The cyclol hypothesis is the first structural model of a folded, globular protein. It was developed by Dorothy Wrinch in the late 1930s, and was based on three assumptions. Firstly, the hypothesis assumes that two peptide groups can be crosslinked by a cyclol reaction (Figure 1); these crosslinks are covalent analogs of non-covalent hydrogen bonds between peptide groups. These reactions have been observed in the ergopeptides and other compounds. Secondly, it assumes that, under some conditions, amino acids will naturally make the maximum possible number of cyclol crosslinks, resulting in cyclol molecules (Figure 2) and cyclol fabrics (Figure 3). These cyclol molecules and fabrics have never been observed. Finally, the hypothesis assumes that globular proteins have a tertiary structure corresponding to Platonic solids and semiregular polyhedra formed of cyclol fabrics with no free edges. Such "closed cyclol" molecules have not been observed either.
Although later data demonstrated that this original model for the structure of globular proteins needed to be amended, several elements of the cyclol model were verified, such as the cyclol reaction itself and the hypothesis that hydrophobic interactions are chiefly responsible for protein folding. The cyclol hypothesis stimulated many scientists to research questions in protein structure and chemistry, and was a precursor of the more accurate models hypothesized for the DNA double helix and protein secondary structure. The proposal and testing of the cyclol model also provides an excellent illustration of empirical falsifiability acting as part of the scientific method.
By the mid-1930s, analytical ultracentrifugation studies by Theodor Svedberg had shown that proteins had a well-defined chemical structure, and were not aggregations of small molecules. The same studies appeared to show that the molecular weight of proteins fell into a few well-defined classes related by integers, such as Mw = 2p3q Da, where p and q are nonnegative integers. However, it was difficult to determine the exact molecular weight and number of amino acids in a protein. Svedberg had also shown that a change in solution conditions could cause a protein to disassemble into small subunits, now known as a change in quaternary structure.
The chemical structure of proteins was still under debate at that time. The most accepted (and ultimately correct) hypothesis was that proteins are linear polypeptides, i.e., unbranched polymers of amino acids linked by peptide bonds. However, a typical protein is remarkably long—hundreds of amino-acid residues—and several distinguished scientists were unsure whether such long, linear macromolecules could be stable in solution. Further doubts about the polypeptide nature of proteins arose because some enzymes were observed to cleave proteins but not peptides, whereas other enzymes cleave peptides but not folded proteins. Attempts to synthesize proteins in the test tube were unsuccessful, mainly due to the chirality of amino acids; naturally occurring proteins are composed of only left-handed amino acids. Hence, alternative chemical models of proteins were considered, such as the diketopiperazine hypothesis of Emil Abderhalden. However, no alternative model had yet explained why proteins yield only amino acids and peptides upon hydrolysis and proteolysis. As clarified by Linderstrøm-Lang, these proteolysis data showed that denatured proteins were polypeptides, but no data had yet been obtained about the structure of folded proteins; thus, denaturation could involve a chemical change that converted folded proteins into polypeptides.
The process of protein denaturation (as distinguished from coagulation) had been discovered in 1910 by Harriette Chick and Charles Martin, but its nature was still mysterious. Tim Anson and Alfred Mirsky had shown that denaturation was a reversible, two-state process that results in many chemical groups becoming available for chemical reactions, including cleavage by enzymes. In 1929, Hsien Wu hypothesized correctly that denaturation corresponded to protein unfolding, a purely conformational change that resulted in the exposure of amino-acid side chains to the solvent. Wu's hypothesis was also advanced independently in 1936 by Mirsky and Linus Pauling. Nevertheless, protein scientists could not exclude the possibility that denaturation corresponded to a chemical change in the protein structure, a hypothesis that was considered a (distant) possibility until the 1950s.
X-ray crystallography had just begun as a discipline in 1911, and had advanced relatively rapidly from simple salt crystals to crystals of complex molecules such as cholesterol. However, even the smallest proteins have over 1000 atoms, which makes determining their structure far more complex. In 1934, Dorothy Crowfoot Hodgkin had taken crystallographic data on the structure of the small protein, insulin, although the structure of that and other proteins were not solved until the late 1960s. However, pioneering X-ray fiber diffraction data had been collected in the early 1930s for many natural fibrous proteins such as wool and hair by William Astbury, who proposed rudimentary models of secondary structure elements such as the alpha helix and the beta sheet.
Since protein structure was so poorly understood in the 1930s, the physical interactions responsible for stabilizing that structure were likewise unknown. Astbury hypothesized that the structure of fibrous proteins was stabilized by hydrogen bonds in β-sheets. The idea that globular proteins are also stabilized by hydrogen bonds was proposed by Dorothy Jordan Lloyd in 1932, and championed later by Alfred Mirsky and Linus Pauling. At a 1933 lecture by Astbury to the Oxford Junior Scientific Society, physicist Frederick Frank suggested that the fibrous protein α-keratin might be stabilized by an alternative mechanism, namely, covalent crosslinking of the peptide bonds by the cyclol reaction above. The cyclol crosslink draws the two peptide groups close together; the N and C atoms are separated by ~1.5 Å, whereas they are separated by ~3 Å in a typical hydrogen bond. The idea intrigued J. D. Bernal, who suggested it to the mathematician Dorothy Wrinch as possibly useful in understanding protein structure.
