S. cerevisiae VN-fusion Library Set (5,809 strains)

본 제품은 이분자 형광 상보 (bimolecular fluorescence complementation) 기법을 적용하여 효모 세포에서 단백질 상호작용을 유전체적 (genome-wide) 수준에서 분석하기 위한 효모 균주 라이브러리 제품입니다. 이분자 형광 상보 기법은 형광단백질을 N-말단 및 C-말단 절편으로 나눈 후 상호작용을 알아보고자 하는 두 단백질에 부착하여 발현되게 한 다음, 두 단백질이 상호작용을 하기 위해 가까워질 경우 형광단백질의 두 절편이 합쳐져 온전한 형광단백질이 형성될 때 나타나는 형광을 분석하는 방법입니다. 그리하여 살아있는 세포를 대상으로 단백질 상호작용의 동적 분석에 적용할 수 있는 방법 중 가장 장점이 많고 성공 가능성이 높은 것으로 받아들여지고 있습니다. S. cerevisiae VN-Fusion Set 제품은 기존의 세포 외 (in vitro) 분석 혹은 인위적인 단백질 발현을 통한 단백질 상호작용 분석 방법과 달리, 세포 내 (in vivo)에서 자신의 고유한 프로모터로부터 자연 상태로 발현되는 단백질들 간에 일어나는 상호작용을 효모의 전체 단백질을 대상으로 신속하게 분석할 수 있습니다. 또한 yeast proteome의 약 93% 확보하여 5,809개의 VN-tagged Open Reading Frames (ORFs) 으로 구성되어 있어 단백질의 상호작용을 유전체적 수준에서 분석 가능합니다.

카탈로그 번호

The yeast Saccharomyces cerevisiae (S. cerevisiae) is a recognized simple eukaryote model system which genome can be easily manipulated. The S. cerevisiae VN-Fusion Library was created by Dr. Won-Ki Huh of Seoul National University (Korea).
The VN-Fusion Library consists of 5,809 VN-tagged Open Reading Frames (ORFs) covering 93% of the yeast proteome.

Bimolecular Fluorescence Complementation (BiFC) assay

Most biological processes are carried out and regulated by dynamic networks of protein-protein interactions. The Bimolecular Fluorescence Complementation (BiFC) assay is now regarded as one of the most advanced and powerful tools for studying in vivo detection of protein–protein interactions in several orgarnisms. The BiFC assay is based on the formation of a fluorescent complex by fragments of yellow fluorescent protein, brought together by association of two interacting partners fused to the fragments. This approach enables visualization of the subcellular localizations of specific protein complexes in the normal intracellular environment.

Shyu et al, 2008

Features and Benefits

 A powerful tool for studying protein-protein interactions in living cells
   - Non-invasive method for analyzing fluorescence without the need for any external cofactors

 Clear visualization of subcellular protein-protein interaction localization
   - Formation of a fluorescent complex

 Stronger signal and direct readout measurable with relatively simple equipment
   - Using a fluorescence microscope

 Genome-wide high-throughput screening possible
   - 93% yeast proteome coverage

 Unknown protein function analysis through functional complementation is possible

 Analysis of proteinylation (ubiquitination, sumoylation, neddylation) is possible


S. cerevisiae VN-Fusion Library
Strains 5,809 strains
Selection Marker KIURA3
Genotype All S. cerevisiae VN-Fusion strains were derived from BY4741
(MATa his3Δ1 leu2Δ0 met15Δ0 ura3Δ0)
Culture media YPD: for general culture and maintenance medium
SC-Ura or SC-His: for medium selection & counter selection (auxotrophic culture)
Strain verification Medium selection & Counter selection
Check PCR
Storage Store at -70°C (Glycerol type)
Store at 22°C to 25°C (Agar type)
References Monitoring G protein-coupled receptor activation using an adenovirus-based β-arrestin bimolecular fluorescence complementation assay
Yong Bhum Song, Chul O. Park, Jae-Yeon Jeong, Won-Ki Huh Anal Biochem. 2014. 15(449), 32-41.
• More information

Genome-wide bimolecular fluorescence complementation analysis of SUMO interactome in yeast
Min-Kyung Sung, Gyubum Lim, Dae-Gwan Yi, Yeon Ji Chang, Eun Bin Yang, KiYoung Lee, and
Won-Ki Huh Genome Res. 2013. 23(4), 736-746.
• More information

Nsi1 plays a significant role in the silencing of ribosomal DNA in Saccharomyces cerevisiae
Cheol Woong Ha, Min-Kyung Sung, Won-Ki Huh Nucleic Acids Res. 2012. 40(11), 4892-4903
• More information

Interactomic study on interaction between lipid droplets and mitochondria
Jing Pu, Cheol Woong Ha, Shuyan Zhang, Jong Pil Jung, Won-Ki Huh, Pingsheng Liu Protein Cell. 2011. 2(6), 487-496.
• More information

in vivo quantification of protein-protein interactions in Saccharomyces cerevisiae using bimolecular fluorescence complementation assay
Min-Kyung Sung, Won-Ki Huh J Microbiol Methods. 2010. 83(2), 194-201.
• More information

A vector system for efficient and economical switching of C-terminal epitope tags in Saccharomyces cerevisiae
Min-Kyung Sung, Cheol Woong Ha, Won-Ki Huh Yeast. 2008. 25(4), 301-311.
• More information

Bimolecular fluorescence complementation analysis system for in vivo detection of protein-protein interaction in Saccharomyces cerevisiae
Min-Kyung Sung, Won-Ki Huh Yeast. 2007. 24(9), 767-775.
• More information

Construction, verification and experimental use of two epitope-tagged collections of budding yeast strains
Russell Howson, Won-Ki Huh, Sina Ghaemmaghami, James V. Falvo, Kiowa Bower, Archana Belle, Noah Dephoure, Dennis D. Wykoff, Jonathan S. Weissman and Erin K. O’Shea
Comp Funct Genom. 2005. 6, 2–16.
• More information

Global analysis of protein localization in budding yeast
Won-Ki Huh, James V. Falvo, Luke C. Gerke, Adam S. Carroll, Russell W. Howson, Jonathan S. Weissman and Erin K. O’Shea Nature. 2003. 425, 686-691.
• More information
Patent 10-2009-0048746


A ~2.5 kb DNA cassette including the VN and KlURA3 marker gene was amplified by PCR using pFA6a-VN-KlURA3 as a template, and "universal" F2CORE (5'-GGTCGACGGATCCCCGGGTT-3') and R1CORE (5'-TCGATGAATTCGAGCTCGTT-3') primers. The resulting DNA cassette was transformed into ~6,000 yeast strains from the TAP-tagged collection (Ghaemmaghami et al., 2003). The transformed cells were spread on SC-Ura plates and incubated at 30°C for 3 days. Among several colonies, 10 colonies were picked and streaked on fresh SC-Ura plates, and incubated at 30°C for 24 hours. To check correct switching to the VN tag, cells grown on SC-Ura plates were replica-plated onto SC-His plates. Cells growing on SC-His plates were discarded.

Construction of a VN-tagged strain from the TAP-tagged strain


To confirm that the TAP tag was successfully switched to the VN tag, the colonies selected by SC-Ura medium were checked by colony PCR using the CHK1 [gene-specific primer] and CHK2 [5'-CACCATGGTGGCGATGGATC-3'] primers. A small aliquot of freshly grown cells was resuspended in 5 μl water and boiled in a 96-well plate (99°C for 5 min in the thermal cycler). 5 μl boiled cells and 2.5 μl of 5 μM unique CHK1 primer were added to a PCR premix (AccuPower® HotStart PCR PreMix [Bioneer, K-5050, Korea], 0.25 μl 50 μM CHK2 primer) and PCR was performed [94°C 3 min, 35×(94°C 30 s, 50°C 30 s, 72°C 1 min), 72°C 10 min]. We analyzed the results of PCR by agarose gel electrophoresis, identifying correct integrants by the presence of a PCR product of appropriate size [~600 bp].

