Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

The inside scoop—evaluating gene delivery methods

Techniques for delivering nucleic acids into mammalian cells have been around for decades. But tools and reagents continue to improve and target a broader range of cells and applications. Laura Bonetta reports.

HeLa cells transduced with a self-inactivating retrovirus from Clontech's pQX (retroQ) series, which expresses green fluorescent protein. (Courtesy of Clontech.)

Pick a paper, any paper. Chances are that somewhere in the Methods section there is a description of a step for introducing DNA or RNA in cells. Although it has become a routine procedure, in vitro gene delivery can still be a challenge, especially when working with frail or scarce mammalian cells.

The mammalian cell membrane is impenetrable to large molecules that, like DNA, carry an electrical charge. Researchers have thus come up with an arsenal of tricks—from using carrier molecules and viral vectors to pocking holes in the membrane—to sneak nucleic acids through. But no one method can be applied to all types of cells or experiments. “You look at the articles that have been published and find one that has done some comparison of different transfection methods for your cells. But if you don't have any clues, you have to try different reagents, to find what will work best in your hands,” says Nina Iversen, a researcher at the University of Oslo. The good news is that there is no shortage of reagents to try!

Solution revolution

A popular way to get DNA and RNA inside cells is to use carrier molecules. Such methods do not require expensive equipment and, from a technical standpoint, are less difficult to use than viruses. They rely on the fact that nucleic acids can interact with positively charged molecules, such as cationic lipids and polymers, to form complexes that are more palatable to the cell.

Carrier molecules on the market today owe their existence to the discovery, almost four decades ago, that coating DNA with DEAE-dextran would allow it to get past the cell membrane1—a process dubbed 'transfection'. In the early 1970s, researchers discovered that they could also transfect DNA using calcium phosphate, a less toxic chemical2. Some labs still use these reagents, which can be purchased as stand-alones or in kits. For example, Promega's ProFection mammalian transfection systems offer optimized buffers and solutions for either calcium phosphate– or DEAE-dextran–mediated transfection. But for many researchers, the newer, lipid-based reagents offer greater ease of use and efficiency with lower toxicity.

The first lipid-like molecules to come on the scene were mixtures of cationic and other lipids that would form artificial liposomes. Developed in the late 1980s, liposomal transfection reagents work by enveloping the DNA or RNA and then fusing with the cell membrane to deposit the nucleic acid cargo inside. Roche Applied Science sells liposome formulations based on the cationic lipids DOTAP and DOSPER. Qbiogene's MegaFectin combines DOTAP with different lipids. Under optimized conditions, liposome-mediated methods yield high efficiencies and are much easier to use than calcium phosphate.

Of lipids and polymers

The latest generation of lipid-based transfection products includes multicomponent, nonliposomal reagents consisting of lipids, polymers and combinations thereof. Although their composition is proprietary, most of them work by forming a complex with DNA or RNA that interacts with the cell membrane. The complex is believed to be taken up by endocytosis and then released in the cytoplasm. “Unlike the liposomal agents which form spheres that vary greatly in size, nonliposomal lipids form micelles of uniform size resulting in more reproducible results,” says Jamuna Ramnath, technical service scientist at QIAGEN Inc.

In the lipid arena researchers have a wealth of reagents to choose from. Invitrogen's primary product is Lipofectamine 2000, which works with a variety of nucleic acids and cell lines. It is also applicable to high-throughput screens. “It is quite stable after it makes a complex with DNA, so samples can sit on the deck of a robot loader for a long time,” says Henry Chiou, manager for R&D at Invitrogen Corporation (Box 1).

