1 00:00:06,840 --> 00:00:07,450 INSTRUCTOR: Good morning. 2 00:00:07,450 --> 00:00:09,980 Good morning. 3 00:00:09,980 --> 00:00:14,630 So, anybody check The New York Times yesterday? 4 00:00:17,390 --> 00:00:18,413 What did you see? 5 00:00:18,413 --> 00:00:19,663 AUDIENCE: [INAUDIBLE] 6 00:00:27,590 --> 00:00:29,154 INSTRUCTOR: People, what people? 7 00:00:29,154 --> 00:00:31,050 AUDIENCE: I can't remember their names. 8 00:00:31,050 --> 00:00:31,524 [INAUDIBLE] 9 00:00:31,524 --> 00:00:31,998 INSTRUCTOR: [LAUGHS] 10 00:00:31,998 --> 00:00:33,248 AUDIENCE: [INAUDIBLE] 11 00:00:35,316 --> 00:00:36,750 I can't remember their names. 12 00:00:36,750 --> 00:00:38,870 INSTRUCTOR: Yeah, the Crick and Watson people. 13 00:00:38,870 --> 00:00:40,060 AUDIENCE: [INAUDIBLE]. 14 00:00:40,060 --> 00:00:41,030 INSTRUCTOR: Exactly. 15 00:00:41,030 --> 00:00:44,230 So, perfect timing, The New York Times had an article in 16 00:00:44,230 --> 00:00:47,570 yesterday's paper. 17 00:00:47,570 --> 00:00:52,130 Francis Crick's correspondence with Maurice Wilkins during 18 00:00:52,130 --> 00:00:56,430 the critical year when Crick and Watson went down and saw 19 00:00:56,430 --> 00:00:58,100 the X-ray crystallography. 20 00:00:58,100 --> 00:00:59,190 By the way, I made a mistake. 21 00:00:59,190 --> 00:01:03,650 I said that Rosalind Franklin showed it to Crick and Watson. 22 00:01:03,650 --> 00:01:06,795 Actually it was Maurice Wilkins who showed it to Crick 23 00:01:06,795 --> 00:01:09,330 and Watson when Rosalind Franklin was away. 24 00:01:09,330 --> 00:01:13,380 Which, was itself a slightly complicated thing to be doing 25 00:01:13,380 --> 00:01:15,670 because it was really Rosalind Franklin's work. 26 00:01:15,670 --> 00:01:18,200 But in any case, there was correspondence, some heated 27 00:01:18,200 --> 00:01:21,230 correspondence that went back between Crick 28 00:01:21,230 --> 00:01:24,900 and Wilkins and others. 29 00:01:24,900 --> 00:01:29,020 And it was believed that the correspondence had been lost, 30 00:01:29,020 --> 00:01:30,860 had been thrown out. 31 00:01:30,860 --> 00:01:34,690 But in fact, it turns out that in the papers of Sydney 32 00:01:34,690 --> 00:01:39,130 Brenner, another great person of that period, Crick's 33 00:01:39,130 --> 00:01:42,750 correspondence had got misfiled in Sydney's files. 34 00:01:42,750 --> 00:01:45,450 Sydney had donated his files to the Cold Spring Harbor 35 00:01:45,450 --> 00:01:47,190 Laboratory on Long Island. 36 00:01:47,190 --> 00:01:49,360 And they went through the files in the past several 37 00:01:49,360 --> 00:01:51,270 months and found them. 38 00:01:51,270 --> 00:01:53,990 So we actually now have, as The New York Times reported 39 00:01:53,990 --> 00:01:59,340 yesterday, the letters with Crick and Watson and Maurice 40 00:01:59,340 --> 00:02:03,200 Wilkins about just that period I was telling you about. 41 00:02:03,200 --> 00:02:06,150 It doesn't radically change any of the story. 42 00:02:06,150 --> 00:02:08,280 But it really shows you the attitude. 43 00:02:08,280 --> 00:02:10,389 And if you read the New York Times article, you'll find all 44 00:02:10,389 --> 00:02:13,550 sorts of juicy quotes about the attitude back and forth 45 00:02:13,550 --> 00:02:17,210 there, including the first model Crick and Watson made 46 00:02:17,210 --> 00:02:19,790 where they totally screwed up because they had misunderstood 47 00:02:19,790 --> 00:02:21,370 some number. 