Wrinch developed this suggestion into a full-fledged model of protein structure. The basic cyclol model was laid out in her first paper (1936). She noted the possibility that polypeptides might cyclize to form closed rings (true) and that these rings might form internal crosslinks through the cyclol reaction (also true, although rare). Assuming that the cyclol form of the peptide bond could be more stable than the amide form, Wrinch concluded that certain cyclic peptides would naturally make the maximal number of cyclol bonds (such as cyclol 6, Figure 2). Such cyclol molecules would have hexagonal symmetry, if the chemical bonds were taken as having the same length, roughly 1.5 Å; for comparison, the N-C and C-C bonds have the lengths 1.42 Å and 1.54 Å, respectively.
These rings can be extended indefinitely to form a cyclol fabric (Figure 3). Such fabrics exhibit a long-range, quasi-crystalline order that Wrinch felt was likely in proteins, since they must pack hundreds of residues densely. Another interesting feature of such molecules and fabrics is that their amino-acid side chains point axially upwards from only one face; the opposite face has no side chains. Thus, one face is completely independent of the primary sequence of the peptide, which Wrinch conjectured might account for sequence-independent properties of proteins.
In her initial article, Wrinch stated clearly that the cyclol model was merely a working hypothesis, a potentially valid model of proteins that would have to be checked. Her goals in this article and its successors were to propose a well-defined testable model, to work out the consequences of its assumptions and to make predictions that could be tested experimentally. In these goals, she succeeded; however, within a few years, experiments and further modeling showed that the cyclol hypothesis was untenable as a model for globular proteins.
In two tandem Letters to the Editor (1936), Wrinch and Frank addressed the question of whether the cyclol form of the peptide group was indeed more stable than the amide form. A relatively simple calculation showed that the cyclol form is significantly less stable than the amide form. Therefore, the cyclol model would have to be abandoned unless a compensating source of energy could be identified. Initially, Frank proposed that the cyclol form might be stabilized by better interactions with the surrounding solvent; later, Wrinch and Irving Langmuir hypothesized that hydrophobic association of nonpolar sidechains provides stabilizing energy to overcome the energetic cost of the cyclol reactions.
The lability of the cyclol bond was seen as an advantage of the model, since it provided a natural explanation for the properties of denaturation; reversion of cyclol bonds to their more stable amide form would open up the structure and allows those bonds to be attacked by proteases, consistent with experiment. Early studies showed that proteins denatured by pressure are often in a different state than the same proteins denatured by high temperature, which was interpreted as possibly supporting the cyclol model of denaturation.
The Langmuir-Wrinch hypothesis of hydrophobic stabilization shared in the downfall of the cyclol model, owing mainly to the influence of Linus Pauling, who favored the hypothesis that protein structure was stabilized by hydrogen bonds. Another twenty years had to pass before hydrophobic interactions were recognized as the chief driving force in protein folding.
In her third paper on cyclols (1936), Wrinch noted that many "physiologically active" substances such as steroids are composed of fused hexagonal rings of carbon atoms and, thus, might be sterically complementary to the face of cyclol molecules without the amino-acid side chains. Wrinch proposed that steric complementarity was one of chief factors in determining whether a small molecule would bind to a protein.
Wrinch speculated that proteins are responsible for the synthesis of all biological molecules. Noting that cells digest their proteins only under extreme starvation conditions, Wrinch further speculated that life could not exist without proteins.
From the beginning, the cyclol reaction was considered as a covalent analog of the hydrogen bond. Therefore, it was natural to consider hybrid models with both types of bonds. This was the subject of Wrinch's fourth paper on the cyclol model (1936), written together with Dorothy Jordan Lloyd, who first proposed that globular proteins are stabilized by hydrogen bonds. A follow-up paper was written in 1937 that referenced other researchers on hydrogen bonding in proteins, such as Maurice Loyal Huggins and Linus Pauling.
Wrinch also wrote a paper with William Astbury, noting the possibility of a keto-enol isomerization of the >CαHα and an amide carbonyl group >C=O, producing a crosslink >Cα-C(OHα)< and again converting the oxygen to a hydroxyl group. Such reactions could yield five-membered rings, whereas the classic cyclol hypothesis produces six-membered rings. This keto-enol crosslink hypothesis was not developed much further.
In her fifth paper on cyclols (1937), Wrinch identified the conditions under which two planar cyclol fabrics could be joined to make an angle between their planes while respecting the chemical bond angles. She identified a mathematical simplification, in which the non-planar six-membered rings of atoms can be represented by planar "median hexagon"s made from the midpoints of the chemical bonds. This "median hexagon" representation made it easy to see that the cyclol fabric planes can be joined correctly if the dihedral angle between the planes equals the tetrahedral bond angle δ = arccos(-1/3) ≈ 109.47°.
A large variety of closed polyhedra meeting this criterion can be constructed, of which the simplest are the truncated tetrahedron, the truncated octahedron, and the octahedron, which are Platonic solids or semiregular polyhedra. Considering the first series of "closed cyclols" (those modeled on the truncated tetrahedron), Wrinch showed that their number of amino acids increased quadratically as 72n2, where n is the index of the closed cyclol Cn. Thus, the C1 cyclol has 72 residues, the C2 cyclol has 288 residues, etc. Preliminary experimental support for this prediction came from Max Bergmann and Carl Niemann, whose amino-acid analyses suggested that proteins were composed of integer multiples of 288 amino-acid residues (n=2). More generally, the cyclol model of globular proteins accounted for the early analytical ultracentrifugation results of Theodor Svedberg, which suggested that the molecular weights of proteins fell into a few classes related by integers.
