N-Terminus pQE Vector Set

N-말단 His-tagged 단백질의 고수준 발현을 위해 사용


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N-Terminus pQE Vector Set

Cat. No. / ID:  32915

각각 25µg: pQE-9, pQE-30, pQE-31, pQE-32, pQE-40
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N-Terminus pQE Vector Set은/는 분자생물학 분야에 사용하기 위한 것입니다. 이 제품은 질병의 진단, 예방, 또는 치료용이 아닙니다.

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  • 빠른 클로닝을 위해 세 개의 판독 프레임 모두에 MCS가 포함된 pQE-30 벡터
  • 잘 발현되지 않는 단백질을 위한 pQE-40 벡터, 짧은 펩티드
  • pQE-40 벡터는 DHFR 융합을 발현하여 안정성과 항원성을 향상시킵니다

Product Details

이 세트는 N-말단 His-tagged 단백질의 발현을 위한 5가지 벡터(pQE-9, pQE-30, pQE-31, pQE-32, pQE-40)를 제공합니다. pQE-30, pQE-31, pQE-32는 3개의 판독 프레임 모두에서 다중 클로닝 부위(Multiple Cloning Site, MCS)를 제공하는 반면 pQE-9는 대체로 더 짧은 다중 클로닝 부위를 가지고 있습니다. pQE-40은 DHFR 융합 단백질의 발현을 위해 설계되었으며, DHFR이 안정성과 항원성을 모두 향상시키기 때문에 발현이 잘 안 되는 단백질이나 단백질 분해되기 쉬운 짧은 펩티드의 발현에 권장됩니다. DHFR 자체는 마우스와 래트(rat)에서 면역원성이 거의 나타나지 않기 때문에 DHFR 융합 단백질은 에피토프 스크리닝에 이상적입니다.


QIAexpress pQE 벡터에 존재하는 구성 요소
구성 요소 설명
최적화된 promoter/operator 구성 요소 파지 T5 promoter와 두 개의 lac operator 염기서열로 구성되며, 이는 lac repressor의 결합 가능성을 높이고 강력한 T5 promoter의 효율적인 억제를 보장합니다
합성 리보솜 결합 부위 RBSII 효율적인 번역을 위해 사용
6xHis-tag 코딩 염기서열 5' 또는 3'에서 polylinker 클로닝 영역까지
번역 중지 코돈 모든 판독 프레임에서 발현 구조체를 편리하게 준비할 수 있습니다
두 가지 강력한 전사 종결 인자 파지 람다의 t0, E. coli rrnB 오페론의 T1을 사용하여 연속 판독 전사를 방지하고 발현 구조의 안정성을 보장합니다
ColE1 복제 기점 pBR322 유래
베타 락타마제 유전자(bla) 암피실린 내성 부여





관심 단백질을 코딩하는 삽입물을 적절한 구조체로 복제하고(자세한 정보는 QIAexpressionist 안내서 참조) 발현에 적합한 E. coli 균주로 변형합니다. IPTG를 추가하면 발현이 유도됩니다. 벡터 pQE-TriSystem 구조체는 E. coli로 형질 전환하거나, 곤충 세포에서 재조합 단백질 발현을 위한 셔틀 벡터로 사용하거나, 포유류 세포에 감염시킬 수 있습니다.


QIAexpress Expression System은 다음을 포함한
많은 애플리케이션에 적합한 고수준 단백질 발현을 제공합니다.

  • 기능적, 형태적으로 활성화된 단백질의 정제
  • 항체 생산을 위한 변성 조건에서의 정제
  • 3차원 구조 결정을 위한 결정화
  • 단백질–단백질 및 단백질–DNA 상호작용 관련 분석

Supporting data and figures


Tag6xHis tag
N- or C-terminal tagN-말단 태그
Expression speciesE. coli
Tag removal sequence아니요
In-frame cloning necessary
All three reading frames provided


Safety Data Sheets (1)
Selection Guides (1)
Kit Handbooks (1)
A handbook for high-level expression and purification of 6xHis-tagged proteins
Vector Sequences & Maps (2)
For the pQE-40 vector
For the pQE 9 vector
Certificates of Analysis (1)


Modulating RssB activity: IraP, a novel regulator of sigma(S) stability in Escherichia coli.
Bougdour A; Wickner S; Gottesman S;
Genes Dev; 2006; 20 (7):884-97 2006 Apr 1 PMID:16600914
Characterization of the putative alpha subunit of a heterotrimeric G protein in rice.
Iwasaki Y; Kato T; Kaidoh T; Ishikawa A; Asahi T;
Plant Mol Biol; 1997; 34 (4):563-72 1997 Jul PMID:9247538


How can I express toxic protein in E. coli?