48 00:02:21,370 --> 00:02:24,150 Anyway, it's interesting stuff. 49 00:02:24,150 --> 00:02:27,820 And the reason I bring up this history is because science is 50 00:02:27,820 --> 00:02:29,340 done by real people. 51 00:02:29,340 --> 00:02:30,920 It's a business of passion. 52 00:02:30,920 --> 00:02:33,130 It's a business of trying to-- you know -- 53 00:02:33,130 --> 00:02:34,560 science is wonderful. 54 00:02:34,560 --> 00:02:35,720 It's objective in a certain sense. 55 00:02:35,720 --> 00:02:38,346 And it's also about convincing others. 56 00:02:38,346 --> 00:02:40,830 You know, a scientific result doesn't mean anything unless 57 00:02:40,830 --> 00:02:42,580 you can convince the community. 58 00:02:42,580 --> 00:02:45,730 So it's an inherently human activity to bring people's 59 00:02:45,730 --> 00:02:48,240 attention to things, make things clear. 60 00:02:48,240 --> 00:02:50,400 Anyway, that was kind of cool. 61 00:02:50,400 --> 00:02:54,160 I invite you all to go look at The Times article. 62 00:02:54,160 --> 00:02:57,490 You don't realize how much work we have to go to in 7.01 63 00:02:57,490 --> 00:02:59,990 to arrange these things to come out just at the right 64 00:02:59,990 --> 00:03:02,250 time during our curriculum. 65 00:03:02,250 --> 00:03:06,070 But we pay off The New York Times and they do our bidding. 66 00:03:06,070 --> 00:03:11,530 So last time we were talking about-- 67 00:03:11,530 --> 00:03:16,810 I want to briefly go back to the Semiconservative Model, 68 00:03:16,810 --> 00:03:23,010 which I ended with last time, of DNA replication, the work 69 00:03:23,010 --> 00:03:26,110 of Matt Meselson and Frank Stahl, these graduate students 70 00:03:26,110 --> 00:03:27,300 at Caltech. 71 00:03:27,300 --> 00:03:30,680 So you remember, our DNA double helix immediately 72 00:03:30,680 --> 00:03:34,520 suggests the secret of life, the way that you copy 73 00:03:34,520 --> 00:03:36,480 information to daughter cells. 74 00:03:36,480 --> 00:03:40,210 Each strand is a sufficient template for the other strand. 75 00:03:40,210 --> 00:03:46,830 If you just unzipped them, each would be able to serve as 76 00:03:46,830 --> 00:03:50,850 a template for replication for the other strand. 77 00:03:50,850 --> 00:03:51,420 Beautiful. 78 00:03:51,420 --> 00:03:55,420 It's called Semiconservative because you've conserved. 79 00:03:55,420 --> 00:03:57,180 You used one strand. 80 00:03:57,180 --> 00:03:59,300 And you've made a new strand on the other. 81 00:04:01,940 --> 00:04:03,950 It seems obvious, but we can't take things 82 00:04:03,950 --> 00:04:05,190 for obvious in science. 83 00:04:05,190 --> 00:04:08,800 Because the alternative model, alternative, which we know 84 00:04:08,800 --> 00:04:12,610 today is of course wrong, is that somehow the cell comes 85 00:04:12,610 --> 00:04:20,079 along, feels this double helix as a template, and somehow 86 00:04:20,079 --> 00:04:24,000 builds two new strands that are the same 87 00:04:24,000 --> 00:04:24,930 as that double helix. 88 00:04:24,930 --> 00:04:27,930 They build a new double helix with both strands being new. 89 00:04:27,930 --> 00:04:28,590 That's nuts-- 90 00:04:28,590 --> 00:04:29,350 why would you do it? 91 00:04:29,350 --> 00:04:31,530 It's so obvious you could use one strand as the 92 00:04:31,530 --> 00:04:32,630 template for the other. 