Hanson BJ. Comparison of the efficiency of antibody selection from semi-synthetic scFv and non-immune Fab phage display libraries against protein targets for rapid development of diagnostic immunoassays. J Immunol Methods. 2011;373(1–2):79–88.

    Article  CAS  PubMed  Google Scholar 

  42. Cochet O, Kenigsberg M, Delumeau I, Duchesne M, Schweighoffer F, Tocque B, Teillaud JL. Intracellular expression and functional properties of an anti-p21Ras scFv derived from a rat hybridoma containing specific lambda and irrelevant kappa light chains. Mol Immunol. 1998;35(17):1097–110.

    Article  CAS  PubMed  Google Scholar 

  43. Werge TM, Biocca S, Cattaneo A. Intracellular immunization. Cloning and intracellular expression of a monoclonal antibody to the p21ras protein. FEBS Lett. 1990;274(1–2):193–8.

    CAS  PubMed  Google Scholar 

Download references


This work was supported by the grants from the National Natural Science Foundation of China (No 30872994 and No 81460464) and the Scientific and Technological key project of Yunnan Province (No 2006SG11).

Author information

Authors and Affiliations


Corresponding author

Correspondence to Ju-Lun Yang.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

JLY contributed to the conception and design of the study. DXL, SJZ, YGZ, DJZ, LYY and HBC were involved in the acquisition of the data. All authors participated in the analysis and interpretation of the data. QF drafted the manuscript. JLY contributed to the revision of the manuscript. JLY contributed to the supervision of the study. All authors read and approved the final manuscript.

Additional files

Additional file 1:

The ARRIVE Guidelines Checklist. (DOC 694 kb)

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Yang, JL., Liu, DX., Zhen, SJ. et al. A novel anti-p21Ras scFv antibody reacting specifically with human tumour cell lines and primary tumour tissues. BMC Cancer 16, 131 (2016).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: