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      超實(shí)用干貨—用嘌呤霉素篩個(gè)穩(wěn)轉(zhuǎn)細(xì)胞株

      嘌呤霉素(Puromycin)是一種由白黑鏈霉菌產(chǎn)生的氨基苷類抗生素,是氨酰-tRNA分子3´末端的類似物,能夠與核糖體的A位點(diǎn)結(jié)合并摻入到延伸的肽鏈中,打亂核糖體上的肽轉(zhuǎn)運(yùn),造成翻譯過(guò)程中不成熟鏈終止,從而抑制蛋白質(zhì)合成。

      31.png

      圖1嘌呤霉素結(jié)構(gòu)式(CAS NO. 53-79-2)
       

      嘌呤霉素產(chǎn)生菌Streptomyces alboniger內(nèi)發(fā)現(xiàn)的pac基因編碼嘌呤霉素N-乙酰轉(zhuǎn)移酶(pac),賦予機(jī)體對(duì)嘌呤霉素產(chǎn)生抗性。這一特性如今普遍應(yīng)用于篩選特定攜帶pac基因質(zhì)粒的哺乳動(dòng)物穩(wěn)定轉(zhuǎn)染細(xì)胞株。嘌呤霉素在細(xì)胞穩(wěn)轉(zhuǎn)株篩選中的普遍應(yīng)用與慢病毒載體的特性有關(guān),現(xiàn)在商業(yè)化的慢病毒載體多數(shù)都攜帶pac基因。在某些特定情況下,嘌呤霉素亦可以用來(lái)篩選轉(zhuǎn)化攜帶pac基因質(zhì)粒的大腸桿菌菌株。嘌呤霉素作用迅速,在低濃度下即可快速導(dǎo)致細(xì)胞死亡。貼壁哺乳細(xì)胞對(duì)濃度為2-5 µg/ml的嘌呤霉素較為敏感,而懸浮細(xì)胞對(duì)濃度低至0.5-2 µg/mL的嘌呤霉素已經(jīng)很敏感。對(duì)嘌呤霉素穩(wěn)定耐藥的哺乳細(xì)胞可在一周內(nèi)生成。
       

      穩(wěn)轉(zhuǎn)細(xì)胞株篩選

      實(shí)驗(yàn)原理:

      通過(guò)將外源DNA/shRNA克隆到帶有pac基因的載體上,重組載體轉(zhuǎn)染至宿主細(xì)胞并整合到其染色體中,并隨細(xì)胞分裂穩(wěn)定傳遞,最后用嘌呤霉素進(jìn)行篩選。

      準(zhǔn)備及預(yù)實(shí)驗(yàn):

      1. 建議使用濃度

      哺乳動(dòng)物細(xì)胞:1-10 μg/mL,最佳濃度需要預(yù)實(shí)驗(yàn)來(lái)確定。

      大腸桿菌:LB瓊脂培養(yǎng)基篩選穩(wěn)定轉(zhuǎn)化pac基因的大腸桿菌,使用濃度為125 μg/mL。使用嘌呤霉素篩選大腸桿菌穩(wěn)轉(zhuǎn)株需要精確的pH值調(diào)節(jié)。

      2. 溶解方法

      用蒸餾水溶解嘌呤霉素配制成50 mg/mL的母液,0.22 μm濾膜過(guò)濾除菌后分裝,于-20℃凍存。

      3. 嘌呤霉素殺滅曲線的確定(以shRNA轉(zhuǎn)染或者慢病毒轉(zhuǎn)導(dǎo)為例)

      嘌呤霉素有效篩選濃度跟細(xì)胞類型、生長(zhǎng)狀態(tài)、細(xì)胞密度、細(xì)胞代謝情況及細(xì)胞所處細(xì)胞周期位置等有關(guān),確定殺死未轉(zhuǎn)染細(xì)胞的最低濃度嘌呤霉素至關(guān)重要。初次做實(shí)驗(yàn)一定要先進(jìn)行Puromycin梯度篩選預(yù)實(shí)驗(yàn),建立殺死曲線(kill curve)。

