List of biophysically important macromolecular crystal structures

Myoglobin sketch

Alpha helix

1960 - Myoglobin was the very first high-resolution crystal structure of a protein molecule.[2] Myoglobin cradles an iron-containing heme group that reversibly binds oxygen for use in powering muscle fibers, and those first crystals were of myoglobin from the sperm whale, whose muscles need copious oxygen storage for deep dives. The myoglobin 3-dimensional structure is made up of 8 alpha-helices, and the crystal structure showed that their conformation was right-handed and very closely matched the geometry proposed by Linus Pauling, with 3.6 residues per turn and backbone hydrogen bonds from the peptide NH of one residue to the peptide CO of residue i+4. Myoglobin is a model system for many types of biophysical studies,[3] especially involving the binding process of small ligands such as oxygen and carbon monoxide.

Hemoglobin beta chain

Hemoglobin oxy/deoxy transition

1960 - The Hemoglobin crystal structure[4] showed a tetramer of two related chain types and was solved at much lower resolution than the monomeric myoglobin, but it clearly had the same basic 8-helix architecture (now called the "globin fold"). Further hemoglobin crystal structures at higher resolution [PDB 1MHB, 1DHB) soon showed the coupled change of both local and quaternary conformation between the oxy and deoxy states of hemoglobin,[5] which explains the cooperativity of oxygen binding in the blood and the allosteric effect of factors such as pH and DPG. For decades hemoglobin was the primary teaching example for the concept of allostery, as well as being an intensive focus of research and discussion on allostery. In 1909, hemoglobin crystals from >100 species were used to relate taxonomy to molecular properties.[6] That book was cited by Perutz in the 1938 report[7] of horse hemoglobin crystals that began his long saga to solve the crystal structure. Hemoglobin crystals are pleochroic - dark red in two directions and pale red in the third[6] - because of the orientation of the hemes, and the bright Soret band of the heme porphyrin groups is used in spectroscopic analysis of hemoglobin ligand binding.

HEW lysozyme ribbon

1965 - Hen-egg-white lysozyme (PDB file 1lyz).[8] was the first crystal structure of an enzyme (it cleaves small carbohydrates into simple sugars), used for early studies of enzyme mechanism.[9] It contained beta sheet (antiparallel) as well as helices, and was also the first macromolecular structure to have its atomic coordinates refined (in real space).[10] The starting material for preparation can be bought at the grocery store, and hen-egg lysozyme crystallizes very readily in many different space groups; it is the favorite test case for new crystallographic experiments and instruments. Recent examples are nanocrystals of lysozyme for free-electron laser data collection[11] and microcrystals for micro electron diffraction.[12]

Ribonuclease A ribbon drawing

1967 - Ribonuclease A (PDB file 2RSA)[13] is an RNA-cleaving enzyme stabilized by 4 disulfide bonds. It was used in Anfinsen's seminal research on protein folding which led to the concept that a protein's 3-dimensional structure was determined by its amino-acid sequence. Ribonuclease S, the cleaved, two-component form studied by Fred Richards, was also enzymatically active, had a nearly identical crystal structure (PDB file 1RNS),[14] and was shown to be catalytically active even in the crystal,[15] helping dispel doubts about the relevance of protein crystal structures to biological function.

Two domains of elastase

1967 - The serine proteases are a historically very important group of enzyme structures, because collectively they illuminated catalytic mechanism (in their case, by the Ser-His-Asp "catalytic triad"), the basis of differing substrate specificities, and the activation mechanism by which a controlled enzymatic cleavage buries the new chain end to properly rearrange the active site.[16] The early crystal structures included chymotrypsin (PDB file 2CHA),[17] chymotrypsinogen (PDB file 1CHG),[18] trypsin (PDB file 1PTN),[19] and elastase (PDB file 1EST).[20] They also were the first protein structures that showed two near-identical domains, presumably related by gene duplication. One reason for their wide use as textbook and classroom examples was the insertion-code numbering system (hated by all computer programmers), which made Ser195 and His57 consistent and memorable despite the protein-specific sequence differences.

1968 - Papain

Carboxypeptidase, with Zn

CPA inhibitor

1969 - Carboxypeptidase A is a zinc metalloprotease. Its crystal structure (PDB file 1CPA)[21] showed the first parallel beta structure: a large, twisted, central sheet of 8 strands with the active-site Zn located at the C-terminal end of the middle strands and the sheet flanked on both sides with alpha helices. It is an exopeptidase that cleaves peptides or proteins from the carboxy-terminal end rather than internal to the sequence. Later a small protein inhibitor of carboxypeptidase was solved (PDB file 4CPA)[22] that mechanically stops the catalysis by presenting its C-terminal end just sticking out from between a ring of disulfide bonds with tight structure behind it, preventing the enzyme from sucking in the chain past the first residue.