The cyclol model was consistent with the general properties then attributed to folded proteins. (1) Centrifugation studies had shown that folded proteins were significantly denser than water (~1.4 g/mL) and, thus, tightly packed; Wrinch assumed that dense packing should imply regular packing. (2) Despite their large size, some proteins crystallize readily into symmetric crystals, consistent with the idea of symmetric faces that match up upon association. (3) Proteins bind metal ions; since metal-binding sites must have specific bond geometries (e.g., octahedral), it was plausible to assume that the entire protein also had similarly crystalline geometry. (4) As described above, the cyclol model provided a simple chemical explanation of denaturation and the difficulty of cleaving folded proteins with proteases. (5) Proteins were assumed to be responsible for the synthesis of all biological molecules, including other proteins. Wrinch noted that a fixed, uniform structure would be useful for proteins in templating their own synthesis, analogous to the Watson-Francis Crick concept of DNA templating its own replication. Given that many biological molecules such as sugars and sterols have a hexagonal structure, it was plausible to assume that their synthesizing proteins likewise had a hexagonal structure. Wrinch summarized her model and the supporting molecular-weight experimental data in three review articles.
Predicted protein structures
Having proposed a model of globular proteins, Wrinch investigated whether it was consistent with the available structural data. She hypothesized that bovine tuberculin protein (523) was a C1 closed cyclol consisting of 72 residues and that the digestive enzyme pepsin was a C2 closed cyclol of 288 residues. These residue-number predictions were difficult to verify, since the methods then available to measure the mass of proteins were inaccurate, such as analytical ultracentrifugation and chemical methods.
Wrinch also predicted that insulin was a C2 closed cyclol consisting of 288 residues. Limited X-ray crystallographic data were available for insulin which Wrinch interpreted as "confirming" her model. However, this interpretation drew rather severe criticism for being premature. Careful studies of the Patterson diagrams of insulin taken by Dorothy Crowfoot Hodgkin showed that they were roughly consistent with the cyclol model; however, the agreement was not good enough to claim that the cyclol model was confirmed.
The cyclol fabric was shown to be implausible for several reasons. Hans Neurath and Henry Bull showed that the dense packing of side chains in the cyclol fabric was inconsistent with the experimental density observed in protein films. Maurice Huggins calculated that several non-bonded atoms of the cyclol fabric would approach more closely than allowed by their van der Waals radii; for example, the inner Hα and Cα atoms of the lacunae would be separated by only 1.68 Å (Figure 5). Haurowitz showed chemically that the outside of proteins could not have a large number of hydroxyl groups, a key prediction of the cyclol model, whereas Meyer and Hohenemser showed that cyclol condensations of amino acids did not exist even in minute quantities as a transition state. More general chemical arguments against the cyclol model were given by Bergmann and Niemann and by Neuberger. Infrared spectroscopic data showed that the number of carbonyl groups in a protein did not change upon hydrolysis, and that intact, folded proteins have a full complement of amide carbonyl groups; both observations contradict the cyclol hypothesis that such carbonyls are converted to hydroxyl groups in folded proteins. Finally, proteins were known to contain proline in significant quantities (typically 5%); since proline lacks the amide hydrogen and its nitrogen already forms three covalent bonds, proline seems incapable of the cyclol reaction and of being incorporated into a cyclol fabric. An encyclopedic summary of the chemical and structural evidence against the cyclol model was given by Pauling and Niemann. Moreover, a supporting piece of evidence—the result that all proteins contain an integer multiple of 288 amino-acid residues—was likewise shown to be incorrect in 1939.
Wrinch replied to the steric-clash, free-energy, chemical and residue-number criticisms of the cyclol model. On steric clashes, she noted that small deformations of the bond angles and bond lengths would allow these steric clashes to be relieved, or at least reduced to a reasonable level. She noted that distances between non-bonded groups within a single molecule can be shorter than expected from their van der Waals radii, e.g., the 2.93 Å distance between methyl groups in hexamethylbenzene. Regarding the free-energy penalty for the cyclol reaction, Wrinch disagreed with Pauling's calculations and stated that too little was known of intramolecular energies to rule out the cyclol model on that basis alone. In reply to the chemical criticisms, Wrinch suggested that the model compounds and simple bimolecular reactions studied need not pertain to the cyclol model, and that steric hindrance may have prevented the surface hydroxyl groups from reacting. On the residue-number criticism, Wrinch extended her model to allow for other numbers of residues. In particular, she produced a "minimal" closed cyclol of only 48 residues, and, on that (incorrect) basis, may have been the first to suggest that the insulin monomer had a molecular weight of roughly 6000 Da.
Therefore, she maintained that the cyclol model of globular proteins was still potentially viable and even proposed the cyclol fabric as a component of the cytoskeleton. However, most protein scientists ceased to believe in it and Wrinch turned her scientific attention to mathematical problems in X-ray crystallography, to which she contributed significantly. One exception was physicist Gladys Anslow, Wrinch's colleague at Smith College, who studied the ultraviolet absorption spectra of proteins and peptides in the 1940s and allowed for the possibility of cyclols in interpreting her results. As the sequence of insulin began to be determined by Frederick Sanger, Anslow published a three-dimensional cyclol model with sidechains, based on the backbone of Wrinch's 1948 "minimal cyclol" model.
The downfall of the overall cyclol model generally led to a rejection of its elements; one notable exception was J. D. Bernal's short-lived acceptance of the Langmuir-Wrinch hypothesis that protein folding is driven by hydrophobic association. Nevertheless, cyclol bonds were identified in small, naturally occurring cyclic peptides in the 1950s.
Clarification of the modern terminology is appropriate. The classic cyclol reaction is the addition of the NH amine of a peptide group to the C=O carbonyl group of another; the resulting compound is now called an azacyclol. By analogy, an oxacyclol is formed when an OH hydroxyl group is added to a peptidyl carbonyl group. Likewise, a thiacyclol is formed by adding an SH thiol moiety to a peptidyl carbonyl group.
The oxacyclol alkaloid ergotamine from the fungus Claviceps purpurea was the first identified cyclol. The cyclic depsipeptide serratamolide is also formed by an oxacyclol reaction. Chemically analogous cyclic thiacyclols have also been obtained. Classic azacyclols have been observed in small molecules and tripeptides. Peptides are naturally produced from the reversion of azacylols, a key prediction of the cyclol model. Hundreds of cyclol molecules have now been identified, despite Linus Pauling's calculation that such molecules should not exist because of their unfavorably high energy.
After a long hiatus during which she worked mainly on the mathematics of X-ray crystallography, Wrinch responded to these discoveries with renewed enthusiasm for the cyclol model and its relevance in biochemistry. She also published two books describing the cyclol theory and small peptides in general.
Illustration of the scientific method
The cyclol model of protein structure is an example of empirical falsifiability acting as part of the scientific method. An original hypothesis is made that accounts for unexplained experimental observations; the consequences of this hypothesis are worked out, leading to predictions that are tested by experiment. In this case, the key hypothesis was that the cyclol form of the peptide group could be favored over the amide form. This hypothesis led to the predictions of the cyclol-6 molecule and the cyclol fabric, which in turn suggested the model of semi-regular polyhedra for globular proteins. A key testable prediction was that a folded protein's carbonyl groups should be largely converted to hydroxyl groups; however, spectroscopic and chemical experiments showed that this prediction was incorrect. The cyclol model also predicts a high lateral density of amino acids in folded proteins and in films that does not agree with experiment. Hence, the cyclol model could be rejected and the search begun for new hypotheses of protein structure, such as the models of the alpha helix proposed in the 1940s and 1950s.
It is sometimes argued that the cyclol hypothesis should never have been advanced, because of its a priori flaws, e.g., its steric clashes, its inability to accommodate proline, and the high free energy disfavoring the cyclol reaction itself. Although such flaws rendered the cyclol hypothesis implausible, they did not make it impossible. The cyclol model was the first well-defined structure proposed for globular proteins, and too little was then known of intramolecular forces and protein structure to reject it immediately. It neatly explained several general properties of proteins and accounted for then-anomalous experimental observations. Although generally incorrect, some elements of the cyclol theory were eventually verified, such as the cyclol reactions and the role of hydrophobic interactions in protein folding. A useful comparison is the Bohr model of the hydrogen atom, which was considered implausible from its inception, even by its creator, yet led the way to the ultimately correct theory of quantum mechanics. Similarly, Linus Pauling proposed a well-defined model of DNA that was likewise implausible yet thought-provoking to other investigators.
Conversely, the cyclol model is an example of an incorrect scientific theory of great symmetry and beauty, two qualities that can be regarded as signs of "obviously true" scientific theories. For example, the Watson-Crick double helix model of DNA is sometimes said to be "obvious" because of its plausible hydrogen bonding and symmetry; nevertheless, other, less symmetrical structures of DNA are favored under different conditions. Similarly, the beautiful theory of general relativity was considered by Albert Einstein as not needing experimental verification; yet even this theory will require revision for consistency with quantum field theory.
- Tiselius, A (1939). "The Chemistry of Proteins and Amino Acids". Annual Review of Biochemistry 8: 155–184. doi:10.1146/annurev.bi.08.070139.001103.
- Svedberg, T (1929). "Mass and size of protein molecules". Nature 123 (3110): 871. Bibcode:1929Natur.123..871S. doi:10.1038/123871a0.
- Svedberg, T (1934). "Sedimentation of molecules in centrifugal fields". Chemical Reviews 14: 1–15. doi:10.1021/cr60047a001.
- Bergmann, M; Niemann C (1937). "On the structure of proteins: cattle hemoglobin, egg albumin, cattle fibrin, and gelatin". Journal of Biological Chemistry 118: 301–314.
- Svedberg, T (1930). "The pH Stability Regions of Proteins". Transactions of the Faraday Society 26: 741–744.
- Fruton, JS (1979). "Early theories of protein structure". Annals of the New York Academy of Sciences 325: 1–18. Bibcode:1979NYASA.325....1F. doi:10.1111/j.1749-6632.1979.tb14125.x. PMID 378063.
- Hofmeister, F (1902). "Über Bau und Gruppierung der Eiweisskörper". Ergebnisse der Physiologie 1: 759–802. doi:10.1007/BF02323641.
- Fischer, E (1902). "Über die Hydrolyse der Proteinstoffe". Chemiker Zeitung 26: 939–940.
- Fischer, E (1913). "Synthese von Depsiden, Flechtenstoffen und Gerbstoffen". Berichte der deutschen chemischen Gesellschaft 46 (3): 3253–3289. doi:10.1002/cber.191304603109.
- Sørensen, SPL (1930). "The constitution of soluble proteins as reversibly dissociable component systems". Comptes rendus des travaux du Laboratoire Carlsberg 18: 1–124.