Roche Applied Sciences' premier transfection reagent is the FuGENE 6 Transfection Reagent, a nonliposomal formulation of proprietary compounds, which has been shown to successfully transfect more than 700 different cell lines. “One of the advantages of FuGENE 6 over other transfection reagents is its broad applicability. It can be used with a wide range of cell lines without optimization and is effective in serum-containing media allowing for a simple consistent method” says product manager, Jeffrey Emch. The reagent also seems to minimize the chance of nonspecific, off-target effects—in other words, effects that are not caused by the transfected DNA or RNA. “We have done studies comparing up- and downregulation of off-target gene expression, and we feel comfortable that FuGENE 6 limits off-target effects,” says Emch. “In an internal study, off-target effects by FuGene 6 were dramatically less than a leading competitive agent.”

In addition to buffering the negative charge on the DNA many reagents also make the cargo smaller to facilitate delivery into cells. InvivoGen's LipoGen combines a lipid that fuses with the cell membrane with spermine, a divalent cationic polyamine that interacts with DNA and condenses it into compact lipid-DNA complexes. Similarly, QIAGEN's Effectene transfection reagent consists of a small positively charged molecule (called 'condensing enhancer') that shrinks the DNA in a dense structure and a nonliposomal lipid that coats the DNA allowing it to interact with the cell surface. Effectene works in the presence of serum and shows low cytotoxicity.

Another line of products that compact DNA includes QIAGEN's SuperFect and PolyFect reagents. They consist of activated spherical molecules (7 nm in diameter) with positively charged tentacles. The DNA coils around these molecules into histone-like structures that can enter the cell by endocytosis. “The dendrimer molecules ensure reproducibility from one experiment to the next,” says Ramnath.

Once they have been taken up by endosomes, the DNA-carrier complexes must escape into the cytosol before being degraded (Box 2). Some carrier molecules are designed to help this process along. Metafectene, distributed by Biontex, is a polycationic transfection reagent based on what the company calls “repulsive membrane acidolysis” technology. When carrier and DNA are taken up in the endosome, the acidic environment induces the carrier to separate from its cargo. Repulsive forces among the positively charged lipophilic parts of the lipids then ease the disruption of the endosomal membrane and, thereby, the release of the genetic material. According to the manufacturers, Megafectene is suitable for high-throughput applications by ensuring high transfection efficiency with small amounts of DNA and reagent.

Amaxa's Nucleofector. (Courtesy of Amaxa.).

Cationic polymers, such as poly(lysine) and poly(ethyleneimine) (PEI), also target release from the endosome. Fermentas' ExGen 500 reagent interacts with DNA to form small, stable, highly diffusible complexes, which are readily endocytosed. The “proton-sponge” effect of ExGen 500 buffers endosomal pH by provoking massive proton accumulation and passive chloride influx. Rapid osmotic swelling causes endosomal rupture, allowing translocation of DNA to the nucleus without DNA degradation. “An important feature is that it works with both primary and secondary cells. There is little to no cytotoxicity,” says Matthew Crouch, product specialist for Fermentas Inc. “It is also cheaper than lipid-based reagents.” Sigma-Aldrich also provides a PEI-based reagent called ESCORT V. Qbiogene has gone a step further by providing PEI-based reagents that couple the carrier molecule to ligands for specific receptors to make it easier to target specific cell types.

Despite the large number of available products, companies are continuing to perfect their blends to produce reagents that can be applied to as broad a spectrum of cells and applications as possible. In particular, many have optimized their transfection reagents to deliver short pieces of RNA to the cytoplasm to silence gene expression (Box 3). Another focus for most companies is to develop better reagents for disease-relevant cells—such as stem cells and human primary cells—which are difficult to transfect. “It is still not a science where can look at a structure and predict what will work best. A lot of the work we do is empirical and requires setting up a variety of screens,” says Invitrogen's Chiou.

Exploiting mother nature

Transfection using lipid- or polymer-based reagents is sometimes referred to as a chemical method, although no chemical reactions are involved, to distinguish it from approaches that use more 'natural' carriers. Nucleic acids can be introduced in cells by hitching a ride on a virus—an approach called transduction. “It is the most efficient system. The virus naturally evolved to get inside cells so it is readily possible to get 90–100% transduction efficiency of primary cells,” says Andrew Farmer, director of cell and molecular biology at Clontech.