PCR validation


Visualization of subcellular location of protein–protein interaction

Example: Fluorescence images of diploid cells expressing the C-terminally VN-tagged Sis1 and the C-terminally VC-tagged Sis1 together.

Sis1 is a Type II HSP40 co-chaperone that interacts with the HSP70 protein Ssa1 (Luke et al., 1991), and has been shown to form a homodimer (Sha et al., 2000). The bimolecular fluorescence complementation (BiFC) signal was clearly detected in the nucleus and the cytoplasm, indicating that the VN-tagged Sis1 interacted with the VC-tagged Sis1 in the nucleus and the cytoplasm, where Sis1 is reported to be localized (Huh et al., 2003). The BiFC signal was not detected in the diploid cells expressing either the VN-tagged Sis1 or the VC-tagged Sis1 alone.



S. cerevisiae VN-Fusion Library-Manual


S. cerevisiae VN-Fusion Library-MSDS


S. cerevisiae VN-Fusion Library - 2011 Brochure

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Cat. No. Product Description Price Add to Cart
S. cerevisiae VN-Fusion Individual Strains
V-1010VN-A S. cerevisiae VN-Fusion Individual Strains, Agar type $200.00 Search & Order
V-1010VN-G S. cerevisiae VN-Fusion Individual Strains, Glycerol type $200.00 Search & Order
S. cerevisiae VN-Fusion Library Set
V-1030VN S. cerevisiae VN-Fusion Library Set, Glycerol type
: 5,809 strains, 63 plates (96-well)
$20,000.00 List & Order
Related Item A : Validation Primer
V-1030VN-P AccuOligo® S. cerevisiae VN-Fusion Library
Validation Primer Set : 63 plates (96-well)
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Related Item B : Yeast protein tagging vectors for BiFC analysis
V-1010-V1 pFA6a-VN173-HIS3MX6 (5ug) $30.00 (handling charge) E-mail Us
V-1010-V2 pFA6a-VC155-HIS3MX6 (5ug) $30.00 (handling charge) E-mail Us
V-1010-V3 pFA6a-VN173-TRP1 (5ug) $30.00 (handling charge) E-mail Us
V-1010-V4 pFA6a-VC155-TRP1 (5ug) $30.00 (handling charge) E-mail Us
V-1010-V5 pFA6a-VN173-KanMX6 (5ug) $30.00 (handling charge) E-mail Us
V-1010-V6 pFA6a-VC155-KanMX6 (5ug) $30.00 (handling charge) E-mail Us
V-1010-V7 pFA6a-HIS3MX6-PGAL1-VN173 (5ug) $30.00 (handling charge) E-mail Us
V-1010-V8 pFA6a-HIS3MX6-PGAL1-VC155 (5ug) $30.00 (handling charge) E-mail Us
V-1010-V9 pFA6a-TRP1-PGAL1-VN173 (5ug) $30.00 (handling charge) E-mail Us
V-1010-V10 pFA6a-TRP1-PGAL1-VC155 (5ug) $30.00 (handling charge) E-mail Us
V-1010-V11 pFA6a-KanMX6-PGAL1-VN173 (5ug) $30.00 (handling charge) E-mail Us
V-1010-V12 pFA6a-KanMX6-PGAL1-VC155 (5ug) $30.00 (handling charge) E-mail Us
V-1010-V13 pFA6a-HIS3MX6-PCET1-VN173 (5ug) $30.00 (handling charge) E-mail Us
V-1010-V14 pFA6a-HIS3MX6-PCET1-VC155 (5ug) $30.00 (handling charge) E-mail Us
V-1010-V15 pFA6a-TRP1-PCET1-VN173 (5ug) $30.00 (handling charge) E-mail Us
V-1010-V16 pFA6a-TRP1-PCET1-VC155 (5ug) $30.00 (handling charge) E-mail Us
V-1010-V17 pFA6a-KanMX6-PCET1-VN173 (5ug) $30.00 (handling charge) E-mail Us
V-1010-V18 pFA6a-KanMX6-PCET1-VC155 (5ug) $30.00 (handling charge) E-mail Us
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