93 00:04:32,630 --> 00:04:35,420 But this is what Meselson and Stahl had to rule out. 94 00:04:35,420 --> 00:04:39,230 They had to rule out that that double helix stayed intact, 95 00:04:39,230 --> 00:04:41,980 and maybe the cell sent some enzymes around to feel its 96 00:04:41,980 --> 00:04:46,500 shape and somehow construct another double helix like it. 97 00:04:46,500 --> 00:04:48,690 That would be a non-conservative model. 98 00:04:48,690 --> 00:04:50,900 You weren't using any old strands. 99 00:04:50,900 --> 00:04:52,370 The two old strands stayed together. 100 00:04:52,370 --> 00:04:54,010 And you made two new strands. 101 00:04:54,010 --> 00:04:56,810 That's what they were trying to distinguish between, this 102 00:04:56,810 --> 00:04:58,910 semiconservative model or not. 103 00:04:58,910 --> 00:05:04,300 So I just remind you that their really cool, cool idea-- 104 00:05:04,300 --> 00:05:08,650 see, they couldn't use a radioactive tracer that was 105 00:05:08,650 --> 00:05:11,140 different on the new strand than the old strand in the 106 00:05:11,140 --> 00:05:12,710 conventional sense. 107 00:05:12,710 --> 00:05:15,730 Because, of course, they're made out of the same atoms. 108 00:05:15,730 --> 00:05:20,860 But what they did do, as we talked about last time, was 109 00:05:20,860 --> 00:05:22,880 they take the DNA. 110 00:05:22,880 --> 00:05:27,020 They grow it up in heavy nitrogen. 111 00:05:27,020 --> 00:05:30,570 They then shift the bacteria to light nitrogen. 112 00:05:34,900 --> 00:05:42,970 And, if in fact the Semiconservative Model is 113 00:05:42,970 --> 00:05:47,290 right, then the new DNA after one generation of growth will 114 00:05:47,290 --> 00:05:48,940 have a lighter density. 115 00:05:48,940 --> 00:05:52,530 Very simple, except that they had to go invent a way to 116 00:05:52,530 --> 00:05:53,920 measure density. 117 00:05:53,920 --> 00:05:57,250 They had to invent this centrifugation process where 118 00:05:57,250 --> 00:05:59,780 they spin really, really, really, really hard. 119 00:05:59,780 --> 00:06:02,560 And the salt gets a little denser here, and a little less 120 00:06:02,560 --> 00:06:04,380 dense here, and a little less dense here. 121 00:06:04,380 --> 00:06:06,430 And it's not a very huge difference. 122 00:06:06,430 --> 00:06:09,880 But if you know the density of DNA, and you arrange your salt 123 00:06:09,880 --> 00:06:13,190 concentration at just the right density, you can spin it 124 00:06:13,190 --> 00:06:16,710 really hard so that there's some gradient in 125 00:06:16,710 --> 00:06:18,550 density in the salt. 126 00:06:18,550 --> 00:06:23,740 And the heavier stuff will band here. 127 00:06:23,740 --> 00:06:26,010 The lighter stuff from one generation of 128 00:06:26,010 --> 00:06:29,260 growth will band there. 129 00:06:29,260 --> 00:06:35,420 And normal DNA would band there. 130 00:06:35,420 --> 00:06:37,110 And that's a pretty convincing proof. 131 00:06:37,110 --> 00:06:39,950 After no generations it's all in 15-15. 132 00:06:39,950 --> 00:06:41,900 After one generation it's all intermediate. 133 00:06:41,900 --> 00:06:45,110 After two generations some of it is now 14-14. 134 00:06:45,110 --> 00:06:47,050 Some of it is 14-15. 135 00:06:47,050 --> 00:06:48,590 And onward like that. 136 00:06:48,590 --> 00:06:51,200 Obvious, and it's a gorgeous experiment, just a gorgeous 137 00:06:51,200 --> 00:06:51,780 experiment. 138 00:06:51,780 --> 00:06:55,420 And this idea of density centrifugation, which they 139 00:06:55,420 --> 00:06:57,930 invented for this purpose, has been used for many other 140 00:06:57,930 --> 00:06:59,180 purposes since.