A single line often inverts meaning once you see what it
answers, so neighbouring messages are always shown.
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And that was your decision, solely. No one encourage you or suggested?
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Nobody encouraged me or suggested it. In this case I approached the journal because, again, going back to the transmissible flu studies, it was not just the creation of the transmissible flu virus that was considered sensitive information. It was the details of the technology which also was dual-use. So it's not necessarily just the creation of the entity or the pathogen that's gain-or-function or dual-use. The methodology can be sensitive, and I felt that it was best that we did not provide that information. So that's one example.
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Okay.
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The second example, which is the reason why I'm reluctant to talk about it here, because I do not want to be responsible as the one who releases it to the public. If you all choose to do that then you can accept the responsibility of that. Sometimes in science you come across findings that are potentially concerning. And so in this case, Fang Li had been doing studies using biochemical approaches to identify DC.Scheduling@LexitasLegal.com the most optimal receptor binding domain possible to grab either the human ACE2 receptor or the mouse ACE2 receptor. The thought in the field from him, as a biochemist, was that would be the most optimal and most dangerous form of virus. I disagreed with him, because in reality, biochemical interactions are, in essence, a bell-shaped curve. If they can't interact very well, the virus can't get in. If they react too well, that interaction can't come apart. So the virus can't get in, and the virus, as it tries to release, gets caught up in what's called a dominant negative effect, and it will prevent virus replication. And the reason I knew this is I had overexpressed receptors before, with mouse hepatitis virus. And because there was so much receptor there, the virus, as it got in, it replicated fine, but when it came out all the spikes were stripped off of the particle. So if the interaction is too great it kills the virus. Anyone who might want to do nefarious work in science, wanted to create something, is going to think that the most efficient interaction is where you want to go. So I tested that hypothesis and showed that I was right, that the super-binding things were just as deleterious as the really poor-binding ones. I subsequently told NIH and destroyed those viruses. I have never told anyone, and I would DC.Scheduling@LexitasLegal.com recommend that this committee not release that, because then you will be responsible for telling terrorists what to do.
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2026-04-10 09:00
Christina Salazar
Are you aware of ?
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That's a shock to me. No, I was not.
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Okay.
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Yeah. Again, this would have been -- there would never have been any sharing of data with him. It would have been uncommon. In fact, it was surprising to me that about a month ago he actually raised the topic with me, "Do you think maybe that if we had super, high-affinity binding that might not be good?" I just said I didn't -- yeah, so.
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And those are the only two?