- Fruton, JS (1999). Proteins, Enzymes, Genes: The Interplay of Chemistry and Biology. New Haven, CT: Yale University Press. ISBN 0-585-35980-6.
- Abderhalden, E (1924). "Diketopiperazines". Naturwissenschaften 12: 716. Bibcode:1924NW.....12..716A. doi:10.1007/BF01504819.
- Abderhalden, E; Komm E (1924). "Über die Anhydridstruktur der Proteine". Zeitschrift für physiologische Chemie 139: 181–204. doi:10.1515/bchm2.1924.139.3-4.181.
- Linderstrøm-Lang, K; Hotchkiss RD; Johansen G (1938). "Peptide Bonds in Globular Proteins". Nature 142 (3605): 996. Bibcode:1938Natur.142..996L. doi:10.1038/142996a0.
- Chick, H; Martin CJ (1910). "On the "Heat" Coagulation of Proteins". Journal of Physiology 40: 404–430.
Chick, H; Martin CJ (1911). "On the "Heat" Coagulation of Proteins. II. The Action of Hot Water upon Egg-albumen and the Influence of Acid and Salts upon Reaction Velocity". Journal of Physiology 43: 1–27.
Chick, H; Martin CJ (1912). "On the "Heat" Coagulation of Proteins. III. The Influence of Alkali upon Reaction Velocity". Journal of Physiology 45: 61–69.
Chick, H; Martin CJ (1912). "On the "Heat" Coagulation of Proteins. IV. The Conditions controlling the Agglutination of Proteins already acted upon by Hot Water". Journal of Physiology 45: 261–295.
- Anson, ML; Mirsky AE (1929). "Protein Coagulation and Its Reversal". Journal of General Physiology 13: 121–132.
- Anson, ML (1945). "Protein Denaturation and the Properties of Protein Groups". Advances in Protein Chemistry. Advances in Protein Chemistry 2: 361–386. doi:10.1016/S0065-3233(08)60629-4. ISBN 978-0-12-034202-0.
- Wu, H (1931). "Studies on Denaturation of Proteins. XIII. A Theory of Denaturation". Chinese Journal of Physiology 5: 321–344. Preliminary reports were presented before the XIIIth International Congress of Physiology at Boston (19–24 August 1929) and in the October 1929 issue of the American Journal of Physiology.
- Mirsky, AE; Pauling L (1936). "On the Structure of Native, Denatured, and Coagulated Proteins". Proceedings of the National Academy of Sciences of the United States of America 22 (7): 439–447. Bibcode:1936PNAS...22..439M. doi:10.1073/pnas.22.7.439.
- Neurath, H; Greenstein JP; Putnam FW; Erickson JO (1944). "The Chemistry of Protein Denaturation". Chemical Reviews 34 (2): 157–265. doi:10.1021/cr60108a003.
- Putnam, F (1953). "Protein Denaturation". The Proteins (H. Neurath and K. Bailey, eds.) 1B: 807–892.
- Astbury, WT; Woods HJ (1931). "The Molecular Weight of Proteins". Nature 127 (3209): 663–665. Bibcode:1931Natur.127..663A. doi:10.1038/127663b0.
- Astbury, WT (1933). "Some Problems in the X-Ray Analysis of the Structure of Animal Hairs and Other Protein Fibres". Transactions of the Faraday Society 29 (140): 193–211. doi:10.1039/tf9332900193.
- Jordan Lloyd, D (1932). "Colloidal Structure and its Biological Significance". Biological Review 7: 254–273. doi:10.1111/j.1469-185x.1962.tb01043.x.
- Jordan Lloyd, D; Marriott (1933). "Title unknown". Transactions of the Faraday Society 29: 1228. doi:10.1039/tf9332901228.
- Astbury, WT (1936). "Unknown title". Journal of the Textile Institute 27: 282–?.
- Wrinch, DM (1936). "The Pattern of Proteins". Nature 137 (3462): 411–412. Bibcode:1936Natur.137..411W. doi:10.1038/137411a0.
- Wrinch, DM (1936). "Energy of Formation of 'Cyclol' Molecules". Nature 138 (3484): 241–242. Bibcode:1936Natur.138..241W. doi:10.1038/138241a0.
- Frank, FC (1936). "Energy of Formation of 'Cyclol' Molecules". Nature 138 (3484): 242. Bibcode:1936Natur.138..242F. doi:10.1038/138242a0.
- Langmuir, I; Wrinch DM (1939). "Nature of the Cyclol Bond". Nature 143 (3611): 49–52. Bibcode:1939Natur.143...49L. doi:10.1038/143049a0.
- Langmuir, I (1939). "The Structure of Proteins". Proceedings of the Physical Society 51 (4): 592–612. Bibcode:1939PPS....51..592L. doi:10.1088/0959-5309/51/4/305.
- Wrinch, DM (1938). "On the Hydration and Denaturation of Proteins". Philosophical Magazine 25: 705–739.
- Wrinch, DM (1936). "Hydration and Denaturation of Proteins". Nature 142 (3588): 260. Bibcode:1938Natur.142..259.. doi:10.1038/142259a0.
- Dow, RB; Matthews JE; Jr. and Thorp WTS (1940). "The Effect of High Pressure Treatment on the Physiological Activity of Insulin". American Journal of Physiology 131: 382–387.