A typical transduction protocol involves engineering a viral vector to carry a gene of interest. The vector is then introduced into a packaging cell line to produce recombinant viral particles. The particles are then collected, sometimes purified and titered depending on the application, and used to infect the cells of interest.

The downside of working with viruses is that they present biosafety issues. In addition, transduction protocols may require arduous and time-consuming preparations of vectors and recombinant viruses. New products on the market, however, facilitate the process by providing complete kits that include vector and reporter plasmids, packaging cells, PCR primers as well as all the necessary buffers and solutions.

Clontech sells a broad range of systems for DNA transduction using retroviral and adenoviral vectors, each with its own advantages and disadvantages. Retroviruses insert into the genome of the cell that is transduced and are therefore useful for making stable cell lines, but they can only infect diving cells. Adenoviruses, on the other hand, do not integrate into the genome but can transduce a broad spectrum of cell types with high efficiency. (These two viruses make up the major portion of the viral-vector market.)

A colony of differentiating primary human neural progenitor cells transduced with an adenovirus expressing the DsRed Fluorescent protein. (Courtesy of Clontech.)

In addition to providing complete transduction kits, Clontech sells an adenovirus purification kit. “It is a column that allows you to take the packaging cell lysate and pass it over a filter to produce purified, concentrated virus in about three hours,” says Farmer. The company is developing a similar purification kit for retrovirus. Clontech also sells titration kits that make the determination of the concentrations of infectious virus much easier than with traditional plaque assays.

Lentiviruses, a subclass of retroviruses that includes HIV, are relative new-comers to the viral vector market. Like all retroviruses, they can integrate DNA into host cells, but can infect cells that are not dividing. “They can go into a wider range of cells and create stable cell lines,” says Chiou. “They are continuing to gain popularity.” Invitrogen sells both lentivirus- and adenovirus-based transduction kits.

Adeno-associated virus (AAV)-based systems have also been gaining ground in recent years, in part thanks to kits such as Stratagene's AAV helper-free system. Recombinant AAV are capable of transducing a broad range of both dividing and nondividing cell types, and are less toxic than adenovirus. The major downside of using AAV, however, is that the virus needs to be coinfected with adenovirus to produce recombinant AAV virions in packaging cells. Stratagene's vector system eliminates the need for the helper virus, greatly simplifying the transduction procedure.

Bringing in the guns

When all else fails, electroporation is the brute force approach for delivering genetic material inside cells. Cells suspended in a solution are bombarded with high-voltage pulses of electricity that produce transient holes in the cell membrane, through which the DNA can enter. Electroporation is a harsh technique and many cells will die in the process. For this reason, researchers typically use greater quantities of DNA and cells than with other methods. On the other hand, the technique can be used with almost all types of cells with some success.

Many companies sell electroporators, cuvettes and buffers. Popular instruments include Bio-Rad's Gene Pulser Xcell system and BTX Molecular Delivery Systems' ECM line of electroporators. Recently BTX has released a new product for high-throughput transfections. The BTX HT 96-well electroporation system has a plate handler with auto-track sensing, which allows rapid electroporation of an entire plate using different electrical parameters for all columns, at the press of a button.

The Helios gene gun. (Courtesy of Bio-Rad.)

A welcome twist to the electroporation technique comes from Amaxa. The Nucleofector technology is similar, in principle, to electroporation, but the nucleic acids are delivered directly to the cell's nucleus. The technology is suitable for both DNA and RNA and provides greater viability of transfected cells. “One advantage is that gene expression starts earlier,” says Liz Horton at Amaxa. “It works with primary cells that are typically difficult to transfect by other methods.” Amaxa has over 40 optimized kits and protocols specifically designed for different primary cells, along with five kits that can be optimized for use with the most popular primary mammalian cell types. In addition, Amaxa has optimized protocols for over 50 common cell lines, which use one of five general cell line kits. To assist in the optimization process, the company's website contains a database that lists customers' data.

