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Large structural scaffold formed by the multi-domain core enzyme, E2, aLarge structural scaffold formed by the multi-domain core enzyme, E2, a specific dihydrolipoyl acetyltransferase. The E2 polypeptide chain is composed of three independently folded domains separated by flexible linker regions: a lypoil domain (LD) of 9.5 kDa, a peripheral (E1 and/or E3) subunit-binding domain (PSBD) of 5.
Large structural scaffold formed by the multi-domain core enzyme, E2, aLarge structural scaffold formed by the multi-domain core enzyme, E2, a specific dihydrolipoyl acetyltransferase. The E2 polypeptide chain is composed of three independently folded domains separated by flexible linker regions: a lypoil domain (LD) of 9.5 kDa, a peripheral (E1 and/or E3) subunit-binding domain (PSBD) of 5.
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Ve response without requiring multiple booster shoots, thus significantly reducing theVe response without requiring multiple booster shoots, thus significantly reducing the vaccine costs. VLPs do not need attenuation or inactivation - as the live attenuated and killed/ inactivated vaccines - avoiding all the possible side effects of inactivation treatments on the epitope modifications. Moreo
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I54A A50S K51Ea b1.6 m2.4 m2.4 m14.7 47.4.1 40.10.8 62.3 40.4 59.9.2 38.6 26.5 18.Data from the experiment shown in Fig. 4, B and C. Data from the experiment shown in Fig. 5, B and C.FIGURE 6. Correlation between the percentage of 32 that remains free in gel filtration analysis and the stability of 32 (half-life) in vivo. Gel filtration experiments were repeated 2?4 times, and the percentages of
I54A A50S K51Ea b1.6 m2.4 m2.4 m14.7 47.4.1 40.10.8 62.3 40.4 59.9.2 38.6 26.5 18.Data from the experiment shown in Fig. 4, B and C. Data from the experiment shown in Fig. 5, B and C.FIGURE 6. Correlation between the percentage of 32 that remains free in gel filtration analysis and the stability of 32 (half-life) in vivo. Gel filtration experiments were repeated 2?4 times, and the percentages of
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Icity of the liposomal surface, and/or by encapsulating additional adjuvantsIcity of the liposomal surface, and/or by encapsulating additional adjuvants ("conventional" and second-generation liposomes, the [44-46] stealth technology ). Since liposomes were first described in 1960, these nanoparticulate carriers were investigated for various purposes - including industrial, pharmaceutical, cl
2, A and B), these results clearly indicate that amino acid substitutions in Region 2.1 resulted in a reduced affinity for DnaJ specifically.VOLUME 287 ?NUMBER 23 ?JUNE 1,19278 JOURNAL OF BIOLOGICAL CHEMISTRYChaperone Binding toFIGURE 3. Pull-down assay for complex formed between DnaK-His or DnaJ-His and 32. A, 32 (4 M) was incubated with DnaK-His (2 M) at 30 for 30 min in the absence ( ) or in
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