- Kauzmann, W (1959). "Some Factors in the Interpretation of Protein Denaturation". Advances in Protein Chemistry. Advances in Protein Chemistry 14: 1–63. doi:10.1016/S0065-3233(08)60608-7. ISBN 978-0-12-034214-3. PMID 14404936.
- Wrinch, DM (1936). "Structure of Proteins and of Certain Physiologically Active Compounds". Nature 138 (3493): 651–652. Bibcode:1936Natur.138..651W. doi:10.1038/138651a0.
- Wrinch, DM; Jordan Lloyd D (1936). "The Hydrogen Bond and the Structure of Proteins". Nature 138 (3496): 758–759. Bibcode:1936Natur.138..758W. doi:10.1038/138758a0.
- Wrinch, DM (1937). "Nature of the Linkage in Proteins". Nature 139 (3521): 718. Bibcode:1937Natur.139..718W. doi:10.1038/139718a0.
- Astbury, WT; Wrinch DM (1937). "Intramolecular Folding of Proteins by Keto-Enol Interchange". Nature 139 (3523): 798. Bibcode:1937Natur.139..798A. doi:10.1038/139798a0.
- Wrinch, D. "The Fabric Theory of Protein Structure". Philosophical Magazine 30: 64–67.
- Wrinch, DM (1937). "The Cyclol Theory and the 'Globular' Proteins". Nature 139 (3527): 972–973. Bibcode:1937Natur.139..972W. doi:10.1038/139972a0.
- Wrinch, DM (1947). "The Native Protein". Science 106 (2743): 73–76. Bibcode:1947Sci...106...73W. doi:10.1126/science.106.2743.73. PMID 17808858.
- Wrinch, DM (1937). "On the Pattern of Proteins". Proceedings of the Royal Society A160: 59–86.
Wrinch, DM (1937). "The Cyclol Hypothesis and the "Globular" Proteins". Proceedings of the Royal Society A161: 505–524.
Wrinch, DM (1938). "On the Molecular Weights of the Globular Proteins". Philosophical Magazine 26: 313–332.
- Wrinch, DM (1939). "The Tuberculin Protein TBU-Bovine (523)". Nature 144 (3636): 77. Bibcode:1939Natur.144...77W. doi:10.1038/144077a0.
- Wrinch, DM (1937). "On the structure of pepsin". Philosophical Magazine 24: 940.
- Wrinch, DM (1938). "Structure of Pepsin". Nature 142 (3587): 217. Bibcode:1938Natur.142..215.. doi:10.1038/142215a0.
- Wrinch, DM (1937). "On the Structure of Insulin". Science 85 (2215): 566–567. Bibcode:1937Sci....85..566W. doi:10.1126/science.85.2215.566. PMID 17769864.
Wrinch, DM (1937). "On the Structure of Insulin". Transactions of the Faraday Society 33: 1368–1380. doi:10.1039/tf9373301368.
Wrinch, DM (1938). "The Structure of the Insulin Molecule". Journal of the American Chemical Society 60 (8): 2005–2006. doi:10.1021/ja01275a514.
Wrinch, DM (1938). "The Structure of the Insulin Molecule". Science 88 (2276): 148–149. Bibcode:1938Sci....88..148W. doi:10.1126/science.88.2276.148-a. PMID 17751525.
Wrinch, DM; Langmuir I (1938). "The Structure of the Insulin Molecule". Journal of the American Chemical Society 60 (9): 2247–2255. doi:10.1021/ja01276a062.
Langmuir, I; Wrinch DM (1939). "A Note on the Structure of Insulin". Proceedings of the Physical Society 51 (4): 613–624. Bibcode:1939PPS....51..613L. doi:10.1088/0959-5309/51/4/306.
- Bragg, WL (1939). "Patterson Diagrams in Crystal Analysis". Nature 143 (3611): 73–74. Bibcode:1939Natur.143...73B. doi:10.1038/143073a0.
Bernal, JD (1939). "Vector Maps and the Cyclol Hypothesis". Nature 143 (3611): 74–75. Bibcode:1939Natur.143...74B. doi:10.1038/143074a0.
Robertson, JM (1939). "Vector Maps and Heavy Atoms in Crystal Analysis and the Insulin Structure". Nature 143 (3611): 75–76. Bibcode:1939Natur.143...75R. doi:10.1038/143075a0.
- Riley, DP; Fankuchen I (1939). "A Derived Patterson Analysis of the Skeleton of the Cyclol C2 Molecule". Nature 143 (3624): 648–649. Bibcode:1939Natur.143..648R. doi:10.1038/143648a0.
Wrinch, DM (1940). "Patterson Projection of the Skeletons of the Structure proposed for the Insulin Molecule". Nature 145 (3687): 1018. Bibcode:1940Natur.145.1018W. doi:10.1038/1451018a0.
Riley, D (1940). "A Patterson Analysis derived from the Cyclol C2 Skeleton". Nature 146 (3694): 231. Bibcode:1940Natur.146..231R. doi:10.1038/146231a0.
- Neurath, H; Bull HB (1938). "The Surface Activity of Proteins". Chemical Reviews 23 (3): 391–435. doi:10.1021/cr60076a001.
- Huggins, M (1939). "The Structure of Proteins". Journal of the American Chemical Society 61 (3): 755. doi:10.1021/ja01872a512.
- Haurowitz, F (1938). "The arrangement of peptide chains in sphaero protein-molecules". Zeitschrift der physiologischen Chemie 256: 28–32.