Subtilisin ribbon

1969 - Subtilisin (PDB file 1sbt [23]) was a second type of serine protease with a near-identical active site to the trypsin family of enzymes, but with a completely different overall fold. This gave the first view of convergent evolution at the atomic level. Later, an intensive mutational study on subtilisin documented the effects of all 19 other amino acids at each individual position.[24]

1970 - Lactate dehydrogenase

Commputer ribbon, with 3 SS

1970 - Basic pancreatic trypsin inhibitor, or BPTI (PDB file 2pti[25]), is a small, very stable protein that has been a highly productive model system for study of super-tight binding, disulfide bond (SS) formation, protein folding, molecular stability by amino-acid mutations or hydrogen-deuterium exchange, and fast local dynamics by NMR. Biologically, BPTI binds and inhibits trypsin while stored in the pancreas, allowing activation of protein digestion only after trypsin is released into the stomach.

Rubredoxin with nn-heme iron

1970 - Rubredoxin (PDB file 2rxn[26]) was the first redox structure solved, a minimalist protein with the iron bound by 4 Cys sidechains from 2 loops at the top of β hairpins. It diffracted to 1.2Å, enabling the first reciprocal-space refinement of a protein (4,5rxn[27]). [NB: beware 4rxn, done without geometry restraints!] Archaeal rubredoxins account for many of the highest-resolution small structures in the PDB.

SS-linked insulin monomer

Space-grown insulin crystals

1971 - Insulin (PDB file 1INS)[28] is a hormone central to the metabolism of sugar and fat storage, and important in human diseases such as obesity and diabetes. It is biophysically notable for its Zn binding, its equilibrium between monomer, dimer, and hexamer states, its ability to form crystals in vivo, and its synthesis as a longer "pro" form which is then cleaved to fold up as the active 2-chain, SS-linked monomer. Insulin was a success of NASA's crystal-growth program on the space shuttle, producing bulk preparations of very uniform tiny crystals for controlled dosage.

1971 - Staphylococcal nuclease

1971 - Cytochrome C

1974 - T4 phage lysozyme

1974 - Immunoglobulins

1975 - Cu,Zn Superoxide dismutase

1976 - Transfer RNA

TIM ribbon drawing, PDB 1tim

1976 - Triose phosphate isomerase

1976 - Rhizopuspepsin

1976 - Endothiapepsin

1976 - Penicillopepsin

1978 - Icosahedral virus

1981 - Dickerson B-form DNA dodecamer

1981 - Crambin

1985 - Calmodulin

1985 - DNA polymerase

Photosynthetic reaction center in membrane

1985 - Photosynthetic reaction center Pairs of bacteriochlorophylls (green) inside the membrane capture energy from sunlight, then traveling by many steps to become available at the heme groups (red) in the cytochrome-C module at the top. This was first crystal structure solved for a membrane protein, a milestone recognized by a Nobel Prize to Hartmut Michel, Hans Deisenhofer, and Robert Huber.

CAP protein dimer on DNA, PDB 1cgp

1986 - Repressor/DNA interactions

1987 Major histocompatibility complex'

1987 Ubiquitin

1987 ROP protein

1989 HIV-1 protease

1990 Bacteriorhodopsin

1991 GCN4 coiled coil

1991 HIV-1 reverse transcriptase

1993 Beta helix of Pectate lyase

1994 Collagen

1994 Barnase/barstar complex

1994 F1 ATPase

1995 Heterotrimeric G proteins

1996 Green fluorescent protein

1996 CDK/cyclin complex

Kinesin dimer, PDB 3kin

1996 - Kinesin motor protein

1997 GroEL/ES chaperone

1997 Nucleosome

1998 Group I self-splicing intron

Topoisomerase I on DNA (by David Goodsell)

1998 - DNA topoisomerases perform the biologically important and necessary job of untangling DNA strands or helices that get entwined with each other or twisted too tightly during normal cellular processes such as the transcription of genetic information.

1998 Tubulin alpha/beta dimer

1998 Potassium channel

1998 Holliday junction

2000 Ribosome

2000 AAA+ ATPase

2002 Ankyrin repeats

2003 TOP7 protein design

2004 Cyanobacterial Circadian clock proteins

2004 Riboswitch

2006 Human exosome

beta-adrenergic receptor & G protein

2007 G-protein-coupled receptor

Half of a vault particle

2009 The Vault particle is an intriguing new discovery of a large hollow particle common in cells, with several different suggestions for its possible biological function. The crystal structures (PDB files 2zuo, 2zv4, 2zv5[29] and 4hl8[30]) show that each half of the vault is made up of 39 copies of a long 12-domain protein that swirl together to form the enclosure. Disorder at the very top and bottom ends suggests openings for possible access to the interior of the vault.

Photosystem II

2010 - Free-electron laser crystallography