      1)以5~8×104 cells/孔的密度24孔板鋪板,培養(yǎng)過(guò)夜。

      2)準(zhǔn)備篩選培養(yǎng)基:含不同濃度嘌呤霉素的新鮮培養(yǎng)基(如0-15 μg/mL,至少5個(gè)梯度)。

      3)更換新鮮配制的篩選培養(yǎng)基,繼續(xù)培養(yǎng),并觀察細(xì)胞生長(zhǎng)情況,每2-3天更換新鮮篩選培養(yǎng)基。

      4)每日觀察細(xì)胞存活情況,4-6天內(nèi)有效殺死所有非轉(zhuǎn)染細(xì)胞的藥物為最低濃度。

      穩(wěn)轉(zhuǎn)株的篩選

      慢病毒感染48-72h后(70-80%融合度),將細(xì)胞培養(yǎng)于含適當(dāng)濃度Puromycin的培養(yǎng)液中,篩選至少48h。當(dāng)對(duì)照未轉(zhuǎn)染的細(xì)胞加puro組全部死亡時(shí),感染病毒組剩下全部是陽(yáng)性細(xì)胞。

      【注】:①當(dāng)細(xì)胞處于分裂活躍期時(shí),抗生素作用最明顯。細(xì)胞過(guò)于密集,抗生素產(chǎn)生的效力會(huì)明顯下降。細(xì)胞密度最好不超過(guò)25%。②每日觀察細(xì)胞生長(zhǎng)狀態(tài),嘌呤霉素的篩選至少需要48 h,有效濃度嘌呤霉素的篩選周期一般在3-10天。③病毒的MOI越高,每個(gè)細(xì)胞含有的shRNA拷貝和嘌呤霉素耐性基因越多。在做嘌呤霉素篩選時(shí),越高M(jìn)OI,含越多pac拷貝的細(xì)胞能耐受更高的嘌呤霉素濃度,調(diào)整嘌呤霉素的濃度去篩選轉(zhuǎn)染細(xì)胞,但是嘌呤霉素的濃度不能低于殺死曲線的最低有效濃度;

      2)加入含有最低濃度的Puromycin培養(yǎng)基擴(kuò)增細(xì)胞,待qPCR檢測(cè)結(jié)果合格后進(jìn)行凍存。

      翌圣生物推出兩種狀態(tài)的嘌呤霉素產(chǎn)品助力穩(wěn)轉(zhuǎn)細(xì)胞株篩選!
       

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      客戶使用該產(chǎn)品發(fā)表的科研文獻(xiàn)(不完全統(tǒng)計(jì):部分)

      累計(jì)影響因子已達(dá)300!

      [1] Zhang D, Liu Y, Zhu Y, et al. A non-canonical cGAS-STING-PERK pathway facilitates the translational program critical for senescence and organ fibrosis. Nat Cell Biol. 2022;24(5):766-782. doi:10.1038/s41556-022-00894-z(IF:28.824)

      [2] Lu T, Zhang Z, Zhang J, et al. CD73 in small extracellular vesicles derived from HNSCC defines tumour-associated immunosuppression mediated by macrophages in the microenvironment. J Extracell Vesicles. 2022;11(5):e12218. doi:10.1002/jev2.12218(IF:25.841)

      [3] Meng F, Yu Z, Zhang D, et al. Induced phase separation of mutant NF2 imprisons the cGAS-STING machinery to abrogate antitumor immunity. Mol Cell. 2021;81(20):4147-4164.e7. doi:10.1016/j.molcel.2021.07.040(IF:17.970)

      [4] Chen S, Liu S, Wang J, et al. TBK1-Mediated DRP1 Targeting Confers Nucleic Acid Sensing to Reprogram Mitochondrial Dynamics and Physiology. Mol Cell. 2020;80(5):810-827.e7. doi:10.1016/j.molcel.2020.10.018(IF:15.584)

      [5] Zhao Q, Zheng K, Ma C, et al. PTPS Facilitates Compartmentalized LTBP1 S-Nitrosylation and Promotes Tumor Growth under Hypoxia. Mol Cell. 2020;77(1):95-107.e5. doi:10.1016/j.molcel.2019.09.018(IF:14.548)

      [6] Mo J, Liu F, Sun X, et al. Inhibition of the FACT Complex Targets Aberrant Hedgehog Signaling and Overcomes Resistance to Smoothened Antagonists. Cancer Res. 2021;81(11):3105-3120. doi:10.1158/0008-5472.CAN-20-3186(IF:12.701)

      [7] Zou Y, Wang A, Shi M, et al. Analysis of redox landscapes and dynamics in living cells and in vivo using genetically encoded fluorescent sensors. Nat Protoc. 2018;13(10):2362-2386. doi:10.1038/s41596-018-0042-5(IF:12.423)

      [8] Mao L, Chen J, Lu X, et al. Proteomic analysis of lung cancer cells reveals a critical role of BCAT1 in cancer cell metastasis. Theranostics. 2021;11(19):9705-9720. Published 2021 Sep 27. doi:10.7150/thno.61731(IF:11.556)

      [9] Han L, Zhang F, Liu Y, et al. Uterus globulin associated protein 1 (UGRP1) binds podoplanin (PDPN) to promote a novel inflammation pathway during Streptococcus pneumoniae infection. Clin Transl Med. 2022;12(6):e850. doi:10.1002/ctm2.850(IF:11.492)

      [10] Zhang M, Liu F, Zhou P, et al. The MTOR signaling pathway regulates macrophage differentiation from mouse myeloid progenitors by inhibiting autophagy. Autophagy. 2019;15(7):1150-1162. doi:10.1080/15548627.2019.1578040(IF:11.059)

      [11] Zhang S, Yang Z, Bao W, et al. SNX10 (sorting nexin 10) inhibits colorectal cancer initiation and progression by controlling autophagic degradation of SRC. Autophagy. 2020;16(4):735-749. doi:10.1080/15548627.2019.1632122(IF:11.059)

      [12] Zhang Y, Ding H, Wang X, et al. MK2 promotes Tfcp2l1 degradation via β-TrCP ubiquitin ligase to regulate mouse embryonic stem cell self-renewal. Cell Rep. 2021;37(5):109949. doi:10.1016/j.celrep.2021.109949(IF:9.423)

      [13] Jiang Y, Dong Y, Luo Y, et al. AMPK-mediated phosphorylation on 53BP1 promotes c-NHEJ. Cell Rep. 2021;34(7):108713. doi:10.1016/j.celrep.2021.108713(IF:9.423)

      [14] Sun Q, Ye Y, Gui A, et al. MORTALIN-Ca2+ axis drives innate rituximab resistance in diffuse large B-cell lymphoma. Cancer Lett. 2022;537:215678. doi:10.1016/j.canlet.2022.215678(IF:8.679)

      [15] Jin R, Zhao A, Han S, et al. The interaction of S100A16 and GRP78 actives endoplasmic reticulum stress-mediated through the IRE1α/XBP1 pathway in renal tubulointerstitial fibrosis. Cell Death Dis. 2021;12(10):942. Published 2021 Oct 13. doi:10.1038/s41419-021-04249-8(IF:8.469)

      [16] Zhang P, Zhang Z, Fu Y, et al. K63-linked ubiquitination of DYRK1A by TRAF2 alleviates Sprouty 2-mediated degradation of EGFR. Cell Death Dis. 2021;12(6):608. Published 2021 Jun 11. doi:10.1038/s41419-021-03887-2(IF:8.469)

      [17] Zhao T, Li Y, Shen K, Wang Q, Zhang J. Knockdown of OLR1 weakens glycolytic metabolism to repress colon cancer cell proliferation and chemoresistance by downregulating SULT2B1 via c-MYC. Cell Death Dis. 2021;13(1):4. Published 2021 Dec 17. doi:10.1038/s41419-021-04174-w(IF:8.469)

      [18] Zhou R, Wu Q, Wang M, et al. The protein phosphatase PPM1A dephosphorylates and activates YAP to govern mammalian intestinal and liver regeneration. PLoS Biol. 2021;19(2):e3001122. Published 2021 Feb 25. doi:10.1371/journal.pbio.3001122(IF:8.029)

       

       


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