- Meyer, KH; Hohenemser W (1938). "Possibility of the Formation of Cyclols from Simple Peptides". Nature 141 (3582): 1138–1139. Bibcode:1938Natur.141.1138M. doi:10.1038/1411138b0.
- Bergmann, M; Niemann C (1938). "The Chemistry of Amino Acids and Proteins". Annual Reviews in Biochemistry 7: 99–124. doi:10.1146/annurev.bi.07.070138.000531.
- Neuberger, A (1939). "Chemical criticism of the cyclol and frequency hypothesis of protein structure". Proceedings of the Royal Society 170: 64–65.
- Neuberger, A (1939). "Chemical Aspects of the Cyclol Hypothesis". Nature 143 (3620): 473. Bibcode:1939Natur.143..473N. doi:10.1038/143473a0.
- Haurowitz, F; Astrup T (1939). "Ultraviolet absorption of genuine and hydrolysed protein". Nature 143 (3612): 118–119. Bibcode:1939Natur.143..118H. doi:10.1038/143118b0.
- Klotz, IM; Griswold P (1949). "Infrared Spectra and the Amide Linkage in a Native Globular Protein". Science 109 (2830): 309–310. Bibcode:1949Sci...109..309K. doi:10.1126/science.109.2830.309. PMID 17782718.
- Pauling, L; Niemann C (1939). "The Structure of Proteins". Journal of the American Chemical Society 61 (7): 1860–1867. doi:10.1021/ja01876a065.
- Hotchkiss, RD (1939). "The Determination of Peptide Bonds in Crystalline Lactoglobulin". Journal of Biological Chemistry 131: 387–395.
- Wrinch, DM (1941). "The Geometrical Attack on Protein Structure". Journal of the American Chemical Society 63 (2): 330–33. doi:10.1021/ja01847a004.
- Wrinch, DM (1940). "The Cyclol Hypothesis". Nature 145 (3678): 669–670. Bibcode:1940Natur.145..669W. doi:10.1038/145669a0.
- Wrinch, DM (1948). "The Native Proteins as Polycondensations of Amino Acids". Science 107 (2783): 445–446. doi:10.1126/science.107.2783.445-a. PMID 17844448.
- Wrinch, DM (1948). "Skeletal Units in Protein Crystals". Science 115 (2987): 356–357. Bibcode:1952Sci...115..356W. doi:10.1126/science.115.2987.356. PMID 17748855.
- Wrinch, DM (1948). "Molecules of the Insulin Structure". Science 116 (3021): 562–564. Bibcode:1952Sci...116..562W. doi:10.1126/science.116.3021.562.
- Wrinch, DM (1939). "The Structure of the Globular Proteins". Nature 143 (3620): 482–483. Bibcode:1939Natur.143..482W. doi:10.1038/143482a0.
- Wrinch, DM (1939). "The Cyclol Theory and the Structure of Insulin". Nature 143 (3627): 763–764. Bibcode:1939Natur.143..763W. doi:10.1038/143763a0.
- Wrinch, DM (1939). "Native Proteins, Flexible Frameworks and Cytoplasmic Organization". Nature 150 (3800): 270–271. Bibcode:1942Natur.150..270W. doi:10.1038/150270a0.
- Anslow, GA (1942). "Bond Energies in Some Protein Fabrics and Side Chains". Physical Review 61 (7–8): 547. Bibcode:1942PhRv...61..541.. doi:10.1103/PhysRev.61.541.
- Anslow, GA (1945). "Ultraviolet Spectra of Biologically Important Molecules". Journal of Applied Physics 16: 41–49. Bibcode:1945JAP....16...41A. doi:10.1063/1.1707499.
- Anslow, GA (1953). "The Sites of the Amino-Acid Residues on a Cyclol Model of Insulin". Journal of Chemical Physics 21 (11): 2083–2084. Bibcode:1953JChPh..21.2083A. doi:10.1063/1.1698765.
- Guedez, T; Núñez A; Tineo E; Núñez O (2002). "Ring size configuration effect and the transannular intrinsic rates in bislactam macrocycles". Journal of the Chemical Society, Perkin Transactions 2 2002 (12): 2078–2082. doi:10.1039/b207233e.
- Bernal, JD (1939). "Structure of proteins". Nature 143 (3625): 663–667. Bibcode:1939Natur.143..663B. doi:10.1038/143663a0.
- Wieland T and Bodanszky M, The World of Peptides, Springer Verlag, pp.193–198. ISBN 0-387-52830-X
- Hofmann, A; Ott H; Griot R; Stadler PA; Frey AJ (1963). "Synthese von Ergotamin". Helvetica Chimica Acta 46: 2306–2336.
- Shemyakin, MM; Antonov VK; Shkrob AM (1963). "Activation of the amide group by acylation". Peptides, Proc. 6th Europ. Pept. Symp., Athens: 319–328.
- Zanotti, G; Pinnen F; Lucente G; Cerrini S; Fedeli W; Mazza F (1984). "Peptide thiacyclols. Synthesis and structural studies". J. Chem. Soc. Perkin Trans. 1: 1153–1157. doi:10.1039/p19840001153.
- Griot, RG; Frey AJ (1963). "The formation of cyclols from N-hydroxyacyl lactames". Tetrahedron 19 (11): 1661–1673. doi:10.1016/S0040-4020(01)99239-7.
- Lucente, G; Romeo A (1971). "Synthesis of cyclols from small peptides via amide-amide reaction". Chem. Commun. ?: 1605–1607. doi:10.1039/c29710001605.