To reduce the effects of protein toxicity on bacterial cell growth prior to induction, the level of basal transcription that occurs in the absence of induction (“leakiness”) should be repressed as much as possible, and the number of generations before induction should be kept to a minimum.

For very toxic proteins, we recommend using the pQE-80L series of expression vectors in the M15[pREP4] E. coli host strain. The pQE-80L vectors have a cis-lacIq gene that overexpresses the lac repressor, in addition to a lacI repressor gene present in trans on a separate pREP4 plasmid. This combination of two repressor modules results in highly efficient suppression of recombinant protein expression prior to induction and gives the best chance of successful expression of toxic proteins. Furthermore, induction of the toxic protein should be done at a time point as late as possible, and the IPTG concentration used for induction should be reduced. Conditions have to be optimized for each application.

Another alternative is to use cell-free protein biosynthesis systems , like the EasyXpress Protein Synthesis Kit. The advantages of cell-free expression systems include time savings, the possibility to produce proteins that are toxic and the ability to adapt reaction conditions to the requirements of the synthesized protein.


FAQ ID -373
Why is the pQE DNA provided in QIAexpress Kits blue in color?
The blue color results from bromophenol blue added to the plasmid DNA prior to lyophilization to make the DNA more easily visible. After the DNA pellet is resuspended in water or Tris-HCl, the dye will not inhibit downstream applications such as transformation of bacterial cells or restriction enzyme digestion.
FAQ ID -487
What is the size, charge and isoelectric point of the DHFR protein in the pQE vectors?

The native Dihydrofolate Reductase (DHFR) protein has the following technical features:

  • Molecular Weight: 21.5 kDa
  • Isoelectric Point: 8.5
  • Charge at pH 7.0: 2.2

DHFR expressed in QIAexpress vectors pQE-16 and pOE-40 has the following technical features:


  • Molecular Weight: 23.1 kDa
  • Isoelectric Point: 9.1
  • Charge at pH 7.0: 5.2


  • Molecular Weight: 24.5 kDa
  • Isoelectric Point: 9.2
  • Charge at pH 7.0: 7.2
FAQ ID -470
How can I increase expression of my 6xHis-tagged protein in E. coli?

Low-level expression can occur because the protein is toxic or unstable, or because the expression construct is not maintained in the cells during growth. In some cases, the 5' end of the inserted DNA sequence may encode elements that interfere with transcription or translation (e.g., masking of the Shine-Dalgarno sequence by stem-loop structures resulting from inverted repeats). In these instances, the sequence being expressed should be checked and modified if necessary. Modifications of growth media and different host strains may also have an effect on expression.

Please review the section "Specific considerations" in the Chapter 'Expression in E. coli' of the QIAexpressionist Handbook and refer to standard literature in protein science (e.g., Current Protocols in Protein Science, eds. John Wiley and Sons, New York) for additional information.

FAQ ID -63
If pQE40 is used to express a fusion protein with DHFR, can the DHFR be cleaved afterwards?
No, since there is no cleavage site included in pQE40 to remove the DHFR.
FAQ ID -513
Which primers can I use for sequencing pQE-expression vector constructs?
All pQE vectors (except pQE-TriSystem) can be sequenced using any of the primers described on page 118 of the QIAexpressionist.
FAQ ID -343
Is dihydrofolate reductase (DHFR) immunogenic?

Murine DHFR, used as a fusion protein to enable expression of very small proteins and peptides with the QIAexpress System, is poorly immunogenic in mouse and rats. It may however lead to an immune response in rabbits and goat. DHFR protein is encoded in the QIAexpress vectors pQE-16 or pQE-40.

FAQ ID -471
How can I increase the amount of soluble recombinant protein in E. coli expression?

