Back

Deciphering the orthorhombic crystal structure of a novel NEIL1 nanobody with pseudo-merohedral twinning

Thompson, M. K.; Sharma, N.; Prakash, A.

2023-08-07 biochemistry
10.1101/2023.08.07.552313 bioRxiv
Show abstract

Nanobodies or VHHs (Variable Heavy domains of Heavy chain) are single domain antibodies that comprise three antigenic complementary determining regions (CDR). Nanobodies are used in numerous scientific applications including, bio-imaging, diagnosis, therapeutics, and macromolecular crystallography. We obtained crystals of a [~]14 kDa nanobody specific for the NEIL1 DNA glycosylase (hereafter called A5) in 0.5 M ammonium sulfate, 0.1 M sodium citrate tribasic dihydrate pH 5.6, and 1.0 M lithium sulfate monohydrate from the Crystal HT Hampton Research screen that were further optimized. Here, we describe the structure determination and refinement of the A5 crystals to a resolution of 2.1 [A]. The data collected were complicated by the presence of anisotropy and twinning, and while initial space group determination pointed to a higher apparent tetragonal crystal system, the data statistics suggested twinning, placing the crystal in an orthorhombic system. Twinning was confirmed by the Padilla and Yeates test, H-test, and Britton test based on local intensity differences with a twin fraction of 0.4. Molecular replacement produced the best solution in the orthorhombic space group P21212 with four molecules in the asymmetric unit and we were able to model over 96% of the residues in the electron density with a final Rwork and Rfree of 0.1988 and 0.2289 upon refinement. SynopsisThe crystal structure of a specific nanobody against NEIL1 was determined to 2.1 [A]. The structure was ultimately solved in an orthorhombic space group after diffraction data analysis revealed mild anisotropy as well as pseudo-merohedral twinning

Matching journals

The top 4 journals account for 50% of the predicted probability mass.

1
Structure
193 papers in training set
Top 0.1%
26.3%
2
Protein Science
246 papers in training set
Top 0.1%
15.0%
3
Acta Crystallographica Section D Structural Biology
59 papers in training set
Top 0.1%
7.2%
4
Scientific Reports
3612 papers in training set
Top 13%
6.2%
50% of probability mass above
5
Communications Biology
993 papers in training set
Top 4%
4.0%
6
Proteins: Structure, Function, and Bioinformatics
88 papers in training set
Top 0.3%
4.0%
7
IUCrJ
32 papers in training set
Top 0.1%
4.0%
8
Nature Communications
5641 papers in training set
Top 34%
3.5%
9
Biochemistry
148 papers in training set
Top 0.7%
3.2%
10
Proceedings of the National Academy of Sciences
2444 papers in training set
Top 19%
2.7%
11
eLife
5828 papers in training set
Top 44%
2.1%
12
ACS Omega
105 papers in training set
Top 1%
1.9%
13
Scientific Data
209 papers in training set
Top 2%
1.7%
14
Journal of Molecular Biology
232 papers in training set
Top 2%
1.7%
15
Nature Structural & Molecular Biology
218 papers in training set
Top 2%
1.5%
16
Journal of Biological Chemistry
690 papers in training set
Top 6%
1.5%
17
The Journal of Physical Chemistry B
167 papers in training set
Top 1%
1.4%
18
Frontiers in Molecular Biosciences
102 papers in training set
Top 2%
1.0%
19
ACS Chemical Biology
167 papers in training set
Top 2%
1.0%
20
Nature
645 papers in training set
Top 10%
0.9%
21
mAbs
32 papers in training set
Top 0.5%
0.8%
22
ACS Bio & Med Chem Au
11 papers in training set
Top 0.1%
0.6%
23
Nature Methods
385 papers in training set
Top 7%
0.6%
24
Journal of Structural Biology
64 papers in training set
Top 0.9%
0.6%