Rothe M, Schindler W, Pudill R, Kostrzewa U, Theyson R, and Steinberger R. (1971) "Zum Problem der Cycloltripeptidsynthese", Peptides, Proc. 11th Europ. Pept. Symp., Wien, 388–399.
Rothe M and Roser KL. (1988) "Conformational flexibility of cyclic tripeptides", Abstr. 20th Europ. Pept. Symp. Tübingen, p. 36.
- Wieland T and Mohr H. (1956) "Diacylamide als energiereiche Verbindungen. Diglycylimid", Liebigs Ann. Chem., 599, 222–232.
Wieland T and Urbach H. (1958) "Weitere Di-Aminoacylimide und ihre intramolekulare Umlagerung", Liebigs Ann. Chem., 613, 84–95.
Brenner, M (1958). Wolstenholme GEW and O'Connor CM, eds., Churchill, ed. "The aminoacyl insertion". Ciba Foundation Symposium on Amino acids and peptides with antimetabolic activity.
- Wrinch, DM (1957). "Structure of Bacitracin A". Nature 179 (4558): 536–537. Bibcode:1957Natur.179..536W. doi:10.1038/179536a0.
Wrinch, DM (1957). "An Approach to the Synthesis of Polycyclic Peptides". Nature 180 (4584): 502–503. Bibcode:1957Natur.180..502W. doi:10.1038/180502b0.
Wrinch, DM (1962). "Some Issues in Molecular Biology and Recent Advances in the Organic Chemistry of Small Peptides". Nature 193 (4812): 245–247. Bibcode:1962Natur.193..245W. doi:10.1038/193245a0. PMID 14008494.
Wrinch, DM (1963). "Recent Advances in Cyclol Chemistry". Nature 199 (4893): 564–566. Bibcode:1963Natur.199..564W. doi:10.1038/199564a0.
Wrinch, DM (1965). "A Contemporary Picture of the Chemical Aspects of Polypeptide Chain Structures and Certain Problems of Molecular Biology". Nature 206 (4983): 459–461. Bibcode:1965Natur.206..459W. doi:10.1038/206459a0. PMID 5319104.
- Wrinch, DM (1960). Chemical Aspects of the Structures of Small Peptides: An Introduction. Copenhagen: Munksgaard.
- Wrinch, DM (1965). Chemical Aspects of Polypeptide Chain Structures and the Cyclol Theory. New York: Plenum Press.
- Kauzmann, W (1993). "Reminiscences from a life in protein physical chemistry". Protein Science 2 (4): 671–691. doi:10.1002/pro.5560020418. PMC 2142355. PMID 8518739.
- Tanford, C; Reynolds J (2001). Nature's robots: A history of proteins. Oxford: Oxford University Press. ISBN 0-19-850466-7.
- Pais, A (1986). Inward Bound: Of Matter and Forces in the Physical World. Oxford University Press. ISBN 0-19-851971-0.
Bohr, N (1913). "On the Constitution of Atoms and Molecules (Part 1 of 3)". Philosophical Magazine 26: 1–25. doi:10.1080/14786441308634955.
Bohr, N (1913). "On the Constitution of Atoms and Molecules, Part II Systems Containing Only a Single Nucleus". Philosophical Magazine 26 (153): 476–502. doi:10.1080/14786441308634993.
Bohr, N (1913). "On the Constitution of Atoms and Molecules, Part III". Philosophical Magazine 26: 857–875. doi:10.1080/14786441308635031.
Bohr, N (1914). "The spectra of helium and hydrogen". Nature 92 (2295): 231–232. Bibcode:1913Natur..92..231B. doi:10.1038/092231d0.
- Pauling, L; Corey RB (1953). "A Proposed Structure For The Nucleic Acids". Proceedings of the National Academy of Sciences 39 (2): 84–97. Bibcode:1953PNAS...39...84P. doi:10.1073/pnas.39.2.84. PMC 1063734. PMID 16578429.
- Franklin, RE; Gosling R (1953). "Molecular configuration of sodium thymonucleate". Nature 171 (4356): 740–741. Bibcode:1953Natur.171..740F. doi:10.1038/171740a0. PMID 13054694.
- Watson, JD; Crick F (1953). "Molecular structure of nucleic acids: A structure for deoxyribonucleic acid". Nature 171 (4356): 737–738. Bibcode:1953Natur.171..737W. doi:10.1038/171737a0. PMID 13054692.
- Saenger, W (1988). Principles of Nucleic Acid Structure. Springer Verlag. ISBN 0-387-90762-9.
- Pais, A. (1982). Subtle is the Lord: The Science and the Life of Albert Einstein. Oxford University Press. ISBN 0-19-853907-X.
- "Protein Units Put in Graphic 'Cage'", New York Times, 19 April 1940: 14.
- "Waffle-Iron Theory of Proteins", New York Times, 2 February 1947: E9.
- Senechal, Marjorie, ed. (1980), Structures of Matter and Patterns in Science, inspired by the work and life of Dorothy Wrinch, 1894–1976: Proceedings of a Symposium held at Smith College, Northampton, Massachusetts on 28–30 September 1977, Schenkman Publishing Company.
- "Selected papers of Dorothy Wrinch, from the Sophia Smith Collection", in Structures of Matter and Patterns in Science.
- Senechal, Marjorie (2013), I Died For Beauty: Dorothy Wrinch and the Cultures of Science, Oxford University Press.