The QIAexpress Protein Purification System allows easy solubilization of 6xHis-tagged proteins sequestered into insoluble inclusion bodies by using denaturants such as 6 M Guanidine-HCl or 8 M Urea, or a variety of detergents. Proteins purified under denaturing conditions can then be refolded if necessary before use (please see: Wingfield, P. T., Palmer, I., and Liang, S.-M. (1995). Folding and purification of insoluble (inclusion-body) proteins from Escherichia coli. In: Current Protocols in Protein Science, vol. 1, Coligan, J. E., Dunn, B. M., Ploegh, H. L., Speicher, D. W., and Wingfield, P.T. eds. Wiley and Sons, Inc. New York, pp. 6.5.1–6.5.27.). The QIAexpressionist also contains recommendations for refolding proteins prior to the Appendix section of the handbook.

To increase levels of soluble protein, here are a few recommendations:

  • a reduction in growth temperature following induction may be helpful. Growth temperature often directly affects both expression levels and protein solubility, and lower temperatures will reduce expression levels leading to a higher amount of soluble protein.
  • the culture can be grown to a higher cell density before induction and the expression period can be kept to a minimum.
  • The IPTG concentration can be reduced from 1 mM to 0.005 mM, which would reduce the expression level by 90–95%.
  • it may be sufficient to change the host strain used, since certain strains tolerate some proteins better than others and allow higher levels of expression before forming inclusion bodies.
  • many proteins require metal cofactors in order to remain soluble, and the addition of metal salts to the culture media may be helpful. If the metal requirements of the protein are not known, a number of different supplements should be tested. Note that some divalent cations may interfere with protein binding to Ni-NTA.



FAQ ID -64
What is the origin of replication and the plasmid copy number of the pQE vectors?
The QIAexpress pQE vectors contain a pBR322 derived ColE1 origin of replication and are classified as low-copy plasmids (by our estimate, approximately 20-30 copies per cell; exact numbers have not been determined). The pQE-TriSystem Vector has a pUC origin of replication and is classified as a high-copy vector. Please see also FAQ 350 for general information on replication origins and copy numbers of various commonly used plasmids.
FAQ ID -338
How should I propagate pQE expression plasmids?

QIAexpress pQE vectors and constructs can be maintained in any E. coli strain that is ampicillin-sensitive and carries the pREP4 repressor plasmid, or harbors the lacIq gene on the F-factor episome.

M15 and SG13009 E. coli host strains carry lacI on the plasmid pREP4, while XL1-Blue or the JM series contain an episomal copy of lacIq.

LacIq is a mutation of lacI that produces very high levels of the lac repressor. Initial cloning and propagation using XL1-Blue is recommended because plasmid preparations derived from QIAexpress host strains will also contain pREP4 DNA, which could make clone analysis more difficult.

Alternatively, the pQE-80L series of expression vectors which encodes a lacIq repression module, allows use of any E. coli host strain.

FAQ ID -58
Do pQE vectors contain the CAT gene?
The chloramphenicol acetyl transferase gene (CAT) present between t0 and T1 has no promoter and is not normally expressed. Depending on the bacterial strain and insert,low CAT activities may be detectable
FAQ ID -362
How can I be sure that I am harvesting my induced bacterial culture at the best time point for protein expression?

To optimize the expression of a given recombinant protein, a time-course analysis of the level of protein expression in the induced culture is recommended. Intracellular protein content is often a balance between the amount of soluble protein in the cells, the formation of inclusion bodies, and protein degradation. By checking the 6xHis-tagged protein present at various times after induction in the soluble and insoluble fractions, the optimal induction period can be established, and the bacterial culture can be harvested at this time. It may be useful to perform plasmid Mini preparations on culture samples during the time-course to enable monitoring of plasmid (expression construct) maintenance.

Below, you can see an example of a time course of recombinant protein expression using the QIAexpress System. You can find this information also in the Section 'Expression in E. coli' in the QIAexpressionist Handbook. The handbook is an important resource for useful background information and protocols. For instructions on how to isolate protein from the soluble and insoluble fractions of induced cultures please see Protocol 14. "Protein minipreps of 6x His-tagged proteins from E. coli under native conditions" and Protocol 19. "6xHis-tagged protein minipreps under denaturing conditions."




Time course of expression using the QIAexpress System. Expression of 6xHis-tagged DHFR was induced with 1 mM IPTG. Aliquots were removed at the times indicated and purified on Ni-NTA Agarose under denaturing conditions. Proteins were visualized by Coomassie staining. Yields per liter culture were 2.8, 5.5,12.3, 33.8, and 53.9 mg, respectively. ■A Crude cell lysate; ■B purification with Ni-NTA. 1: flow-through, 2 & 3: first and second eluates; M: markers; C: noninduced control.



FAQ ID -788