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Experiment Module (JEM), where the samples are kept   pathogen, and other enzymes in the DPP family,
               for a period of 1 to 2 months at a stable temperature,   the substance would become an antimicrobial agent.
               20°C (68°F). A counter-diffusion method called the   Thus, the research team also decided to develop
               Gel-Tube method is used for crystallization whereby   antimicrobial agents.
               polyethylene glycol or salt solution is diffused into   Several types of DPPs exist, and each one works
               the protein solution, which is separated by a porous   differently. For example, DAP BII (DPP7) recognizes
               membrane inside a tube. In this method, concentration   and cleaves hydrophobic or basic amino acids.
               of polyethylene glycol in the protein solution gradually   On the other hand, DPP11 recognizes acidic amino
               increases and finally satisfies the condition for protein   acids. These enzymes are not found in humans, they
               crystallization. In addition to the existing experiments   are only found in microorganisms. In other words, if you
               conducted at 20°C (68°F), experiments at 4°C (40°F)   can make medicines to suppress the function of these
               are now being started. Crystallization at 4°C (40°F)   enzymes, it is harmless for humans and only suppresses
               realizes the crystallization of candidate drugs in high   the growth of bacteria. If the peptide binding mode of
               demand, such as unstable hydrosoluble proteins    protein is clarified in detail, a new drug could be created
               and membrane proteins.
                                                               that targets only DPP of microorganisms, but has no
               During the ISS PCG experiments, the crystal structure   effect on humans.
               of the dipeptidyl peptidase 7 (DPP) was discovered
               for Antimicrobial Agent Development. Dr. Yasumitsu
               Sakamoto of Iwate Medical University used the
               microgravity environment aboard the ISS for JAXA
               PCG experiments. Dr. Sakamoto explains this newly
               discovered enzyme: In the course of the research,
               this enzyme, named DAP BII (DPP7), was found to
               be important for the proliferation and growth of a group
               of bacteria: Non-Fermenting Gram Negative Rods
               (NFGNR), which live by using peptides and proteins as
               their nutrients. NFGNR includes the causative bacteria
               of periodontal disease and hospital-acquired infection.
               Incidentally, periodontal disease is the most widespread
               infectious disease among human beings. When he
               started this study, he considered this enzyme to be
               both unusual and interesting. Then Dr. Sakamoto also
               considered that if a substance could inhibit the function
               of DAP BII (DPP7), which is essential for growth of the


                                                                  Substrate specificity of the DPP family.
                                                                  Image credit: Iwate Medical University




                                                               Following the discovery of DPP7, the researchers are
                                                               keeping on analyzing the structure of DPP11 to use it as
                                                               a target for antibiotics. The present analyses of DPP11
                                                               structure could be useful templates for the design of
                                                               specific inhibitors of DPP11 from pathogenic organisms.
                                                               In terms of application, researchers aim to develop
                                                               antibacterial drugs. Scientifically, they will keep going
                                                               to elucidate the entire mechanism of peptide uptake.
                  Expected mechanism of peptide uptake of NFGNR.   For more information, visit the following link:
                                                               http://iss.jaxa.jp/kiboexp/theme/first/protein/en/
                  Image credit: Iwate Medical University
                                                               interview/interview02.html#main




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