Several studies have shown that nucleofection is effective in transfecting stem cells, neuronal cells and other primary cells. “Nucleofection worked well in our hands,” says Uma Lakshmipathy at the University of Minnesota Medical School, who used Nucleofector technology to introduce genes into both embryonic and adult stem cells to induce them to differentiate into different lineages. Iversen agrees. “Our experience is that it works very well. The only problem is that you need a lot of cells,” she says. Amaxa is now developing a new 96 well–plate system for high-throughput experiments, which uses small volumes with low cell numbers. “You won't have to have the same parameters for each well,” says Horton. The system allows for each well to be handled independently, using up to 96 different conditions.

In addition to electroporation, several other physical methods to get DNA inside cells exist. About ten years ago Bio-Rad developed an alternative to electroporation with the Helios gene gun, a hand-held device that uses an adjustable low-pressure helium pulse to shoot tiny gold pellets coated with DNA or RNA into cells in tissues. “In electroporation the current causes the membrane to open and an electophoretic effect lets nucleic acid drift in. But the 'biolistic' approach forces the particles in,” says Steve Kulisch, product manager of the gene expression division at Bio-Rad Laboratories. In particular, Bio-Rad's gun has found a niche in genetic vaccination and agriculture applications. A bench-top version of the technology can be used for routine transfections in research labs.

Another physical transfection approach is Magnetofection, a new method that associates nucleic acids or transfection reagents or viruses with cationic magnetic nanoparticles and exploits magnetic force to transport nucleic acids into cells (see also Box 1). According to Oz Biosciences, the company that markets this technology, the complete dose of applied vector is concentrated on the cells within a few minutes and transfection is very efficient for many cell lines including hard-to-transfect ones and primary cells. Oz Biosciences designed four different cationic nanoparticles formulations applied to specific applications: PolyMag can be used with all nucleic acids, including plasmid DNA, RNA, oligonucleotides and short interfering RNA (siRNA); SilenceMag is specifically designed for siRNA delivery; ViroMag is dedicated to viral applications; and CombiMag can be used in combination with transfection reagents to boost their efficacy. “The appeal of the Magnetofection technology is in its versatility toward nucleic acids types, transfection reagents and virus, its efficiency and universitality in cells successfully tested,” says Olivier Zephati, CEO of Oz Biosciences.

When it comes to delivering nucleic acids inside cells, options abound. The advice most researchers give is to test several reagents or techniques by setting up a matrix of conditions. For this purpose, many companies sell optimization kits and trial-sized aliquots or even provide researchers with free samples to try. In addition, the websites of companies that supply transfection reagents often contain databases of transfection protocols for different cell types and applications. (Table 1)

Table 1 Suppliers guide: companies offering flow cytometry products and services

References

  1. Graham, F.L. & van der Eb, A.J. Virology 54, 536–539 (1973).

    CAS  Article  Google Scholar 

  2. McCutchan, J.H. & Pagano, J.S. J. Natl. Cancer Inst. 41, 351–357 (1968).

    CAS  PubMed  Google Scholar 

  3. Ziauddin, J. & Sabatini, D.M. Nature 411, 107–110 (2001).

    CAS  Article  Google Scholar 

  4. Isalan, M. et al. Nat. Methods 2, 113–118 (2005).

    CAS  Article  Google Scholar 

  5. Isalan, M. et al. PLoS Biol. 3, e104 (2005).

    Article  Google Scholar 

  6. Berg, K. et al. Cancer Res. 59, 1180–1183 (1999).

    CAS  PubMed  Google Scholar 

Download references

Author information

Author notes

  1. Laura Bonetta is a freelance writer based in the Washington, DC area.

    • Laura Bonetta
Authors

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Bonetta, L. The inside scoop—evaluating gene delivery methods. Nat Methods 2, 875–883 (2005). https://doi.org/10.1038/nmeth1105-875

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1038/nmeth1105-875

Further reading

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing